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1دورية أكاديمية
المؤلفون: Ratnapriya, Rinki, Zhan, Xiaowei, Fariss, Robert N, Branham, Kari E, Zipprer, David, Chakarova, Christina F, Sergeev, Yuri V, Campos, Maria M, Othman, Mohammad, Friedman, James S, Maminishkis, Arvydas, Waseem, Naushin H, Brooks, Matthew, Rajasimha, Harsha K, Edwards, Albert O, Lotery, Andrew, Klein, Barbara E, Truitt, Barbara J, Li, Bingshan, Schaumberg, Debra A, Morgan, Denise J, Morrison, Margaux A, Souied, Eric, Tsironi, Evangelia E, Grassmann, Felix, Fishman, Gerald A, Silvestri, Giuliana, Scholl, Hendrik PN, Kim, Ivana K, Ramke, Jacqueline, Tuo, Jingsheng, Merriam, Joanna E, Merriam, John C, Park, Kyu Hyung, Olson, Lana M, Farrer, Lindsay A, Johnson, Matthew P, Peachey, Neal S, Lathrop, Mark, Baron, Robert V, Igo, Robert P, Klein, Ronald, Hagstrom, Stephanie A, Kamatani, Yoichiro, Martin, Tammy M, Jiang, Yingda, Conley, Yvette, Sahel, Jose-Alan, Zack, Donald J, Chan, Chi-Chao, Pericak-Vance, Margaret A, Jacobson, Samuel G, Gorin, Michael B, Klein, Michael L, Allikmets, Rando, Iyengar, Sudha K, Weber, Bernhard H, Haines, Jonathan L, Léveillard, Thierry, Deangelis, Margaret M, Stambolian, Dwight, Weeks, Daniel E, Bhattacharya, Shomi S, Chew, Emily Y, Heckenlively, John R, Abecasis, Gonçalo R, Swaroop, Anand
المصدر: Human Molecular Genetics. 23(21)
مصطلحات موضوعية: Eye Disease and Disorders of Vision, Human Genome, Neurodegenerative, Genetics, Clinical Research, Macular Degeneration, Aging, 2.1 Biological and endogenous factors, Aetiology, Eye, Adult, Aged, Amino Acid Sequence, Bruch Membrane, DNA Mutational Analysis, Exome, Extracellular Matrix, Fibrillin-2, Fibrillins, Genetic Association Studies, Genetic Variation, High-Throughput Nucleotide Sequencing, Humans, Male, Meta-Analysis as Topic, Microfilament Proteins, Middle Aged, Models, Molecular, Molecular Sequence Data, Mutation, Pedigree, Protein Conformation, Protein Stability, Retina, Sequence Alignment, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/4t34q41c
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2دورية أكاديمية
المؤلفون: Nishiguchi, Koji M., Friedman, James S., Sandberg, Michael A., Swaroop, Anand, Berson, Eliot L., Dryja, Thaddeus P.
المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2004 Dec . 101(51), 17819-17824.
URL الوصول: https://www.jstor.org/stable/3374052
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3دورية أكاديمية
المؤلفون: Friedman, James S., Chang, Bo, Krauth, Daniel S., Lopez, Irma, Waseem, Naushin H., Hurd, Ron E., Feathers, Kecia L., Branham, Kari E., Shaw, Manessa, Thomas, George E., Brooks, Matthew J., Liu, Chunqiao, Bakeri, Hirva A., Campos, Maria M., Maubaret, Cecilia, Webster, Andrew R., Rodriguez, Ignacio R., Thompson, Debra A., Bhattacharya, Shomi S., Koenekoop, Robert K., Heckenlively, John R., Swaroop, Anand, Nathans, Jeremy
المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2010 Aug . 107(35), 15523-15528.
URL الوصول: https://www.jstor.org/stable/27862283
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4دورية أكاديميةCanine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3
المؤلفون: Kukekova, Anna V., Goldstein, Orly, Johnson, Jennifer L., Richardson, Malcolm A., Pearce-Kelling, Susan E., Swaroop, Anand, Friedman, James S., Aguirre, Gustavo D., Acland, Gregory M.
المصدر: Mammalian Genome. February 2009 20(2):109-123
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5دورية أكاديمية
المؤلفون: Friedman, James S., Chang, Bo, Kannabiran, Chitra, Chakarova, Christina, Singh, Hardeep P., Jalali, Subhadra, Hawes, Norman L., Branham, Kari, Othman, Mohammad, Filippova, Elena, Thompson, Debra A., Webster, Andrew R., Andréasson, Sten, Jacobson, Samuel G., Bhattacharya, Shomi S., Heckenlively, John R., Swaroop, Anand *
المصدر: In The American Journal of Human Genetics December 2006 79(6):1059-1070
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6دورية أكاديمية
المؤلفون: Friedman, James S., Walter, Michael A.
المصدر: Molecular Biotechnology. October 2001 19(2):205-210
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7دورية أكاديمية
المؤلفون: Friedman, James S., Walter, Michael A.
المصدر: Science, 2002 Feb 01. 295(5557), 983-984.
URL الوصول: https://www.jstor.org/stable/3076079
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8
المؤلفون: Hugosson, Therése, Friedman, James S, Ponjavic, Vesna, Abrahamson, Magnus, Swaroop, Anand, Andréasson, Sten
المصدر: Archives of Ophthalmology. 128(6):772-778
مصطلحات موضوعية: Autoantigens: genetics, Retinitis Pigmentosa: genetics, Medicin och hälsovetenskap, Klinisk medicin, Oftalmologi, Medical and Health Sciences, Clinical Medicine, Ophthalmology
URL الوصول: https://lup.lub.lu.se/record/1626074
http://www.ncbi.nlm.nih.gov/pubmed/20547956?dopt=Abstract
http://dx.doi.org/10.1001/archophthalmol.2010.98 -
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المؤلفون: Friedman, James S., Ray, Joseph W., Waseem, Naushin, Johnson, Kory, Brooks, Matthew J., Hugosson, Therése, Breuer, Debra, Branham, Kari E., Krauth, Daniel S., Bowne, Sara J., Sullivan, Lori S., Ponjavic, Vesna, Gränse, Lotta, Khanna, Ritu, Trager, Edward H., Gieser, Linn M., Hughbanks-Wheaton, Dianna, Cojocaru, Radu I., Ghiasvand, Noor M., Chakarova, Christina F., Abrahamson, Magnus, Goering, Harald H. H., Webster, Andrew R., Birch, David G., Abecasis, Goncalo R., Fann, Yang, Bhattacharya, Shomi S., Daiger, Stephen P., Heckenlively, John R., Andréasson, Sten, Swaroop, Anand
المصدر: American Journal of Human Genetics. 84(6):792-800
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10دورية أكاديمية
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