| Year |
Citation |
Score |
| 1990 |
Bianchi DW, Flint AF, Pizzimenti MF, Knoll JH, Latt SA. Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proceedings of the National Academy of Sciences of the United States of America. 87: 3279-83. PMID 2333281 DOI: 10.1073/Pnas.87.9.3279 |
0.424 |
|
| 1989 |
Heartlein MW, Latt SA. Amplified inverted duplications within and adjacent to heterologous selectable DNA. Nucleic Acids Research. 17: 1697-716. PMID 2922290 DOI: 10.1093/Nar/17.4.1697 |
0.42 |
|
| 1989 |
Rudolph NS, Latt SA. Flow cytometric analysis of X-ray sensitivity in ataxia telangiectasia Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 211: 31-41. PMID 2922001 DOI: 10.1016/0027-5107(89)90104-8 |
0.351 |
|
| 1989 |
Rudolph NS, Nagasawa H, Little JB, Latt SA. Identification of ataxia telangiectasia heterozygotes by flow cytometric analysis of X-ray damage Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 211: 19-29. PMID 2922000 DOI: 10.1016/0027-5107(89)90103-6 |
0.34 |
|
| 1989 |
Tantravahi U, Nicholls RD, Stroh H, Ringer S, Neve RL, Kaplan L, Wharton R, Wurster-Hill D, Graham JM, Cantu ES, Frias JL, Kousseff BG, Latt SA. Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome American Journal of Medical Genetics. 33: 78-87. PMID 2750788 DOI: 10.1002/Ajmg.1320330110 |
0.488 |
|
| 1989 |
Simon M, Phillips M, Green H, Stroh H, Glatt K, Burns G, Latt SA. Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP. American Journal of Human Genetics. 45: 910-6. PMID 2574003 |
0.303 |
|
| 1989 |
Nicholls RD, Knoll JH, Glatt K, Hersh JH, Brewster TD, Graham JM, Wurster-Hill D, Wharton R, Latt SA. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome. American Journal of Medical Genetics. 33: 66-77. PMID 2568752 DOI: 10.1002/Ajmg.1320330109 |
0.505 |
|
| 1989 |
Knoll JH, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. American Journal of Medical Genetics. 32: 285-90. PMID 2564739 DOI: 10.1002/Ajmg.1320320235 |
0.487 |
|
| 1988 |
Tantravahi U, Stewart GD, Van Keuren M, McNeil G, Roy S, Patterson D, Drabkin H, Lalande M, Kurnit DM, Latt SA. Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes. Human Genetics. 79: 196-202. PMID 3402991 DOI: 10.1007/Bf00366237 |
0.556 |
|
| 1988 |
Heartlein MW, Knoll JH, Latt SA. Chromosome instability associated with human alphoid DNA transfected into the Chinese hamster genome. Molecular and Cellular Biology. 8: 3611-8. PMID 3221860 DOI: 10.1128/mcb.8.9.3611 |
0.426 |
|
| 1988 |
Covone AE, Kozma R, Johnson PM, Latt SA, Adinolfi M. Analysis of peripheral maternal blood samples for the presence of placenta-derived cells using Y-specific probes and McAb H315. Prenatal Diagnosis. 8: 591-607. PMID 3205864 DOI: 10.1002/Pd.1970080807 |
0.326 |
|
| 1988 |
Tsuji H, Heartlein MW, Latt SA. Disparate effects of 5-bromodeoxyuridine on sister-chromatid exchanges and chromosomal aberrations in Bloom syndrome fibroblasts. Mutation Research. 198: 241-53. PMID 2965297 DOI: 10.1016/0027-5107(88)90061-9 |
0.357 |
|
| 1987 |
Kaplan LC, Wharton R, Elias E, Mandell F, Donlon T, Latt SA. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance. American Journal of Medical Genetics. 28: 45-53. PMID 3674117 DOI: 10.1002/Ajmg.1320280107 |
0.375 |
|
| 1987 |
Shiloh Y, Rose E, Colletti-Feener C, Korf B, Kunkel LM, Latt SA. Rapid cloning of multiple amplified nucleotide sequences from human neuroblastoma cell lines by phenol emulsion competitive DNA reassociation. Gene. 51: 53-9. PMID 3596238 DOI: 10.1016/0378-1119(87)90473-2 |
0.612 |
|
| 1987 |
Bianchi DW, Harris P, Flint A, Latt SA. Direct hybridization to DNA from small numbers of flow-sorted nucleated newborn cells. Cytometry. 8: 197-202. PMID 3582066 DOI: 10.1002/Cyto.990080213 |
0.408 |
|
| 1987 |
Müller U, Donlon TA, Kunkel SM, Lalande M, Latt SA. Y-190, a DNA probe for the sensitive detection of Y-derived marker chromosomes and mosaicism. Human Genetics. 75: 109-13. PMID 3469135 DOI: 10.1007/Bf00591069 |
0.542 |
|
| 1987 |
Kanda N, Tsuchida Y, Hata J, Kohl NE, Alt FW, Latt SA, Utakoji T. Amplification of IMR-32 clones 8, G21, and N-myc in human neuroblastoma xenografts. Cancer Research. 47: 3291-5. PMID 3034408 |
0.309 |
|
| 1987 |
Bruns G, Stroh H, Veldman GM, Latt SA, Floros J. The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10. Human Genetics. 76: 58-62. PMID 3032770 DOI: 10.1007/Bf00283051 |
0.501 |
|
| 1987 |
Harris P, Lalande M, Stroh H, Bruns G, Flint A, Latt SA. Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p. Human Genetics. 77: 95-103. PMID 2888723 DOI: 10.1007/Bf00272372 |
0.462 |
|
| 1987 |
Müller U, Donlon TA, Harris P, Rose E, Hoffman E, Bruns GP, Latt SA. Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18. Cytogenetics and Cell Genetics. 45: 16-20. PMID 2885151 DOI: 10.1159/000132418 |
0.559 |
|
| 1987 |
Müller U, Latt SA, Donlon T. Y-specific DNA sequences in male patients with 46,XX and 47,XXX karyotypes. American Journal of Medical Genetics. 28: 393-401. PMID 2827475 DOI: 10.1002/Ajmg.1320280218 |
0.51 |
|
| 1986 |
Müller U, Lalande M, Donlon T, Latt SA. Moderately repeated DNA sequences specific for the short arm of the human Y chromosome are present in XX males and reduced in copy number in an XY female. Nucleic Acids Research. 14: 1325-40. PMID 3951989 DOI: 10.1093/Nar/14.3.1325 |
0.523 |
|
| 1986 |
Shiloh Y, Korf B, Kohl NE, Sakai K, Brodeur GM, Harris P, Kanda N, Seeger RC, Alt F, Latt SA. Amplification and rearrangement of DNA sequences from the chromosomal region 2p24 in human neuroblastomas. Cancer Research. 46: 5297-301. PMID 3756879 |
0.369 |
|
| 1986 |
Lalande M, Donlon T, Petersen RA, Liberfarb R, Manter S, Latt SA. Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma. Cancer Genetics and Cytogenetics. 23: 151-7. PMID 3756834 |
0.416 |
|
| 1986 |
Latt SA, Shiloh Y, Sakai K, Brodeur G, Donlon T, Korf B, Shipley J, Bruns G, Heartlein M, Kanda N. Novel DNA rearrangement phenomena associated with DNA amplification in human neuroblastomas and neuroblastoma cell lines. Progress in Clinical and Biological Research. 209: 601-12. PMID 3749069 |
0.313 |
|
| 1986 |
Müller U, Donlon T, Schmid M, Fitch N, Richer CL, Lalande M, Latt SA. Deletion mapping of the testis determining locus with DNA probes in 46,XX males and in 46,XY and 46,X,dic(Y) females. Nucleic Acids Research. 14: 6489-505. PMID 3748818 DOI: 10.1093/Nar/14.16.6489 |
0.483 |
|
| 1986 |
Tantravahi U, Bianchi DW, Haley C, Destrempes MM, Ricker AT, Korf BR, Latt SA. Use of Y chromosome specific probes to detect low level sex chromosome mosaicism. Clinical Genetics. 29: 445-8. PMID 3742851 DOI: 10.1111/J.1399-0004.1986.Tb00519.X |
0.514 |
|
| 1986 |
Harris P, Morton CC, Guglielmi P, Li F, Kelly K, Latt SA. Mapping by chromosome sorting of several gene probes, including c-myc, to the derivative chromosomes of a 3;8 translocation associated with familial renal cancer. Cytometry. 7: 589-94. PMID 3536362 DOI: 10.1002/Cyto.990070614 |
0.475 |
|
| 1986 |
Kaplan LC, Wayne A, Crowell S, Latt SA. Trisomy 14 mosaicism in a liveborn male: Clinical report and review of the literature American Journal of Medical Genetics. 23: 925-930. PMID 3515939 DOI: 10.1002/Ajmg.1320230407 |
0.382 |
|
| 1986 |
Latt SA, Lalande M, Donlon T, Wyman A, Rose E, Shiloh Y, Korf B, Müller U, Sakai K, Kanda N. DNA-based detection of chromosome deletion and amplification: diagnostic and mechanistic significance. Cold Spring Harbor Symposia On Quantitative Biology. 51: 299-307. PMID 3472727 DOI: 10.1101/Sqb.1986.051.01.035 |
0.514 |
|
| 1986 |
Fendrock B, Destrempes M, Kaufman RJ, Latt SA. Cytological, flow cytometric, and molecular analysis of the rapid evolution of mammalian chromosomes containing highly amplified DNA sequences. Histochemistry. 84: 121-30. PMID 3086259 DOI: 10.1007/Bf00499822 |
0.523 |
|
| 1986 |
Müller U, Tantravahi U, Monaco A, Stroh H, Kunkel LM, Latt SA. Repeated DNA sequences in the distal long arm of the human X chromosome. Human Genetics. 74: 24-9. PMID 3019869 DOI: 10.1007/Bf00278780 |
0.717 |
|
| 1986 |
Müller U, Lalande M, Disteche CM, Latt SA. Construction, analysis, and application to 46,XY gonadal dysgenesis of a recombinant phage DNA library from flow-sorted human Y chromosomes. Cytometry. 7: 418-24. PMID 3019620 DOI: 10.1002/Cyto.990070505 |
0.537 |
|
| 1986 |
Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, et al. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature. 322: 73-7. PMID 3014348 DOI: 10.1038/322073a0 |
0.609 |
|
| 1986 |
Tantravahi U, Murty VV, Jhanwar SC, Toole JJ, Woozney JM, Chaganti RS, Latt SA. Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis. Cytogenetics and Cell Genetics. 42: 75-9. PMID 3013509 DOI: 10.1159/000132255 |
0.4 |
|
| 1986 |
Donlon TA, Lalande M, Wyman A, Bruns G, Latt SA. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. Proceedings of the National Academy of Sciences of the United States of America. 83: 4408-12. PMID 3012567 DOI: 10.1073/Pnas.83.12.4408 |
0.532 |
|
| 1986 |
Kwan SP, Kunkel L, Bruns G, Wedgwood RJ, Latt S, Rosen FS. Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism Journal of Clinical Investigation. 77: 649-652. PMID 3003164 DOI: 10.1172/Jci112351 |
0.61 |
|
| 1985 |
Shiloh Y, Kanda N, Kunkel LM, Bruns G, Sakai K, Latt SA. Two RFLPs identified by a human chromosome #2 clone at 2p15-2p16 (HGM8 assignment no. D2S5). Nucleic Acids Research. 13: 5403. PMID 4022784 DOI: 10.1093/Nar/13.14.5403 |
0.57 |
|
| 1985 |
Nagasawa H, Latt SA, Lalande ME, Little JB. Effects of X-irradiation on cell-cycle progression, induction of chromosomal aberrations and cell killing in ataxia telangiectasia (AT) fibroblasts. Mutation Research. 148: 71-82. PMID 3969079 DOI: 10.1016/0027-5107(85)90209-X |
0.4 |
|
| 1985 |
Bruns G, Kavathas P, Shiloh Y, Sakai K, Schwaber J, Latt SA, Herzenberg LA. The human T cell antigen Leu-2 (T8) is encoded on chromosome 2. Human Genetics. 70: 311-4. PMID 3926629 DOI: 10.1007/Bf00295366 |
0.471 |
|
| 1985 |
Latt SA, Lalande M, Kunkel LM, Schreck R, Tantravahi U. Applications of fluorescence spectroscopy to molecular cytogenetics. Biopolymers. 24: 77-95. PMID 3886034 DOI: 10.1002/Bip.360240108 |
0.655 |
|
| 1985 |
Ginsburg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA, Orkin SH. Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. Science (New York, N.Y.). 228: 1401-6. PMID 3874428 DOI: 10.1126/Science.3874428 |
0.424 |
|
| 1985 |
Shiloh Y, Shipley J, Brodeur GM, Bruns G, Korf B, Donlon T, Schreck RR, Seeger R, Sakai K, Latt SA. Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines Proceedings of the National Academy of Sciences of the United States of America. 82: 3761-3765. PMID 3858848 DOI: 10.1073/Pnas.82.11.3761 |
0.455 |
|
| 1985 |
Kunkel LM, Monaco AP, Middlesworth W, Ochs HD, Latt SA. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proceedings of the National Academy of Sciences of the United States of America. 82: 4778-82. PMID 2991893 DOI: 10.1073/Pnas.82.14.4778 |
0.72 |
|
| 1985 |
Kunkel LM, Lalande M, Monaco AP, Flint A, Middlesworth W, Latt SA. Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci. Gene. 33: 251-8. PMID 2989089 DOI: 10.1016/0378-1119(85)90232-X |
0.726 |
|
| 1985 |
Kunkel L, Burns G, Aldrige J, Latt S. Genetic analysis of Duchenne dystrophy. Advances in Experimental Medicine and Biology. 182: 287-94. PMID 2988292 DOI: 10.1007/978-1-4684-4907-5_26 |
0.574 |
|
| 1985 |
Sakai K, Kanda N, Shiloh Y, Donlon T, Schreck R, Shipley J, Dryja T, Chaum E, Chaganti RSK, Latt S. Molecular and cytologic analysis of DNA amplification in retinoblastoma Cancer Genetics and Cytogenetics. 17: 95-112. PMID 2986831 DOI: 10.1016/0165-4608(85)90020-2 |
0.465 |
|
| 1985 |
de Martinville B, Kunkel LM, Bruns G, Morlé F, Koenig M, Mandel JL, Horwich A, Latt SA, Gusella JF, Housman D. Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus. American Journal of Human Genetics. 37: 235-49. PMID 2984924 |
0.467 |
|
| 1985 |
Shipley J, Sakai K, Tantravahi U, Fendrock B, Latt SA. Correspondence between effects of 5-azacytidine on SCE formation, cell cycling and DNA methylation in Chinese hamster cells. Mutation Research. 150: 333-45. PMID 2582252 DOI: 10.1016/0027-5107(85)90130-7 |
0.393 |
|
| 1985 |
Lalande M, Schreck RR, Hoffman R, Latt SA. Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis. Cytometry. 6: 1-6. PMID 2578344 DOI: 10.1002/Cyto.990060102 |
0.536 |
|
| 1984 |
Latt SA, Kurnit DM, Bruns GP, Schreck RR, Morton CC, Kunkel LM, Lalande M, Aldridge J, Neve R, Tantravahi U. Molecular genetic approaches to human diseases involving mental retardation. American Journal of Mental Deficiency. 88: 561-71. PMID 6731492 |
0.347 |
|
| 1984 |
Latt SA, Marino M, Lalande M. New fluorochromes, compatible with high wavelength excitation, for flow cytometric analysis of cellular nucleic acids. Cytometry. 5: 339-47. PMID 6468174 DOI: 10.1002/Cyto.990050409 |
0.384 |
|
| 1984 |
Taub R, Kelly K, Battey J, Latt S, Lenoir GM, Tantravahi U, Tu Z, Leder P. A novel alteration in the structure of an activated c-myc gene in a variant t(2;8) Burkitt lymphoma. Cell. 37: 511-20. PMID 6327071 DOI: 10.1016/0092-8674(84)90381-7 |
0.368 |
|
| 1984 |
Kitsiou-Tzeli S, Hallett JJ, Atkins L, Latt SA, Holmes LB. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome. American Journal of Medical Genetics. 18: 725-9. PMID 6237580 DOI: 10.1002/Ajmg.1320180419 |
0.348 |
|
| 1984 |
Lalande M, Kunkel LM, Flint A, Latt SA. Development and use of metaphase chromosome flow-sorting methodology to obtain recombinant phage libraries enriched for parts of the human X chromosome. Cytometry. 5: 101-7. PMID 6232119 DOI: 10.1002/Cyto.990050202 |
0.676 |
|
| 1984 |
Lalande M, Dryja TP, Schreck RR, Shipley J, Flint A, Latt SA. Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus. Cancer Genetics and Cytogenetics. 13: 283-95. PMID 6210139 DOI: 10.1016/0165-4608(84)90073-6 |
0.548 |
|
| 1983 |
Kaufman RJ, Sharp PA, Latt SA. Evolution of chromosomal regions containing transfected and amplified dihydrofolate reductase sequences. Molecular and Cellular Biology. 3: 699-711. PMID 6855772 DOI: 10.1128/Mcb.3.4.699 |
0.464 |
|
| 1983 |
Kunkel LM, Tantravahi U, Kurnit DM, Eisenhard M, Bruns GP, Latt SA. Identification and isolation of transcribed human X chromosome DNA sequences. Nucleic Acids Research. 11: 7961-79. PMID 6689068 DOI: 10.1093/Nar/11.22.7961 |
0.664 |
|
| 1983 |
Kanda N, Schreck R, Alt F, Bruns G, Baltimore D, Latt S. Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 80: 4069-73. PMID 6575396 DOI: 10.1073/Pnas.80.13.4069 |
0.561 |
|
| 1983 |
Tantravahi U, Kirschner DA, Beauregard L, Page L, Kunkel L, Latt S. Cytologic and molecular analysis of 46,XXq- cells to identify a DNA segment that might serve as a probe for a putative human X chromosome inactivation center. Human Genetics. 64: 33-8. PMID 6347866 DOI: 10.1007/Bf00289475 |
0.557 |
|
| 1983 |
Kohl NE, Kanda N, Schreck RR, Bruns G, Latt SA, Gilbert F, Alt FW. Transposition and amplification of oncogene-related sequences in human neuroblastomas Cell. 35: 359-367. PMID 6197179 DOI: 10.1016/0092-8674(83)90169-1 |
0.395 |
|
| 1983 |
D'Andrea AD, Tantravahi U, Lalande M, Perle MA, Latt SA. High resolution analysis of the timing of replication of specific DNA sequences during S phase of mammalian cells. Nucleic Acids Research. 11: 4753-74. PMID 6192392 DOI: 10.1093/Nar/11.14.4753 |
0.406 |
|
| 1982 |
Latt SA, Kaiser TN, Lojewski A, Dougherty C, Juergens L, Brefach S, Sahar E, Gustashaw K, Schreck RR, Powers M, Lalande M. Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemia. Cytogenetics and Cell Genetics. 33: 133-8. PMID 7116934 DOI: 10.1159/000131737 |
0.384 |
|
| 1982 |
Kaiser TN, Lojewski A, Dougherty C, Juergens L, Sahar E, Latt SA. Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment. Cytometry. 2: 291-7. PMID 6804195 DOI: 10.1002/Cyto.990020505 |
0.31 |
|
| 1982 |
Kunkel LM, Tantravahi U, Eisenhard M, Latt SA. Regional localization on the human X of DNA segments cloned from flow sorted chromosomes. Nucleic Acids Research. 10: 1557-78. PMID 6461845 DOI: 10.1093/Nar/10.5.1557 |
0.681 |
|
| 1982 |
Disteche CM, Kunkel LM, Lojewski A, Orkin SH, Eisenhard M, Sahar E, Travis B, Latt SA. Isolation of mouse x-chromosome specific DNA from an x-enriched lambda phage library derived from flow sorted chromosomes. Cytometry. 2: 282-6. PMID 6210515 DOI: 10.1002/Cyto.990020503 |
0.679 |
|
| 1982 |
Sandstrom MM, Beauchesne MT, Gustashaw KM, Latt SA. Chapter 3. Prenatal Cytogenetic Diagnosis Methods in Cell Biology. 26: 35-66. DOI: 10.1016/S0091-679X(08)61363-1 |
0.468 |
|
| 1981 |
Loveday KS, Latt SA. A high buoyant density fraction in mammalian DNA. Characterization and impact on the detection of heteroduplex DNA. Experimental Cell Research. 136: 177-87. PMID 7297610 DOI: 10.1016/0014-4827(81)90049-5 |
0.408 |
|
| 1981 |
Disteche CM, Eicher EM, Latt SA. Late replication patterns in adult and embryonic mice carrying Searle's X-autosome translocation Experimental Cell Research. 133: 357-362. PMID 7238606 DOI: 10.1016/0014-4827(81)90328-1 |
0.483 |
|
| 1981 |
Sahar E, Kittrel C, Fulghum S, Feld M, Latt SA. Sister-chromatid exchange induction in Chinese hamster ovary cells by 8-methoxypsoralen and brief pulses of laser light: assessment of the relative importance of 8-methoxypsoralen--DNA monoadducts and crosslinks. Mutation Research. 83: 91-105. PMID 7196990 DOI: 10.1016/0027-5107(81)90074-9 |
0.341 |
|
| 1981 |
Disteche CM, Carrano AV, Ashworth LK, Burkhart-Schultz K, Latt SA. Flow sorting of the mouse Cattanach X chromosome, T (X; 7) 1 Ct, in an active or inactive state. Cytogenetics and Cell Genetics. 29: 189-97. PMID 7016465 DOI: 10.1159/000131569 |
0.487 |
|
| 1981 |
Latt SA, Barell EF, Dougherty CP, Lazarus H. Patterns of late replication in X chromosomes of human lymphoid cells. Cancer Genetics and Cytogenetics. 3: 171-81. PMID 6974041 DOI: 10.1016/0165-4608(81)90073-X |
0.399 |
|
| 1980 |
Cassel DM, Latt SA. Relationship between DNA adduct formation and sister chromatid exchange induction by [3H]8-methoxypsoralen in Chinese hamster ovary cells. Experimental Cell Research. 128: 15-22. PMID 7408979 DOI: 10.1016/0014-4827(80)90381-X |
0.422 |
|
| 1980 |
Davidson RL, Kaufman ER, Dougherty CP, Ouellette AM, DiFolco CM, Latt SA. Induction of sister chromatid exchanges by BUdR is largely independent of the BUdR content of DNA. Nature. 284: 74-6. PMID 7354875 DOI: 10.1038/284074A0 |
0.397 |
|
| 1980 |
Latt SA, Schreck RR. Sister chromatid exchange analysis American Journal of Human Genetics. 32: 297-313. PMID 6992563 |
0.371 |
|
| 1980 |
Latt SA, Sahar E, Eisenhard ME, Juergens LA. Interactions between pairs of DNA-binding dyes: results and implications of chromosome analysis. Cytometry. 1: 2-12. PMID 6168450 DOI: 10.1002/Cyto.990010103 |
0.489 |
|
| 1980 |
Sahar E, Latt SA. Energy transfer and binding competition between dyes used to enhance staining differentiation in metaphase chromosomes. Chromosoma. 79: 1-28. PMID 6156806 DOI: 10.1007/Bf00328469 |
0.422 |
|
| 1980 |
Latt SA, Schreck RR, Loveday KS, Dougherty CP, Shuler CF. Sister chromatid exchanges Advances in Human Genetics. 10: 267-331. PMID 6156589 DOI: 10.1007/978-1-4615-8288-5_4 |
0.471 |
|
| 1980 |
Latt SA, Juergens LA, Matthews DJ, Gustashaw KM, Sahar E. Energy transfer-enhanced chromosome banding. An overview Cancer Genetics and Cytogenetics. 1: 187-196. DOI: 10.1016/0165-4608(80)90015-1 |
0.426 |
|
| 1979 |
Arndt-Jovin DJ, Latt SA, Striker G, Jovin TM. Fluorescence decay analysis in solution and in a microscope of DNA and chromosomes stained with quinacrine Journal of Histochemistry and Cytochemistry. 27: 87-95. PMID 438507 DOI: 10.1177/27.1.438507 |
0.332 |
|
| 1979 |
Disteche CM, Eicher EM, Latt SA. Late replication in an X-autosome translocation in the mouse: Correlation with genetic inactivation and evidence for selective effects during embryogenesis Proceedings of the National Academy of Sciences of the United States of America. 76: 5234-5238. PMID 291940 DOI: 10.1073/Pnas.76.10.5234 |
0.43 |
|
| 1979 |
Latt SA, Sahar E, Eisenhard ME. Pairs of fluorescent dyes as probes of DNA and chromosomes. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 27: 65-71. PMID 86582 DOI: 10.1177/27.1.86582 |
0.454 |
|
| 1978 |
Loveday KS, Latt SA. Search for DNA interchange corresponding to sister chromatid exchanges in Chinese hamster ovary cells. Nucleic Acids Research. 5: 4087-104. PMID 724509 DOI: 10.1093/Nar/5.11.4087 |
0.424 |
|
| 1978 |
Munroe SH, Latt SA. Comparison of the subunit organization of early and late replicating chromatin. Experimental Cell Research. 110: 299-313. PMID 590358 DOI: 10.1016/0014-4827(77)90296-8 |
0.432 |
|
| 1978 |
Latt SA, Schreck RR, Loveday KS, Shuler CF. In vitro and in vivo analysis of sister chromatid exchange Pharmacological Reviews. 30: 501-535. PMID 392544 |
0.354 |
|
| 1978 |
Allen JW, Shuler CF, Latt SA. Bromodeoxyuridine tablet methodology for in vivo - Studies of DNA synthesis Somatic Cell Genetics. 4: 393-405. PMID 356290 DOI: 10.1007/Bf01538862 |
0.469 |
|
| 1978 |
de la Chapelle A, Grönman P, Latt SA. Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosome. Cytogenetics and Cell Genetics. 20: 204-12. PMID 348409 DOI: 10.1159/000130852 |
0.358 |
|
| 1978 |
Latt SA. Analysis of sister chromatid exchange and chromosome replication kinetics using Brd-U-dye techniques. Virchows Archiv. B, Cell Pathology. 29: 19-27. PMID 83051 DOI: 10.1007/Bf02899332 |
0.493 |
|
| 1978 |
Sahar E, Latt SA. Enhancement of banding patterns in human metaphase chromosomes by energy transfer. Proceedings of the National Academy of Sciences of the United States of America. 75: 5650-4. PMID 82970 DOI: 10.1073/Pnas.75.11.5650 |
0.435 |
|
| 1978 |
Latt SA. Fluorescent probes of chromosome structure and replication. Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie. 19: 603-23. PMID 76502 DOI: 10.1139/G77-065 |
0.407 |
|
| 1978 |
Schwartz AL, Cole FS, Fiedorek F, Matthews D, Frantz ID, Paika I, Latt SA. 1022 PHOTOTHERAPY DOES NOT INCREASE THE SISTER CHROMATID EXCHANGE FREQUENCY IN PREMATURE INFANTS Pediatric Research. 12: 534-534. DOI: 10.1203/00006450-197804001-01028 |
0.317 |
|
| 1978 |
McCAW BK, Latt SA. X-Chromosome Replication In Parthfnogenic Benign Ovarian Teratomas Obstetrical & Gynecological Survey. 33: 607-608. DOI: 10.1097/00006254-197809000-00018 |
0.457 |
|
| 1977 |
Allen JW, Shuler CF, Mendes RW, Latt SA. A simplified technique for in vivo analysis of sister-chromatid exchanges using 5-bromodeoxyuridine tablets. Cytogenetics and Cell Genetics. 18: 231-7. PMID 872628 DOI: 10.1159/000130765 |
0.341 |
|
| 1977 |
Latt SA, George YS, Gray JW. Flow cytometric analysis of bromodeoxyuridine substituted cells stained with 33258 Hoechst Journal of Histochemistry and Cytochemistry. 25: 927-934. PMID 70460 DOI: 10.1177/25.7.70460 |
0.33 |
|
| 1977 |
Zack GW, Rogers WE, Latt SA. Automatic measurement of sister chromatid exchange frequency. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 25: 741-53. PMID 70454 DOI: 10.1177/25.7.70454 |
0.337 |
|
| 1977 |
Latt SA. Fluorescence analysis of late DNA replication in human metaphase chromosomes. Somatic Cell Genetics. 1: 293-321. PMID 68549 DOI: 10.1007/Bf01538452 |
0.529 |
|
| 1976 |
Allen JW, Latt SA. Analysis of sister chromatid exchange formation in vivo in mouse spermatogonia as a new test system for environmental mutagens Nature. 260: 449-451. PMID 1256591 DOI: 10.1038/260449A0 |
0.446 |
|
| 1976 |
Zack GW, Spriet JA, Latt SA, Granlund GH, Young IT. Automatic detection and localization of sister chromatid exchanges. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 24: 168-77. PMID 1254915 DOI: 10.1177/24.1.1254915 |
0.308 |
|
| 1976 |
Latt SA, Wohlleb JC. Optical studies of the interaction of 33258 Hoechst with DNA, chromatin, and metaphase chromosomes. Chromosoma. 52: 297-316. PMID 1192901 DOI: 10.1007/Bf00364015 |
0.429 |
|
| 1976 |
Latt SA, Stetten G, Juergens LA, Buchanan GR, Gerald PS. Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. Proceedings of the National Academy of Sciences of the United States of America. 72: 4066-70. PMID 1060089 DOI: 10.1073/Pnas.72.10.4066 |
0.422 |
|
| 1976 |
Latt SA, Willard HF, Gerald PS. BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes. Chromosoma. 57: 135-53. PMID 954550 DOI: 10.1007/Bf00292912 |
0.49 |
|
| 1976 |
Latt SA, Stetten G. Spectral studies on 33258 Hoechst and related bisbenzimidazole dyes useful for fluorescent detection of deoxyribonucleic acid synthesis. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 24: 24-33. PMID 943439 DOI: 10.1177/24.1.943439 |
0.424 |
|
| 1976 |
Stetten G, Latt SA, Davidson RL. 33258 Hoechst enhancement of the photosensitivity of bromodeoxyuridine-substituted cells. Somatic Cell Genetics. 2: 285-90. PMID 69327 DOI: 10.1007/Bf01538967 |
0.316 |
|
| 1976 |
Allen JW, Latt SA. In vivo BrdU-33258 Hoechst analysis of DNA replication kinetics and sister chromatid exchange formation in mouse somatic and meiotic cells Chromosoma. 58: 325-340. PMID 63363 DOI: 10.1007/Bf00292841 |
0.513 |
|
| 1976 |
Madan K, Allen JW, Gerald PS, Latt SA. Fluorescence analysis of late DNA replication in mouse metaphase chromosomes using BUdR and 33258 Hoechst. Experimental Cell Research. 99: 438-44. PMID 57878 DOI: 10.1016/0014-4827(76)90604-2 |
0.546 |
|
| 1975 |
Latt SA, Brodie S, Munroe SH. Optical studies of complexes of quinacrine with DNA and chromatin: implications for the fluorescence of cytological chromosome preparations. Chromosoma. 49: 17-40. PMID 4614958 DOI: 10.1007/Bf00284985 |
0.484 |
|
| 1975 |
Latt SA. Detection of DNA synthesis in interphase nuclei by fluorescence microscopy. The Journal of Cell Biology. 62: 546-50. PMID 4139167 DOI: 10.1083/Jcb.62.2.546 |
0.38 |
|
| 1975 |
Latt SA, Stetten G, Juergens LA, Willard HF, Scher CD. Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 23: 493-505. PMID 1095650 DOI: 10.1177/23.7.1095650 |
0.431 |
|
| 1974 |
Latt SA. Microfluorometric analysis of DNA replication in human X chromosomes. Experimental Cell Research. 86: 412-5. PMID 4842351 DOI: 10.1016/0014-4827(74)90733-2 |
0.549 |
|
| 1974 |
Lin MS, Latt SA, Davidson RL. Microfluorometric detection of asymmetry in the centromeric region of mouse chromosomes. Experimental Cell Research. 86: 392-5. PMID 4842349 DOI: 10.1016/0014-4827(74)90727-7 |
0.504 |
|
| 1974 |
Latt SA. Sister chromatid exchanges, indices of human chromosome damage and repair: detection by fluorescence and induction by mitomycin C. Proceedings of the National Academy of Sciences of the United States of America. 71: 3162-6. PMID 4137928 DOI: 10.1073/Pnas.71.8.3162 |
0.512 |
|
| 1974 |
Latt SA, Davidson RL, Lin MS, Gerald PS. Lateral asymmetry in the fluorescence of human Y chromosomes stained with 33 258 Hoechst. Experimental Cell Research. 87: 425-9. PMID 4137743 DOI: 10.1016/0014-4827(74)90510-2 |
0.508 |
|
| 1974 |
Lin MS, Latt SA, Davidson RL. Identification of human and mouse chromosomes in human-mouse hybrids by centromere fluorescence. Experimental Cell Research. 87: 429-33. PMID 4137714 DOI: 10.1016/0014-4827(74)90511-4 |
0.466 |
|
| 1974 |
Latt SA. Microfluorometric analysis of deoxyribonucleic acid replication kinetics and sister chromatid exchanges in human chromosomes. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 22: 478-91. PMID 4137061 DOI: 10.1177/22.7.478 |
0.56 |
|
| 1974 |
Latt SA. Localization of sister chromatid exchanges in human chromosomes. Science (New York, N.Y.). 185: 74-6. PMID 4134970 DOI: 10.1126/Science.185.4145.74 |
0.491 |
|
| 1974 |
Latt SA. Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 70: 3395-9. PMID 4128545 DOI: 10.1073/Pnas.70.12.3395 |
0.572 |
|
| 1974 |
Latt SA, Gerald PS. Staining of human metaphase chromosomes with fluorescent conjugates of polylysine. Experimental Cell Research. 81: 401-6. PMID 4128136 DOI: 10.1016/0014-4827(73)90529-6 |
0.464 |
|
| 1974 |
Latt SA, Gerald PS. MICROFLUOROMETRIC ANALYSIS OF SISTER CHROMATID EXCHANGES, INDICES OF CHROMOSOME FRAGILITY Pediatric Research. 8: 391-391. DOI: 10.1203/00006450-197404000-00304 |
0.373 |
|
| 1972 |
Latt SA, Auld DS, Vallee BL. Fluorescence determination of carboxypeptidase A activity based on electronic energy transfer Analytical Biochemistry. 50: 56-62. PMID 5080737 DOI: 10.1016/0003-2697(72)90485-X |
0.443 |
|
| 1972 |
Latt SA, Auld DS, Vallee BL. Distance measurements at the active site of carboxypeptidase A during catalysis Biochemistry. 11: 3015-3022. PMID 5041907 DOI: 10.1021/Bi00766A013 |
0.406 |
|
| 1972 |
Auld DS, Latt SA, Vallee BL. An Approach to inhibition kinetics. Measurement of enzyme-substrate complexes by electronic energy transfer Biochemistry. 11: 4994-4999. PMID 4674074 DOI: 10.1021/Bi00776A019 |
0.408 |
|
| 1972 |
Vallee BL, Riordan JF, Auld DS, Latt SA. Chemical approaches to the mode of action of carboxypeptidase A. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 257: 215-30. PMID 4399046 DOI: 10.1098/Rstb.1970.0021 |
0.439 |
|
| 1969 |
Latt SA, Holmquist B, Vallee BL. Thermolysin: A zinc metalloenzyme Biochemical and Biophysical Research Communications. 37: 333-339. PMID 5823940 DOI: 10.1016/0006-291X(69)90739-6 |
0.416 |
|
| 1967 |
Latt SA, Sober HA. Protein-nucleic acid interactions. II. Oligopeptide-polyribonucleotide binding studies. Biochemistry. 6: 3293-306. PMID 6056990 DOI: 10.1021/Bi00862A040 |
0.526 |
|
| 1967 |
Latt SA, Sober HA. Protein-nucleic acid interactions. 3. Cation effect on binding strength and specificity. Biochemistry. 6: 3307-14. PMID 4861938 DOI: 10.1021/Bi00862A041 |
0.531 |
|
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