Fred D. Ledley, M.D. - Publications

1983-1995 Cell Biology Baylor College of Medicine, Houston, TX 
 2005- Natural & Applied Science, Management, Center for Integration of Science and Industry Bentley University 
genetic medicine, personalized medicine, biotechnology, drug development, management

15 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
1993 O'Malley BW, Finegold MJ, Ledley FD. Autologous, orthotopic thyroid follicular cell transplantation: a surgical component of ex vivo somatic gene therapy. Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery. 108: 51-62. PMID 8437874 DOI: 10.1177/019459989310800107  0.32
1993 Soriano HE, Gest AL, Bair DK, Vander Straten M, Lewis DE, Darlington GJ, Finegold MJ, Ledley FD. Feasibility of hepatocellular transplantation via the umbilical vein in prenatal and perinatal lambs. Fetal Diagnosis and Therapy. 8: 293-304. PMID 8267863 DOI: 10.1159/000263843  0.36
1992 Ledley FD, Soriano HE, O'Malley BW, Lewis D, Darlington GJ, Finegold M. DiI as a marker for cellular transplantation into solid organs. Biotechniques. 13: 580, 582, 584-7. PMID 1282342  0.36
1990 Ledley FD, Grenett HE, Dunbar BS, Woo SL. Mouse phenylalanine hydroxylase. Homology and divergence from human phenylalanine hydroxylase. The Biochemical Journal. 267: 399-405. PMID 2334400 DOI: 10.1042/Bj2670399  0.48
1988 Ledley FD, Ledbetter SA, Ledbetter DH, Woo SL. Localization of mouse phenylalanine hydroxylase locus on chromosome 10. Cytogenetics and Cell Genetics. 47: 125-6. PMID 3378451 DOI: 10.1159/000132528  0.48
1987 Marvit J, DiLella AG, Brayton K, Ledley FD, Robson KJ, Woo SL. GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuria. Nucleic Acids Research. 15: 5613-28. PMID 3615198 DOI: 10.1093/Nar/15.14.5613  0.32
1987 Ledley FD, Woo SL. P-chlorophenylalanine does not inhibit production of recombinant human phenylalanine hydroxylase in NIH3T3 cells or E. coli. Biochemical and Biophysical Research Communications. 142: 302-8. PMID 2949745 DOI: 10.1016/0006-291X(87)90273-7  0.68
1987 Woo SL, DiLella AG, Marvit J, Ledley FD. Molecular basis of phenylketonuria and potential somatic gene therapy. Cold Spring Harbor Symposia On Quantitative Biology. 395-401. PMID 2884065 DOI: 10.1101/Sqb.1986.051.01.047  0.72
1987 Ledley FD, Darlington G, Hahn T, Woo SLC, Beaudet A. Gene Transfer Into Primary Hepatocytes For Somatic Gene Therapy Pediatric Research. 21: 291-291. DOI: 10.1203/00006450-198704010-00745  0.36
1986 Ledley FD, Levy HL, Woo SL. Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disorders. The New England Journal of Medicine. 314: 1276-80. PMID 3702929 DOI: 10.1056/Nejm198605153142002  0.56
1986 Ledley FD, Grenett HE, McGinnis-Shelnutt M, Woo SL. Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cells. Proceedings of the National Academy of Sciences of the United States of America. 83: 409-13. PMID 3455778 DOI: 10.1073/Pnas.83.2.409  0.76
1985 Ledley FD, Levy HL, Lidsky AS, Woo SLC. 1225 Pku And Mild Hyperphenylalaninemia (Mhp) In Siblings: Biochemical Characterization And Molecular Rflp Analysis Of The Phenylalanine Hydroxylase (Pah) Gene Pediatric Research. 19: 315-315. DOI: 10.1203/00006450-198504000-01255  0.72
1985 Ledley FD, DiLella AG, Woo SLC. Molecular biology of phenylalanine hydroxylase and phenylketonuria Trends in Genetics. 1: 309-313. DOI: 10.1016/0168-9525(85)90121-0  0.72
1984 Wang JY, Ledley F, Goff S, Lee R, Groner Y, Baltimore D. The mouse c-abl locus: molecular cloning and characterization. Cell. 36: 349-56. PMID 6319018 DOI: 10.1016/0092-8674(84)90228-9  0.4
1983 Ledley FD. Book ReviewThe Growth of Biological Thought: Diversity, evolution and inheritance New England Journal of Medicine. 308: 1174-1175. DOI: 10.1056/NEJM198305123081929  0.32
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