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Nature Genetics
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February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
N B Haider, S G Jacobson, A V Cideciyan, et al.
Human Mutation
|
May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene
Julia Felden, Britta Baumann, Manir Ali, et al.
American Journal of Human Genetics
|
November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I
L M Astuto, M D Weston, C A Carney, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 23, 2004
Evidence that transfer of functional p53 protein results in increased apoptosis in prostate cancer
Louis L Pisters, Curtis A Pettaway, Patricia Troncoso, et al.
Nature Genetics
|
May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
K Mykytyn, T Braun, R Carmi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 18, 2004
Phase I trial of preoperative doxorubicin-based concurrent chemoradiation and surgical resection for localized extremity and body wall soft tissue sarcomas
Peter W T Pisters, Shreyaskumar R Patel, Victor G Prieto, et al.
Annals of Epidemiology
|
December 15, 2021
The Millennium Cohort Study: The first 20 years of research dedicated to understanding the long-term health of US Service Members and Veterans
Jennifer N Belding, Sheila F Castañeda, Isabel G Jacobson, et al.
American Journal of Human Genetics
|
February 18, 2004
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease
Gonçalo R Abecasis, Beverly M Yashar, Yu Zhao, et al.
Human Molecular Genetics
|
April 4, 2017
REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival
Shobi Veleri, Jacob Nellissery, Bibhudatta Mishra, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 24, 2008
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
Artur V Cideciyan, Tomas S Aleman, Sanford L Boye, et al.
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of 68
Search research articles
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Showing results (631-640 of 677) with videos related to
Sort By:
Page
of 68
Nature Genetics
|
February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
N B Haider, S G Jacobson, A V Cideciyan, et al.
Human Mutation
|
May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene
Julia Felden, Britta Baumann, Manir Ali, et al.
American Journal of Human Genetics
|
November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I
L M Astuto, M D Weston, C A Carney, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 23, 2004
Evidence that transfer of functional p53 protein results in increased apoptosis in prostate cancer
Louis L Pisters, Curtis A Pettaway, Patricia Troncoso, et al.
Nature Genetics
|
May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
K Mykytyn, T Braun, R Carmi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 18, 2004
Phase I trial of preoperative doxorubicin-based concurrent chemoradiation and surgical resection for localized extremity and body wall soft tissue sarcomas
Peter W T Pisters, Shreyaskumar R Patel, Victor G Prieto, et al.
Annals of Epidemiology
|
December 15, 2021
The Millennium Cohort Study: The first 20 years of research dedicated to understanding the long-term health of US Service Members and Veterans
Jennifer N Belding, Sheila F Castañeda, Isabel G Jacobson, et al.
American Journal of Human Genetics
|
February 18, 2004
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease
Gonçalo R Abecasis, Beverly M Yashar, Yu Zhao, et al.
Human Molecular Genetics
|
April 4, 2017
REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival
Shobi Veleri, Jacob Nellissery, Bibhudatta Mishra, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 24, 2008
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
Artur V Cideciyan, Tomas S Aleman, Sanford L Boye, et al.
Page
of 68