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Behavioural Neurology|January 31, 2017
Mice with Catalytically Inactive Cathepsin A Display Neurobehavioral AlterationsO Y Calhan, V SeyrantepeDiagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|June 13, 2000
Diagnosis of quantitative mitochondrial DNA defects by rapidly prepared whole mitochondrial DNA probeV Seyrantepe, H TopalogluHuman Mutation|April 29, 1999
Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Mutation in brief no. 235. OnlineV Seyrantepe, M Ozguc, T Coskun, et al.Brain & Development|September 16, 1999
Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibersV Seyrantepe, G Kale, H Topaloglu, et al.Pediatric Neurology|July 3, 1998
mtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girlH Topaloğlu, V Seyrantepe, N Kandemir, et al.Acta Paediatrica (Oslo, Norway : 1992)|March 26, 2003
Wolfram (DIDMOAD) syndrome: a multidisciplinary clinical study in nine Turkish patients and review of the literatureE Simsek, T Simsek, S Tekgül, et al.Eye (London, England)|May 8, 2001
Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy populationC F Dogulu, T Kansu, V Seyrantepe, et al.The Journal of Biological Chemistry|September 26, 2001
Intracellular distribution of lysosomal sialidase is controlled by the internalization signal in its cytoplasmic tailK E Lukong, V Seyrantepe, K Landry, et al.Cell Death and Differentiation|August 5, 2006
Altered gene expression in cells from patients with lysosomal storage disorders suggests impairment of the ubiquitin pathwayP Bifsha, K Landry, L Ashmarina, et al.Human Genetics|September 1, 1997
The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samplesF Calì, I Dianzani, L R Desviat, et al.Pageof 1