About: The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1999 (uk) im September 1999 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q58277705-F5F095E9-0339-4029-8580-BF802DFF9758
publication date	1999-09-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q58277705-6234B3A0-F415-433D-AC15-1BED7A646C54 wds:Q58277705-93FEED0C-2FB4-49A5-BC16-29CE7654F827 wds:Q58277705-BB05D6C5-6C4D-40B0-884D-81B14A56CD2D wds:Q58277705-DEF036A9-006D-4A86-A84A-CD02DF9EAF7A
author name string	Kang Zhang Rando Allikmets Min Han Marina Kniazeva
rdfs:label	The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration (en) The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration (nl)
skos:prefLabel	The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration (en) The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration (nl)
name	The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration (en) The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration (nl)
author	wds:Q58277705-33871CAC-215F-4498-8DCF-ED26BB3B04B2 wds:Q58277705-DB035D08-E88F-4AF7-9C07-2B6F155AAD90
author	Amy Hutchinson Michael Dean
title	wds:Q58277705-7DA0BD59-A7AE-4CA1-9840-98751383F6B8
title	The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration (en)
page(s)	wds:Q58277705-43EF9163-936D-4249-A2C5-67CA4FA05728
page(s)	234-237
instance of	wds:Q58277705-378A8E88-E8AB-4A21-B4C6-10896BB1B032
instance of	scholarly article
main subject	wds:Q58277705-12D2AAE7-DCF2-42A1-B8C3-EEAEA82414F6
main subject	macular degeneration
PubMed ID	wds:Q58277705-88661135-B791-4037-9D0C-3EB451F2363F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10486215
PubMed ID	10486215
published in	wds:Q58277705-DA8E1F43-63EC-4C82-A89B-75F36677E2BA
published in	Genomics
issue	wds:Q58277705-04B96D3C-83F6-4E7B-839F-3F6EF367057F
volume	wds:Q58277705-87A16BDC-A93F-4408-8B9E-D2AAA05FA599
issue	2
volume	60
DOI	wds:Q58277705-2EFB11FC-EE82-4A69-8105-09D3553B028F
DOI	http://dx.doi.org/10.1006/GENO.1999.5896
DOI	10.1006/GENO.1999.5896
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58277705
is cites work of	The molecular genetics of familial intrahepatic cholestasis Autosomal dominant Stargardt-like macular dystrophy Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa The influence of genetics on response to treatment with ranibizumab (Lucentis) for age-related macular degeneration: the Lucentis Genotype Study (an American Ophthalmological Society thesis). ABC-me: a novel mitochondrial transporter induced by GATA-1 during erythroid differentiation Genetic factors of age-related macular degeneration Retinal very long-chain PUFAs: new insights from studies on ELOVL4 protein Fluorescent pigments of the retinal pigment epithelium and age-related macular degeneration Review of genetics in age related macular degeneration. Interaction of extracellular domain 2 of the human retina-specific ATP-binding cassette transporter (ABCA4) with all-trans-retinal The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene Retinoid binding properties of nucleotide binding domain 1 of the Stargardt disease-associated ATP binding cassette (ABC) transporter, ABCA4. The clinical spectrum of inherited diseases involved in the synthesis and remodeling of complex lipids. A tentative overview AMD and the alternative complement pathway: genetics and functional implications Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario. Genetic modifiers and oligogenic inheritance Genetic risk factors and age-related macular degeneration (AMD). Evaluation of macular abnormalities in Stargardt's disease using optical coherence tomography and scanning laser ophthalmoscope microperimetry Analysis of six candidate genes as potential modifiers of disease expression in canine XLPRA1, a model for human X-linked retinitis pigmentosa 3 Stargadt's disease in two Nigerian siblings Stargardt macular dystrophy: common ABCA4 mutations in South Africa--establishment of a rapid genetic test and relating risk to patients Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles. Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease. Genetic screening for macular dystrophies in patients clinically diagnosed with dry age-related macular degeneration
is cites work of	wds:Q24670001-82368F5C-BDB1-48C3-9C9C-F7CCFAD96CBD wds:Q33911373-31913771-547E-464C-87AC-33222B858051 wds:Q35676416-C64EDB46-B782-4089-951F-D7114B627655 wds:Q38270108-2757CA80-843C-4DEC-AF56-9AEBDEF063FF wds:Q45198203-3832DF4F-F6F7-452B-A527-92C96C0AE47D wds:Q55551541-DAF74A00-F81B-4C87-A9DB-C8729624D087 wds:Q26744106-129AC9A9-ED2D-45D4-B720-E5D2B196FC27 wds:Q41130648-1F8DBF90-0A04-4E5A-8F9A-78CCEB8E94F1 wds:Q35749765-BF9128D5-7BF8-4BEE-9B42-67E144CEA8BD wds:Q34385985-EBB3A07E-0BED-4DCD-8339-BF4D0268FB51 wds:Q38511788-0CAEE7BA-7B64-4A13-899C-BDFF20DE42EC wds:Q38335210-CF58F05B-9F75-49DE-8AF8-763DDCFFF19E wds:Q33291736-25992F74-C7C4-4892-9EE3-819674036D02 wds:Q35745250-D05E189D-0B64-4A1F-A296-E31575621FD6 wds:Q55359814-0F9B6A20-86D9-47B7-BD05-4BD0DCD3CD52 wds:Q34286193-9FE4EBDA-74FA-4EB3-930A-F39CF9A2EFDA wds:Q22254182-85A2545E-6E35-4546-B334-A43597B32F76 wds:Q33378564-7FF07871-CB83-45C6-A10E-734222D8B7AB wds:Q34369282-C81F2E4E-1746-40BF-BC07-FEF1FDBBC43B wds:Q36492749-6968FFA3-CD8C-411A-B8DE-EC07D26FA3B6 wds:Q63536992-D7B9C62F-3F45-4CFD-A7B0-20067BB26E4D wds:Q37039797-C2D8394B-5583-413D-930A-E02561A6F740 wds:Q33902007-E541BA06-348A-4D56-9BCD-314CCAAB8558 wds:Q53155688-27FAB65F-3D1B-456A-A59B-13AFC237154B

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