C. Thomas Caskey - Publications

Baylor College of Medicine, Houston, TX 
medical genetics

91 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.303
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  0.527
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  0.369
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  0.308
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  0.312
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  0.308
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  0.327
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  0.391
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  0.351
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  0.323
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  0.37
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  0.336
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  0.569
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  0.428
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  0.319
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  0.338
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  0.504
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  0.471
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  0.377
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  0.41
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  0.393
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  0.45
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  0.373
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  0.352
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  0.398
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  0.439
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  0.312
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  0.376
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  0.358
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  0.361
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  0.412
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  0.572
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  0.377
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  0.521
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  0.476
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  0.385
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  0.363
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  0.394
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  0.534
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  0.365
1989 Nelson DL, Ledbetter SA, Corbo L, Victoria MF, Ramírez-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  0.38
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  0.455
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  0.546
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  0.338
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  0.343
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  0.561
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  0.517
1985 Patel PI, Caskey CT. HPRT and the Lesch?Nyhan syndrome Bioessays. 2: 4-8. DOI: 10.1002/BIES.950020103  0.441
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  0.572
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  0.562
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  0.459
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  0.435
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  0.361
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  0.378
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  0.348
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
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