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Medycyna Wieku Rozwojowego|June 18, 2003
[The principles of molecular diagnosis of recessive forms of prelingual non-syndromic hearing loss]Joanna Wiszniewska, Wojciech Wiszniewski, Jerzy BalHuman Genetics|February 1, 2007
Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for the visual phenotype in the original report of uniparental disomy 14Wojciech Wiszniewski, Richard Alan Lewis, James R LupskiHuman Genetics|May 20, 2011
Genomic medicine and neurological diseasePhilip M Boone, Wojciech Wiszniewski, James R LupskiJournal of Clinical Neuromuscular Disease|November 20, 2015
Expanding Phenotype of VRK1 Mutations in Motor Neuron DiseaseThy P Nguyen, Suur Biliciler, Wojciech Wiszniewski, et al.Medycyna Wieku Rozwojowego|June 18, 2003
[Identification of T274I mutation in the SMN1 gene in a patient with spinal muscular atrophy]Maria Jedrzejowska, Wojciech Wiszniewski, Barbara Ryniewicz, et al.Journal of Neurology|May 14, 2020
Screening for genetic mutations in patients with neuropathy without definite etiology is usefulBraden Vogt, Nizar Chahin, Wojciech Wiszniewski, et al.Journal of Molecular Evolution|February 8, 2005
Evolution of ABCA4 proteins in vertebratesAlexander N Yatsenko, Wojciech Wiszniewski, Charles M Zaremba, et al.American Journal of Human Genetics|October 28, 2005
Curcumin treatment abrogates endoplasmic reticulum retention and aggregation-induced apoptosis associated with neuropathy-causing myelin protein zero-truncating mutantsMehrdad Khajavi, Ken Inoue, Wojciech Wiszniewski, et al.Human Molecular Genetics|July 13, 2013
Curcumin facilitates a transitory cellular stress response in Trembler-J miceYuji Okamoto, Davut Pehlivan, Wojciech Wiszniewski, et al.Human Genetics|December 15, 2010
Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosisWojciech Wiszniewski, Richard Alan Lewis, David W Stockton, et al.Pageof 6