| Year |
Citation |
Score |
| 2020 |
Hou YC, Yu HC, Martin R, Cirulli ET, Schenker-Ahmed NM, Hicks M, Cohen IV, Jönsson TJ, Heister R, Napier L, Swisher CL, Dominguez S, Tang H, Li W, Perkins BA, ... ... Caskey CT, et al. Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging. Proceedings of the National Academy of Sciences of the United States of America. PMID 31980526 DOI: 10.1073/Pnas.1909378117 |
0.31 |
|
| 2018 |
Shah N, Hou YC, Yu HC, Sainger R, Caskey CT, Venter JC, Telenti A. Identification of Misclassified ClinVar Variants via Disease Population Prevalence. American Journal of Human Genetics. 102: 609-619. PMID 29625023 DOI: 10.1016/J.Ajhg.2018.02.019 |
0.302 |
|
| 2017 |
Tang H, Kirkness EF, Lippert C, Biggs WH, Fabani M, Guzman E, Ramakrishnan S, Lavrenko V, Kakaradov B, Hou C, Hicks B, Heckerman D, Och FJ, Caskey CT, Venter JC, et al. Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes. American Journal of Human Genetics. 101: 700-715. PMID 29100084 DOI: 10.1016/J.Ajhg.2017.09.013 |
0.32 |
|
| 2017 |
Long T, Hicks M, Yu HC, Biggs WH, Kirkness EF, Menni C, Zierer J, Small KS, Mangino M, Messier H, Brewerton S, Turpaz Y, Perkins BA, Evans AM, Miller LA, ... ... Caskey CT, et al. Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites. Nature Genetics. PMID 28263315 DOI: 10.1038/Ng.3809 |
0.309 |
|
| 2015 |
Guo L, Milburn MV, Ryals JA, Lonergan SC, Mitchell MW, Wulff JE, Alexander DC, Evans AM, Bridgewater B, Miller L, Gonzalez-Garay ML, Caskey CT. Plasma metabolomic profiles enhance precision medicine for volunteers of normal health. Proceedings of the National Academy of Sciences of the United States of America. 112: E4901-10. PMID 26283345 DOI: 10.1073/pnas.1508425112 |
0.308 |
|
| 2014 |
Caskey CT, Leder P. The RNA code: nature's Rosetta Stone. Proceedings of the National Academy of Sciences of the United States of America. 111: 5758-9. PMID 24756939 DOI: 10.1073/pnas.1404819111 |
0.498 |
|
| 2014 |
Brownstein CA, Beggs AH, Homer N, Merriman B, Yu TW, Flannery KC, DeChene ET, Towne MC, Savage SK, Price EN, Holm IA, Luquette LJ, Lyon E, Majzoub J, Neupert P, ... ... Caskey CT, et al. An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. Genome Biology. 15: R53. PMID 24667040 DOI: 10.1186/Gb-2014-15-3-R53 |
0.302 |
|
| 2013 |
Gonzalez-Garay ML, McGuire AL, Pereira S, Caskey CT. Personalized genomic disease risk of volunteers. Proceedings of the National Academy of Sciences of the United States of America. 110: 16957-62. PMID 24082139 DOI: 10.1073/pnas.1315934110 |
0.332 |
|
| 2013 |
Schaaf CP, Gonzalez-Garay ML, Xia F, Potocki L, Gripp KW, Zhang B, Peters BA, McElwain MA, Drmanac R, Beaudet AL, Caskey CT, Yang Y. Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. Nature Genetics. 45: 1405-8. PMID 24076603 DOI: 10.1038/Ng.2776 |
0.526 |
|
| 2005 |
Ohbayashi F, Balamotis MA, Kishimoto A, Aizawa E, Diaz A, Hasty P, Graham FL, Caskey CT, Mitani K. Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors. Proceedings of the National Academy of Sciences of the United States of America. 102: 13628-33. PMID 16174752 DOI: 10.1073/Pnas.0506598102 |
0.368 |
|
| 2000 |
Sandig V, Youil R, Bett AJ, Franlin LL, Oshima M, Maione D, Wang F, Metzker ML, Savino R, Caskey CT. Optimization of the helper-dependent adenovirus system for production and potency in vivo. Proceedings of the National Academy of Sciences of the United States of America. 97: 1002-7. PMID 10655474 DOI: 10.1073/pnas.97.3.1002 |
0.307 |
|
| 1999 |
Gerhold D, Rushmore T, Caskey CT. DNA chips: promising toys have become powerful tools. Trends in Biochemical Sciences. 24: 168-73. PMID 10322428 DOI: 10.1016/S0968-0004(99)01382-1 |
0.315 |
|
| 1999 |
Chen F, Zhang Q, McDonald T, Davidoff MJ, Bailey W, Bai C, Liu Q, Caskey CT. Identification of two hERR2-related novel nuclear receptors utilizing bioinformatics and inverse PCR. Gene. 228: 101-9. PMID 10072763 DOI: 10.1016/S0378-1119(98)00619-2 |
0.363 |
|
| 1998 |
Harvey DM, Caskey CT. Inducible control of gene expression: prospects for gene therapy. Current Opinion in Chemical Biology. 2: 512-8. PMID 9736925 DOI: 10.1016/S1367-5931(98)80128-2 |
0.311 |
|
| 1998 |
Brown SD, Twells RC, Hey PJ, Cox RD, Levy ER, Soderman AR, Metzker ML, Caskey CT, Todd JA, Hess JF. Isolation and characterization of LRP6, a novel member of the low density lipoprotein receptor gene family. Biochemical and Biophysical Research Communications. 248: 879-88. PMID 9704021 DOI: 10.1006/Bbrc.1998.9061 |
0.307 |
|
| 1998 |
McDonald T, Wang R, Bailey W, Xie G, Chen F, Caskey CT, Liu Q. Identification and cloning of an orphan G protein-coupled receptor of the glycoprotein hormone receptor subfamily. Biochemical and Biophysical Research Communications. 247: 266-70. PMID 9642114 DOI: 10.1006/bbrc.1998.8774 |
0.326 |
|
| 1996 |
Gerhold D, Caskey CT. It's the genes! EST access to human genome content. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 18: 973-81. PMID 8976154 DOI: 10.1002/bies.950181207 |
0.39 |
|
| 1996 |
Timchenko LT, Miller JW, Timchenko NA, DeVore DR, Datar KV, Lin L, Roberts R, Caskey CT, Swanson MS. Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy. Nucleic Acids Research. 24: 4407-14. PMID 8948631 DOI: 10.1093/nar/24.22.4407 |
0.3 |
|
| 1996 |
DeMarchi JM, Caskey CT, Richards CS. Population-specific screening by mutation analysis for diseases frequent in Ashkenazi Jews. Human Mutation. 8: 116-25. PMID 8844209 DOI: 10.1002/(SICI)1098-1004(1996)8:2<116::AID-HUMU3>3.0.CO;2-9 |
0.306 |
|
| 1996 |
Ashizawa T, Monckton DG, Vaishnav S, Patel BJ, Voskova A, Caskey CT. Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy. Genomics. 36: 47-53. PMID 8812415 DOI: 10.1006/Geno.1996.0424 |
0.35 |
|
| 1996 |
Shumaker JM, Metspalu A, Caskey CT. Mutation detection by solid phase primer extension. Human Mutation. 7: 346-54. PMID 8723685 DOI: 10.1002/(SICI)1098-1004(1996)7:4<346::AID-HUMU9>3.0.CO;2-6 |
0.322 |
|
| 1996 |
Zhao Z, Lee CC, Monckton DG, Yazdani A, Coolbaugh MI, Li X, Bailey J, Shen Y, Caskey CT. Characterization and genomic mapping of genes and pseudogenes of a new human protein tyrosine phosphatase. Genomics. 35: 172-81. PMID 8661118 DOI: 10.1006/geno.1996.0336 |
0.369 |
|
| 1995 |
Clemens PR, Krause TL, Chan S, Korb KE, Graham FL, Caskey CT. Recombinant truncated dystrophin minigenes: construction, expression, and adenoviral delivery. Human Gene Therapy. 6: 1477-85. PMID 8573620 DOI: 10.1089/Hum.1995.6.11-1477 |
0.335 |
|
| 1995 |
Mitani K, Wakamiya M, Hasty P, Graham FL, Bradley A, Caskey CT. Gene targeting in mouse embryonic stem cells with an adenoviral vector. Somatic Cell and Molecular Genetics. 21: 221-31. PMID 8525428 DOI: 10.1007/Bf02255777 |
0.321 |
|
| 1995 |
Panzer S, Kuhl DP, Caskey CT. Unstable triplet repeat sequences: a source of cancer mutations? Stem Cells (Dayton, Ohio). 13: 146-57. PMID 7787780 DOI: 10.1002/stem.5530130206 |
0.365 |
|
| 1995 |
Zhao Z, Lee CC, Jiralerspong S, Juyal RC, Lu F, Baldini A, Greenberg F, Caskey CT, Patel PI. The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients. Human Molecular Genetics. 4: 589-97. PMID 7633408 DOI: 10.1093/Hmg/4.4.589 |
0.563 |
|
| 1995 |
Zhao Z, Lee CC, Baldini A, Caskey CT. A human homologue of the Drosophila polarity gene frizzled has been identified and mapped to 17q21.1. Genomics. 27: 370-3. PMID 7558010 DOI: 10.1006/geno.1995.1060 |
0.364 |
|
| 1994 |
DeMarchi JM, Beaudet AL, Caskey CT, Richards CS. Experience of an academic reference laboratory using automation for analysis of cystic fibrosis mutations. Archives of Pathology & Laboratory Medicine. 118: 26-32. PMID 8285831 |
0.427 |
|
| 1994 |
Faustinella F, Kwon H, Serrano F, Belmont JW, Caskey CT, Aguilar-Cordova E. A new family of murine retroviral vectors with extended multiple cloning sites for gene insertion. Human Gene Therapy. 5: 307-12. PMID 8018745 DOI: 10.1089/hum.1994.5.3-307 |
0.328 |
|
| 1994 |
Mitani K, Graham FL, Caskey CT. Transduction of human bone marrow by adenoviral vector. Human Gene Therapy. 5: 941-8. PMID 7948143 DOI: 10.1089/hum.1994.5.8-941 |
0.318 |
|
| 1994 |
Puers C, Hammond HA, Caskey CT, Lins AM, Sprecher CJ, Brinkmann B, Schumm JW. Allelic ladder characterization of the short tandem repeat polymorphism located in the 5' flanking region to the human coagulation factor XIII A subunit gene. Genomics. 23: 260-4. PMID 7829085 DOI: 10.1006/geno.1994.1490 |
0.337 |
|
| 1993 |
Perryman MB, Friedman DL, Fu YH, Caskey CT. Molecular genetics of myotonic dystrophy. Trends in Cardiovascular Medicine. 3: 82-4. PMID 21244944 DOI: 10.1016/1050-1738(93)90028-5 |
0.503 |
|
| 1993 |
Redman JB, Fenwick RG, Fu YH, Pizzuti A, Caskey CT. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring. Jama. 269: 1960-5. PMID 8464127 DOI: 10.1001/jama.1993.03500150072029 |
0.469 |
|
| 1993 |
Reiner O, Carrozzo R, Shen Y, Wehnert M, Faustinella F, Dobyns WB, Caskey CT, Ledbetter DH. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Nature. 364: 717-21. PMID 8355785 DOI: 10.1038/364717A0 |
0.364 |
|
| 1993 |
Kuhl DP, Caskey CT. Trinucleotide repeats and genome variation. Current Opinion in Genetics & Development. 3: 404-7. PMID 8353413 DOI: 10.1016/0959-437X(93)90112-3 |
0.331 |
|
| 1993 |
Morsy MA, Mitani K, Clemens P, Caskey CT. Progress toward human gene therapy. Jama. 270: 2338-45. PMID 8230597 DOI: 10.1001/Jama.1993.03510190094033 |
0.344 |
|
| 1993 |
Wang Q, Ishikawa-Brush Y, Monaco AP, Nelson DL, Caskey CT, Pauly SP, Lenoir GM, Sylla BS. Physical mapping of Xq24-25 around loci closely linked to the X-linked lymphoproliferative syndrome locus: an overlapping YAC map and linkage between DXS12, DXS42, and DXS37. European Journal of Human Genetics : Ejhg. 1: 64-71. PMID 8069652 DOI: 10.1159/000472388 |
0.375 |
|
| 1993 |
Zu Z, Yu Y, Gibbs RA, Caskey CT, Hsie AW. Multiplex DNA amplification and solid-phase direct sequencing for mutation analysis at the hprt locus in Chinese hamster cells. Mutation Research. 288: 237-48. PMID 7688083 DOI: 10.1016/0027-5107(93)90090-3 |
0.368 |
|
| 1992 |
Riggins GJ, Sherman SL, Oostra BA, Sutcliffe JS, Feitell D, Nelson DL, Van Oost BA, Smits APT, Ramos FJ, Pfendner E, Kuhl DPA, Caskey CT, Warren ST. Characterization of a highly polymorphic dinucleotide repeat 150 kb proximal to the fragile X site American Journal of Medical Genetics. 43: 237-243. PMID 1605197 DOI: 10.1002/Ajmg.1320430138 |
0.407 |
|
| 1992 |
Kilimann MW, Pizzuti A, Grompe M, Caskey CT. Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR. Human Genetics. 89: 253-8. PMID 1601417 DOI: 10.1007/BF00220535 |
0.392 |
|
| 1992 |
Caskey CT, Pizzuti A, Fu YH, Fenwick RG, Nelson DL. Triplet repeat mutations in human disease. Science (New York, N.Y.). 256: 784-9. PMID 1589758 DOI: 10.1126/Science.1589758 |
0.449 |
|
| 1992 |
Grompe M, Pieretti M, Caskey CT, Ballabio A. The sulfatase gene family: cross-species PCR cloning using the MOPAC technique. Genomics. 12: 755-60. PMID 1572648 DOI: 10.1016/0888-7543(92)90306-D |
0.372 |
|
| 1992 |
Grompe M, Jones SN, Loulseged H, Caskey CT. Retroviral-mediated gene transfer of human ornithine transcarbamylase into primary hepatocytes of spf and spf-ash mice. Human Gene Therapy. 3: 35-44. PMID 1562638 DOI: 10.1089/hum.1992.3.1-35 |
0.331 |
|
| 1992 |
Wu XW, Muzny DM, Lee CC, Caskey CT. Two independent mutational events in the loss of urate oxidase during hominoid evolution. Journal of Molecular Evolution. 34: 78-84. PMID 1556746 DOI: 10.1007/Bf00163854 |
0.351 |
|
| 1992 |
Ashizawa T, Dubel JR, Dunne PW, Dunne CJ, Fu YH, Pizzuti A, Caskey CT, Boerwinkle E, Perryman MB, Epstein HF. Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat. Neurology. 42: 1877-83. PMID 1407566 DOI: 10.1212/Wnl.42.10.1877 |
0.396 |
|
| 1992 |
Cohen-Haguenauer O, Caskey CT, Boiron M. First International Workshop on Human Gene Transfer. Human Gene Therapy. 3: 163-5. PMID 1391036 DOI: 10.1089/hum.1992.3.2-163 |
0.302 |
|
| 1992 |
Sutcliffe JS, Zhang F, Caskey CT, Nelson DL, Warren ST. PCR amplification and analysis of yeast artificial chromosomes. Genomics. 13: 1303-6. PMID 1380485 DOI: 10.1016/0888-7543(92)90051-S |
0.436 |
|
| 1992 |
Caskey CT. Antisense and differentiation. Annals of the New York Academy of Sciences. 660: 154-8. PMID 1340118 DOI: 10.1111/j.1749-6632.1992.tb21067.x |
0.311 |
|
| 1992 |
Pizzuti A, Pieretti M, Fenwick RG, Gibbs RA, Caskey CT. A transposon-like element in the deletion-prone region of the dystrophin gene. Genomics. 13: 594-600. PMID 1322353 DOI: 10.1016/0888-7543(92)90129-G |
0.375 |
|
| 1992 |
Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST. DNA methylation represses FMR-1 transcription in fragile X syndrome. Human Molecular Genetics. 1: 397-400. PMID 1301913 DOI: 10.1093/hmg/1.6.397 |
0.355 |
|
| 1991 |
Nelson DL, Ballabio A, Victoria MF, Pieretti M, Bies RD, Gibbs RA, Maley JA, Chinault AC, Webster TD, Caskey CT. Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus. Proceedings of the National Academy of Sciences of the United States of America. 88: 6157-61. PMID 2068096 DOI: 10.1073/Pnas.88.14.6157 |
0.357 |
|
| 1991 |
Rossiter BJ, Fuscoe JC, Muzny DM, Fox M, Caskey CT. The Chinese hamster HPRT gene: restriction map, sequence analysis, and multiplex PCR deletion screen. Genomics. 9: 247-56. PMID 2004774 DOI: 10.1016/0888-7543(91)90249-E |
0.411 |
|
| 1991 |
Pieretti M, Zhang FP, Fu YH, Warren ST, Oostra BA, Caskey CT, Nelson DL. Absence of expression of the FMR-1 gene in fragile X syndrome. Cell. 66: 817-22. PMID 1878973 DOI: 10.1016/0092-8674(91)90125-I |
0.57 |
|
| 1991 |
Gordon RB, Dawson PA, Sculley DG, Emmerson BT, Caskey CT, Gibbs RA. The molecular characterisation of HPRT CHERMSIDE and HPRT COORPAROO: two Lesch-Nyhan patients with reduced amounts of mRNA. Gene. 108: 299-304. PMID 1840549 DOI: 10.1016/0378-1119(91)90450-P |
0.376 |
|
| 1991 |
Lee CC, Pearlman JA, Chamberlain JS, Caskey CT. Expression of recombinant dystrophin and its localization to the cell membrane. Nature. 349: 334-6. PMID 1824797 DOI: 10.1038/349334a0 |
0.52 |
|
| 1991 |
Cournoyer D, Scarpa M, Mitani K, Moore KA, Markowitz D, Bank A, Belmont JW, Caskey CT. Gene transfer of adenosine deaminase into primitive human hematopoietic progenitor cells. Human Gene Therapy. 2: 203-13. PMID 1751590 DOI: 10.1089/Hum.1991.2.3-203 |
0.319 |
|
| 1991 |
Blonden LAJ, Grootscholten PM, den Dunnen JT, Bakker E, Abbs S, Bobrow M, Boehm C, van Broeckhoven C, Baumbach L, Chamberlain J, Caskey CT, Denton M, Felicetti L, Galluzi G, Fischbeck KH, et al. 242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread Genomics. 10: 631-639. PMID 1679746 DOI: 10.1016/0888-7543(91)90445-K |
0.474 |
|
| 1990 |
Cook-Deegan RM, Guyer M, Rossiter BJ, Nelson DL, Caskey CT. The large DNA insert cloning workshop. Genomics. 7: 654-60. PMID 2387593 DOI: 10.1016/0888-7543(90)90215-G |
0.382 |
|
| 1990 |
Cook-Deegan RM, Rossiter BJ, Engel L, Nelson DL, Caskey CT. Report of the X chromosome workshop. Genomics. 7: 647-54. PMID 2387592 DOI: 10.1016/0888-7543(90)90214-F |
0.36 |
|
| 1990 |
Corbo L, Maley JA, Nelson DL, Caskey CT. Direct cloning of human transcripts with HnRNA from hybrid cell lines. Science (New York, N.Y.). 249: 652-5. PMID 2382140 DOI: 10.1126/Science.2382140 |
0.391 |
|
| 1990 |
Gibbs RA, Nguyen PN, Edwards A, Civitello AB, Caskey CT. Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families. Genomics. 7: 235-44. PMID 2347587 DOI: 10.1016/0888-7543(90)90545-6 |
0.302 |
|
| 1990 |
Edwards A, Voss H, Rice P, Civitello A, Stegemann J, Schwager C, Zimmermann J, Erfle H, Caskey CT, Ansorge W. Automated DNA sequencing of the human HPRT locus. Genomics. 6: 593-608. PMID 2341149 DOI: 10.1016/0888-7543(90)90493-E |
0.321 |
|
| 1990 |
Ballabio A, Ranier JE, Chamberlain JS, Zollo M, Caskey CT. Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification. Human Genetics. 84: 571-3. PMID 2338343 DOI: 10.1007/Bf00210812 |
0.532 |
|
| 1990 |
Caskey CT, Kaback MM, Beaudet AL. The American Society of Human Genetics statement on cystic fibrosis screening. American Journal of Human Genetics. 46: 393. PMID 2301404 |
0.364 |
|
| 1989 |
Nelson DL, Ledbetter SA, Corbo L, Victoria MF, RamÃrez-Solis R, Webster TD, Ledbetter DH, Caskey CT. Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. Proceedings of the National Academy of Sciences of the United States of America. 86: 6686-90. PMID 2771952 DOI: 10.1073/Pnas.86.17.6686 |
0.377 |
|
| 1989 |
Moore KA, Fletcher FA, Alford RL, Villalon DK, Hawkins DH, MacGregor GR, Caskey CT, Belmont JW. Expression vectors for human adenosine deaminase gene therapy. Genome / National Research Council Canada = Gã©Nome / Conseil National De Recherches Canada. 31: 832-9. PMID 2576653 DOI: 10.1139/G89-146 |
0.321 |
|
| 1988 |
Chamberlain JS, Pearlman JA, Muzny DM, Gibbs RA, Ranier JE, Caskey CT, Reeves AA. Expression of the murine Duchenne muscular dystrophy gene in muscle and brain. Science (New York, N.Y.). 239: 1416-8. PMID 3347839 DOI: 10.1126/Science.3347839 |
0.453 |
|
| 1988 |
Fletcher FA, Moore KA, MacGregor GR, Belmont JW, Caskey CT. Human gene expression in murine hemopoietic cells in vivo. Advances in Experimental Medicine and Biology. 241: 123-7. PMID 3223402 DOI: 10.1007/978-1-4684-5571-7_15 |
0.334 |
|
| 1988 |
Stout JT, Caskey CT. The Lesch-Nyhan syndrome: clinical, molecular and genetic aspects. Trends in Genetics : Tig. 4: 175-8. PMID 3076300 DOI: 10.1016/0168-9525(88)90024-8 |
0.323 |
|
| 1988 |
Yang TP, Stout JT, Konecki DS, Patel PI, Alford RL, Caskey CT. Spontaneous reversion of novel Lesch-Nyhan mutation by HPRT gene rearrangement. Somatic Cell and Molecular Genetics. 14: 293-303. PMID 2835825 |
0.541 |
|
| 1987 |
Craigen WJ, Caskey CT. Translational frameshifting: where will it stop? Cell. 50: 1-2. PMID 3297347 DOI: 10.1016/0092-8674(87)90652-0 |
0.337 |
|
| 1987 |
Craigen WJ, Caskey CT. The function, structure and regulation of E. coli peptide chain release factors. Biochimie. 69: 1031-41. PMID 3126822 DOI: 10.1016/0300-9084(87)90003-4 |
0.354 |
|
| 1986 |
Craigen WJ, Caskey CT. Expression of peptide chain release factor 2 requires high-efficiency frameshift. Nature. 322: 273-5. PMID 3736654 DOI: 10.1038/322273a0 |
0.319 |
|
| 1986 |
Nelson DL, Chang SM, Henkel-Tigges J, Wager-Smith K, Belmont JW, Caskey CT. Gene replacement therapy for inborn errors of purine metabolism. Cold Spring Harbor Symposia On Quantitative Biology. 51: 1065-71. PMID 3555977 DOI: 10.1101/SQB.1986.051.01.124 |
0.34 |
|
| 1986 |
Patel PI, Framson PE, Caskey CT, Chinault AC. Fine structure of the human hypoxanthine phosphoribosyltransferase gene. Molecular and Cellular Biology. 6: 393-403. PMID 3023844 DOI: 10.1128/Mcb.6.2.393 |
0.556 |
|
| 1986 |
Belmont JW, Henkel-Tigges J, Chang SM, Wager-Smith K, Kellems RE, Dick JE, Magli MC, Phillips RA, Bernstein A, Caskey CT. Expression of human adenosine deaminase in murine haematopoietic progenitor cells following retroviral transfer. Nature. 322: 385-7. PMID 3016551 DOI: 10.1038/322385A0 |
0.332 |
|
| 1985 |
Chang SM, Tsao TY, Patel PI, Chinault AC, Melton DW, Caskey CT. EXPRESSION OF HUMAN AND MOUSE HPRT MINIGENES: 31 Pediatric Research. 19: 749-749. DOI: 10.1203/00006450-198507000-00051 |
0.511 |
|
| 1985 |
Patel PI, Caskey CT. HPRT and the Lesch?Nyhan syndrome Bioessays. 2: 4-8. DOI: 10.1002/BIES.950020103 |
0.434 |
|
| 1984 |
Patel PI, Nussbaum RL, gramson PE, Ledbetter DH, Caskey CT, Chinault AC. Organization of the HPRT gene and related sequences in the human genome. Somatic Cell and Molecular Genetics. 10: 483-93. PMID 6089358 DOI: 10.1007/Bf01534853 |
0.568 |
|
| 1984 |
Yang TP, Patel PI, Chinault AC, Stout JT, Jackson LG, Hildebrand BM, Caskey CT. Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients. Nature. 310: 412-4. PMID 6087154 DOI: 10.1038/310412A0 |
0.557 |
|
| 1978 |
Beaudet AL, Caskey CT. Detection of Fabry's disease heterozygotes by hair root analysis. Clinical Genetics. 13: 251-8. PMID 205381 DOI: 10.1111/j.1399-0004.1978.tb01178.x |
0.458 |
|
| 1976 |
Forget BG, Hillman DG, Lazarus H, Barell EF, Benz EJ, Caskey CT, Hulsman THJ, Schroeder WA, Housman D. Absence of messenger RNA and gene DNA for β-globin chains in hereditary persistence of fetal hemoglobin Cell. 7: 323-329. PMID 947544 DOI: 10.1016/0092-8674(76)90161-6 |
0.434 |
|
| 1974 |
Caskey CT, Beaudet AL, Tate WP. Mammalian release factor; in vitro assay and purification. Methods in Enzymology. 30: 293-303. PMID 4604721 DOI: 10.1016/0076-6879(74)30032-8 |
0.36 |
|
| 1973 |
Tate WP, Beaudet AL, Caskey CT. Influence of guanine nucleotides and elongation factors on interaction of release factors with the ribosome. Proceedings of the National Academy of Sciences of the United States of America. 70: 2350-5. PMID 4525170 |
0.377 |
|
| 1972 |
Goldstein JL, Caskey CT. Peptide chain termination: effect of protein S on ribosomal binding of release factors. Proceedings of the National Academy of Sciences of the United States of America. 67: 537-43. PMID 5289007 DOI: 10.1073/PNAS.67.2.537 |
0.347 |
|
| 1972 |
Caskey CT, Beaudet AL, Scolnick EM, Rosman M. Hydrolysis of fMet-tRNA by peptidyl transferase. Proceedings of the National Academy of Sciences of the United States of America. 68: 3163-7. PMID 4943558 DOI: 10.1073/PNAS.68.12.3163 |
0.361 |
|
| 1971 |
Beaudet AL, Caskey CT. Mammalian peptide chain termination. II. Codon specificity and GTPase activity of release factor. Proceedings of the National Academy of Sciences of the United States of America. 68: 619-24. PMID 5276771 DOI: 10.1073/PNAS.68.3.619 |
0.377 |
|
| 1970 |
Goldstein JL, Beaudet AL, Caskey CT. Peptide chain termination with mammalian release factor. Proceedings of the National Academy of Sciences of the United States of America. 67: 99-106. PMID 4917818 DOI: 10.1073/PNAS.67.1.99 |
0.507 |
|
| 1968 |
Caskey CT, Beaudet A, Nirenberg M. RNA codons and protein synthesis. 15. Dissimilar responses of mammalian and bacterial transfer RNA fractions to messenger RNA codons. Journal of Molecular Biology. 37: 99-118. PMID 4939041 |
0.432 |
|
| 1968 |
Caskey CT, Tompkins R, Scolnick E, Caryk T, Nirenberg M. Sequential translation of trinucleotide codons for the initiation and termination of protein synthesis. Science (New York, N.Y.). 162: 135-8. PMID 4877370 DOI: 10.1126/Science.162.3849.135 |
0.465 |
|
| 1967 |
Marshall RE, Caskey CT, Nirenberg M. Fine structure of RNA codewords recognized by bacterial, amphibian, and mammalian transfer RNA. Science (New York, N.Y.). 155: 820-6. PMID 5335001 DOI: 10.1126/Science.155.3764.820 |
0.441 |
|
| Show low-probability matches. |
