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  • 1-8 ل  8 نتائج ل ""Photoreceptor Cells, Vertebrate""

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Publisher : nature pub. co
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Academic Journal

AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis.

  • Authors : Louie CM; Howard Hughes Medical Institute, Department of Pediatrics, University of California, San Diego, La Jolla, USA.; Caridi G

Subjects: Photoreceptor Cells, Vertebrate/Photoreceptor Cells, Vertebrate/Photoreceptor Cells, Vertebrate/*pathology ; Proto-Oncogene Proteins/Proto-Oncogene Proteins/Proto-Oncogene Proteins/*metabolism ; Retinal Degeneration/Retinal Degeneration/Retinal Degeneration/*pathology

  • Source: Nature genetics [Nat Genet] 2010 Feb; Vol. 42 (2), pp. 175-80. Date of Electronic Publication: 2010 Jan 17.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited

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Academic Journal

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy.

  • Authors : Otto EA; Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan, USA.; Hurd TW

Subjects: Genetic Association Studies*; Autoantigens/Autoantigens/Autoantigens/*genetics ; Exons/Exons/Exons/*genetics

  • Source: Nature genetics [Nat Genet] 2010 Oct; Vol. 42 (10), pp. 840-50. Date of Electronic Publication: 2010 Sep 12.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited

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Academic Journal

Blindness and auditory impairment caused by loss of the sodium bicarbonate cotransporter NBC3.

  • Authors : Bok D; Department of Neurobiology, Jules Stein Eye Institute, Los Angeles, California, 90095, USA.; Galbraith G

Subjects: Auditory Perceptual Disorders/Auditory Perceptual Disorders/Auditory Perceptual Disorders/*etiology ; Blindness/Blindness/Blindness/*etiology ; Sodium-Bicarbonate Symporters/Sodium-Bicarbonate Symporters/Sodium-Bicarbonate Symporters/*deficiency

  • Source: Nature genetics [Nat Genet] 2003 Jul; Vol. 34 (3), pp. 313-9.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium:

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Academic Journal

Protection of Rpe65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degeneration.

  • Authors : Grimm C; Laboratory of Retinal Cell Biology, Department of Ophthalmology, University Hospital Zurich, Zurich, Switzerland. ; Wenzel A

Subjects: Light/Light/Light/*adverse effects ; Pigment Epithelium of Eye/Pigment Epithelium of Eye/Pigment Epithelium of Eye/*radiation effects ; Proteins/Proteins/Proteins/*genetics

  • Source: Nature genetics [Nat Genet] 2000 May; Vol. 25 (1), pp. 63-6.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium:

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Academic Journal

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

  • Authors : Furukawa T; Department of Genetics and Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts, USA. ; Morrow EM

Subjects: Circadian Rhythm/Circadian Rhythm/Circadian Rhythm/*genetics ; Homeodomain Proteins/Homeodomain Proteins/Homeodomain Proteins/*genetics ; Retinal Diseases/Retinal Diseases/Retinal Diseases/*genetics

  • Source: Nature genetics [Nat Genet] 1999 Dec; Vol. 23 (4), pp. 466-70.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium:

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Academic Journal

Evidence for two apoptotic pathways in light-induced retinal degeneration.

  • Authors : Hao W; Division of Biology, California Institute of Technology, Pasadena, California 91125, USA.; Wenzel A

Subjects: Apoptosis* ; Eye Proteins*; Light/Light/Light/*adverse effects

  • Source: Nature genetics [Nat Genet] 2002 Oct; Vol. 32 (2), pp. 254-60. Date of Electronic Publication: 2002 Sep 03.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited

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Academic Journal

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

  • Authors : Sohocki MM; Human Genetics Center, School of Public Health, The University of Texas-Houston Health Science Center, Houston, Texas, USA.; Bowne SJ

Subjects: Chromosomes, Human, Pair 17* ; Mutation*; Carrier Proteins/Carrier Proteins/Carrier Proteins/*genetics

  • Source: Nature genetics [Nat Genet] 2000 Jan; Vol. 24 (1), pp. 79-83.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium:

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Academic Journal

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa.

  • Authors : Pierce EA; F.M. Kirby Center for Molecular Ophthalmology, University of Pennsylvania, Scheie Eye Institute, Philadelphia, USA. ; Quinn T

Subjects: Mutation*; Eye Proteins/Eye Proteins/Eye Proteins/*genetics ; Photoreceptor Cells, Vertebrate/Photoreceptor Cells, Vertebrate/Photoreceptor Cells, Vertebrate/*metabolism

  • Source: Nature genetics [Nat Genet] 1999 Jul; Vol. 22 (3), pp. 248-54.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium:

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  • 1-8 ل  8 نتائج ل ""Photoreceptor Cells, Vertebrate""