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Gökhan Yigit

Showing results (1-10 of 76) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Cellular models and therapeutic perspectives in hypertrophic cardiomyopathyGökhan Yigit, Bernd Wollnik
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 10, 2025
Understanding inherited cardiomyopathies: clinical aspects and genetic determinantsGökhan Yigit, Silke Kaulfuß, Bernd Wollnik
Molecular Genetics and Metabolism Reports|December 6, 2023
Lysinuric protein intolerance caused by a homozygous <i>SLC7A7</i> deletion and presented with hyperferritinemia and osteoporosis in two siblingsIrem Kalay, Hüseyin Aykut, Zuhal Caliskan, et al.
Cell Communication and Signaling : CCS|April 5, 2012
Epstein-Barr virus LMP2A signaling in statu nascendi mimics a B cell antigen receptor-like activation signalNiklas Engels, Gökhan Yigit, Christoph H Emmerich, et al.
American Journal of Medical Genetics. Part A|September 12, 2020
Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATMSimone Schröder, Britta Wieland, Andreas Ohlenbusch, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type IEsra Kilic, Gökhan Yigit, Gülen Eda Utine, et al.
American Journal of Medical Genetics. Part A|October 13, 2021
Genomic basis of syndromic short stature in an Algerian patient cohortShahida Moosa, Farida Chentli, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|October 19, 2016
Smith-Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicismShahida Moosa, Helena Böhrer-Rabel, Janine Altmüller, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Novel compound heterozygous mutations in <i>TELO2</i> in a patient with severe expression of You-Hoover-Fong syndromeShahida Moosa, Janine Altmüller, Troels Lyngbye, et al.
American Journal of Medical Genetics. Part A|August 18, 2016
An unusual presentation of Kabuki syndrome with orbital cysts, microphthalmia, and cholestasis with bile duct paucityNina Bögershausen, Umut Altunoglu, Filippo Beleggia, et al.
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Cellular models and therapeutic perspectives in hypertrophic cardiomyopathyGökhan Yigit, Bernd Wollnik
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 10, 2025
Understanding inherited cardiomyopathies: clinical aspects and genetic determinantsGökhan Yigit, Silke Kaulfuß, Bernd Wollnik
Molecular Genetics and Metabolism Reports|December 6, 2023
Lysinuric protein intolerance caused by a homozygous <i>SLC7A7</i> deletion and presented with hyperferritinemia and osteoporosis in two siblingsIrem Kalay, Hüseyin Aykut, Zuhal Caliskan, et al.
Cell Communication and Signaling : CCS|April 5, 2012
Epstein-Barr virus LMP2A signaling in statu nascendi mimics a B cell antigen receptor-like activation signalNiklas Engels, Gökhan Yigit, Christoph H Emmerich, et al.
American Journal of Medical Genetics. Part A|September 12, 2020
Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATMSimone Schröder, Britta Wieland, Andreas Ohlenbusch, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type IEsra Kilic, Gökhan Yigit, Gülen Eda Utine, et al.
American Journal of Medical Genetics. Part A|October 13, 2021
Genomic basis of syndromic short stature in an Algerian patient cohortShahida Moosa, Farida Chentli, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|October 19, 2016
Smith-Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicismShahida Moosa, Helena Böhrer-Rabel, Janine Altmüller, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Novel compound heterozygous mutations in <i>TELO2</i> in a patient with severe expression of You-Hoover-Fong syndromeShahida Moosa, Janine Altmüller, Troels Lyngbye, et al.
American Journal of Medical Genetics. Part A|August 18, 2016
An unusual presentation of Kabuki syndrome with orbital cysts, microphthalmia, and cholestasis with bile duct paucityNina Bögershausen, Umut Altunoglu, Filippo Beleggia, et al.
Pageof 8