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RNA Biology|February 21, 2022
Background splicing as a predictor of aberrant splicing in genetic diseaseDiana Alexieva, Yi Long, Rupa Sarkar, et al.Clinical and Experimental Nephrology|November 20, 2015
X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 geneXue Jun Fu, Kandai Nozu, Aya Eguchi, et al.Pediatric Nephrology (Berlin, Germany)|March 18, 2014
Natural history of genetically proven autosomal recessive Alport syndromeMasafumi Oka, Kandai Nozu, Hiroshi Kaito, et al.Molecular Genetics & Genomic Medicine|May 27, 2017
A birth of bipartite exon by intragenic deletionKandai Nozu, Kazumoto Iijima, Toru Igarashi, et al.Journal of Human Genetics|October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndromeKandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.Clinical Journal of the American Society of Nephrology : CJASN|September 4, 2014
X-linked Alport syndrome caused by splicing mutations in COL4A5Kandai Nozu, Igor Vorechovsky, Hiroshi Kaito, et al.Journal of Human Genetics|March 10, 2017
Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosisKandai Nozu, Shogo Minamikawa, Shiro Yamada, et al.Human Molecular Genetics|March 5, 2002
Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locusKati Asumalahti, Colin Veal, Tarja Laitinen, et al.Pageof 4