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M Ozguc

Showing results (1-10 of 8) with videos related to

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Human 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.
Experimental Cell Research|June 1, 2005
Myogenic program induction in mature fat tissue (with MyoD expression)Y C Kocaefe, D Israeli, M Ozguc, 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.
Biochimica Et Biophysica Acta|May 29, 1981
Effect of piracetam on sickle erythrocytes and sickle hemoglobinT Asakura, S T Ohnishi, K Adachi, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish populationE Yilmaz, S Ozen, B Balci, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1980
Effect of cetiedil on erythrocyte sickling: new type of antisickling agent that may affect erythrocyte membranesT Asakura, S T Ohnishi, K Adachi, et al.
American Journal of Human Genetics|March 21, 2000
Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtelM Topçu, C Gartioux, F Ribierre, 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

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Human 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.
Experimental Cell Research|June 1, 2005
Myogenic program induction in mature fat tissue (with MyoD expression)Y C Kocaefe, D Israeli, M Ozguc, 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.
Biochimica Et Biophysica Acta|May 29, 1981
Effect of piracetam on sickle erythrocytes and sickle hemoglobinT Asakura, S T Ohnishi, K Adachi, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish populationE Yilmaz, S Ozen, B Balci, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1980
Effect of cetiedil on erythrocyte sickling: new type of antisickling agent that may affect erythrocyte membranesT Asakura, S T Ohnishi, K Adachi, et al.
American Journal of Human Genetics|March 21, 2000
Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtelM Topçu, C Gartioux, F Ribierre, 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