检索结果 - Samuel G. Jacobson

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  1. 1
    Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

    Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration 由 Samuel G. Jacobson

    出版 2004
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  2. 2
    Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations

    Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations 由 Samuel G. Jacobson

    出版 2011
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  3. 3
    Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

    Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination 由 Samuel G. Jacobson

    出版 2003
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  4. 4
    Altered thermal sensitivity in injured and demyelinated nerve: A possible model of temperature effects in multiple sclerosis

    Altered thermal sensitivity in injured and demyelinated nerve: A possible model of temperature effects in multiple sclerosis 由 Floyd A. Davis, Samuel G. Jacobson

    出版 1971
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  5. 5
    An Alternative Phototransduction Model for Human Rod and Cone ERG a-waves: Normal Parameters and Variation with Age

    An Alternative Phototransduction Model for Human Rod and Cone ERG a-waves: Normal Parameters and Variation with Age 由 Artur V. Cideciyan, Samuel G. Jacobson

    出版 1996
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  6. 6
    Leber Congenital Amaurosis (LCA): Potential for Improvement of Vision

    Leber Congenital Amaurosis (LCA): Potential for Improvement of Vision 由 Artur V. Cideciyan, Samuel G. Jacobson

    出版 2019
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  7. 7
    Development of visual acuity in infants with congenital cataracts.

    Development of visual acuity in infants with congenital cataracts. 由 Samuel G. Jacobson, Indra Mohindra, Richard Held

    出版 1981
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  8. 8
    Autofluorescence Imaging With Near-Infrared Excitation: Normalization by Reflectance to Reduce Signal From Choroidal Fluorophores

    Autofluorescence Imaging With Near-Infrared Excitation: Normalization by Reflectance to Reduce Signal From Choroidal Fluorophores 由 Artur V. Cideciyan, Małgorzata Świder, Samuel G. Jacobson

    出版 2015
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  9. 9
    Autosomal Dominant Retinitis Pigmentosa Caused by the Threonine-17-Methionine Rhodopsin Mutation: Retinal Histopathology and Immunocytochemistry

    Autosomal Dominant Retinitis Pigmentosa Caused by the Threonine-17-Methionine Rhodopsin Mutation: Retinal Histopathology and Immunocytochemistry 由 Zong-Yi Li, Samuel G. Jacobson, Ann H. Milam

    出版 1994
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  10. 10
    Retinal Pigment Epithelium Defects in Humans and Mice with Mutations in<i>MYO7A</i>: Imaging Melanosome-Specific Autofluorescence

    Retinal Pigment Epithelium Defects in Humans and Mice with Mutations in<i>MYO7A</i>: Imaging Melanosome-Specific Autofluorescence 由 Daniel Gibbs, Artur V. Cideciyan, Samuel G. Jacobson, David S. Williams

    出版 2009
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  11. 11
    Retinal Function and Rhodopsin Levels in Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Mutations

    Retinal Function and Rhodopsin Levels in Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Mutations 由 Samuel G. Jacobson, C.M. Kemp, Ching-Hwa Sung, Jeremy Nathans

    出版 1991
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  12. 12
    Enhanced S cone syndrome: Evidence for an abnormally large number of S cones

    Enhanced S cone syndrome: Evidence for an abnormally large number of S cones 由 Donald C. Hood, Artur V. Cideciyan, Alejandro J. Román, Samuel G. Jacobson

    出版 1995
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  13. 13
    Predicting Progression of<i>ABCA4</i>-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front

    Predicting Progression of<i>ABCA4</i>-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front 由 Artur V. Cideciyan, Małgorzata Świder, Sharon Schwartz, Edwin M. Stone, Samuel G. Jacobson

    出版 2015
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  14. 14
    Abnormal Rod Dark Adaptation in Autosomal Dominant Retinitis Pigmentosa With Proline-23-Histidine Rhodopsin Mutation

    Abnormal Rod Dark Adaptation in Autosomal Dominant Retinitis Pigmentosa With Proline-23-Histidine Rhodopsin Mutation 由 C.M. Kemp, Samuel G. Jacobson, Alejandro J. Román, Ching-Hwa Sung, Jeremy Nathans

    出版 1992
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  15. 15
    In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development

    In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development 由 Hong Cheng, Tomas S. Alemán, Artur V. Cideciyan, Ritu Khanna, Samuel G. Jacobson, Anand Swaroop

    出版 2006
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  16. 16
    Full-field stimulus testing: Role in the clinic and as an outcome measure in clinical trials of severe childhood retinal disease

    Full-field stimulus testing: Role in the clinic and as an outcome measure in clinical trials of severe childhood retinal disease 由 Alejandro J. Román, Artur V. Cideciyan, Vivian Wu, Alexandra V. Garafalo, Samuel G. Jacobson

    出版 2021
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  17. 17
    Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man

    Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man 由 Artur V. Cideciyan, Xinyu Zhao, Lori Nielsen, Shahrokh C. Khani, Samuel G. Jacobson, Krzysztof Palczewski

    出版 1998
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  18. 18
    Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate

    Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate 由 Tadao Maeda, Artur V. Cideciyan, Akiko Maeda, Marcin Golczak, T. S. Aleman, Samuel G. Jacobson, Krzysztof Palczewski

    出版 2009
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  19. 19
    Relatively Enhanced S Cone Function in the Goldmann-Favre Syndrome

    Relatively Enhanced S Cone Function in the Goldmann-Favre Syndrome 由 Samuel G. Jacobson, Alejandro J. Román, Marisa I. Román, J. Donald M. Gass, J. A. Parker

    出版 1991
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  20. 20
    Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia

    Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia 由 Susanne Kohl, Britta Baumann, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Maria Vadalà, Samuel G. Jacobson, Bernd Wissinger

    出版 2002
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