Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lenka, Ivings"'
Autor:
Lenka Ivings, Martin McKibbin, Uwe Wolfrum, Erwin van Wijk, Ferry F.J. Kersten, Bert van der Zwaag, Michael E. Cheetham, Tim M. Strom, G. A. Williams, Sylvia E. C. van Beersum, Chris F. Inglehearn, Sharola Dharmaraj, Marius Ueffing, Tina Sedmak, Frans P.M. Cremers, C. Geoff Woods, Joris A. Veltman, Marijke N. Zonneveld, Moin Mohamed, Karsten Boldt, Ronald Roepman, Heleen H. Arts, Irene H. Maumenee, Kerstin Nagel-Wolfrum, Irma Lopez, Hussain Jafri, Yasmin Rashid, Monika Beer, Ilse Gosens, Anneke I. den Hollander, Katherine V. Towns, Kelly Springell, Robert K. Koenekoop
Publikováno v:
Nature Genetics, 39, 7, pp. 889-95
Nature Genetics, 39, 889-95
Nature Genetics, 39, 889-95
Contains fulltext : 53618.pdf (Publisher’s version ) (Closed access) Leber congenital amaurosis (LCA) causes blindness or severe visual impairment at or within a few months of birth. Here we show, using homozygosity mapping, that the LCA5 gene on c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eb62f5f5c7163ad762001380759bbc0
https://doi.org/10.1038/ng2066
https://doi.org/10.1038/ng2066
Autor:
Robert D. Burgoyne, Alexei V. Tepikin, Michael C. Ashby, Lenka Ivings, Dermott W. O'Callaghan, Jamie L. Weiss
Publikováno v:
Journal of Biological Chemistry. 277:14227-14237
The localizations of three members of the neuronal calcium sensor (NCS) family were studied in HeLa cells. Using hippocalcin-EYFP and NCS-1-ECFP, it was found that their localization differed dramatically in resting cells. NCS-1 had a distinct predom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::384af509ecb2e547316d4521d12f0eeb
https://doi.org/10.1074/jbc.m111750200
https://doi.org/10.1074/jbc.m111750200
Autor:
Lenka, Ivings, Katherine V, Towns, M A, Matin, Charles, Taylor, Frederique, Ponchel, Richard J, Grainger, Rajkumar S, Ramesar, David A, Mackey, Chris F, Inglehearn
Publikováno v:
Molecular Vision
Purpose Retinitis pigmentosa (RP) is caused by mutations in a variety of genes, most of which have known functions in the retina. However, one of the most perplexing findings of recent retinal genetics research was the discovery of mutations causing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7404f5dc25569c3c276234e2e5681c8e
https://pubmed.ncbi.nlm.nih.gov/19096719
https://pubmed.ncbi.nlm.nih.gov/19096719
Publikováno v:
The Biochemical journal. 363(Pt 3)
The neuronal calcium sensors are a family of EF-hand-containing Ca(2+)-binding proteins expressed predominantly in retinal photoreceptors and neurons. One of the family members is neurocalcin delta, the function of which is unknown. As an approach to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4184f785f9cb41eef48dc6a23dedd125
https://pubmed.ncbi.nlm.nih.gov/11964161
https://pubmed.ncbi.nlm.nih.gov/11964161