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Yelena Bykhovskaya

Showing results (1-10 of 29) with videos related to

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Experimental Eye Research|December 14, 2020
Update on the genetics of keratoconusYelena Bykhovskaya, Yaron S Rabinowitz
Molecular Genetics and Metabolism|June 2, 2009
Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteinsYelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Molecular Genetics and Metabolism|March 22, 2007
Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Eye and Vision (London, England)|June 29, 2016
Genetics in Keratoconus: where are we?Yelena Bykhovskaya, Benjamin Margines, Yaron S Rabinowitz
International Journal of Keratoconus and Ectatic Corneal Diseases|October 10, 2017
Abnormal regulation of extracellular matrix and adhesion molecules in corneas of patients with keratoconusYelena Bykhovskaya, Anastasia Gromova, Helen P Makarenkova, et al.
American Journal of Human Genetics|April 27, 2004
Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Kari Casas, Emebet Mengesha, et al.
The Journal of Biological Chemistry|March 18, 2005
Mitochondrial myopathy and sideroblastic anemia (MLASA): missense mutation in the pseudouridine synthase 1 (PUS1) gene is associated with the loss of tRNA pseudouridylationJeffrey R Patton, Yelena Bykhovskaya, Emebet Mengesha, et al.
Ophthalmic Genetics|October 22, 2013
C.57 C > T Mutation in MIR 184 is Responsible for Congenital Cataracts and Corneal Abnormalities in a Five-generation Family from Galicia, SpainYelena Bykhovskaya, Ana L Caiado Canedo, Kenneth W Wright, et al.
Journal of Refractive Surgery (Thorofare, N.J. : 1995)|April 26, 2014
Optical coherence tomography combined with videokeratography to differentiate mild keratoconus subtypesYaron S Rabinowitz, Xiaohui Li, Ana Laura Caiado Canedo, et al.
Molecular Genetics and Metabolism|April 28, 2004
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutationYelena Bykhovskaya, Emebet Mengesha, Dai Wang, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Experimental Eye Research|December 14, 2020
Update on the genetics of keratoconusYelena Bykhovskaya, Yaron S Rabinowitz
Molecular Genetics and Metabolism|June 2, 2009
Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteinsYelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Molecular Genetics and Metabolism|March 22, 2007
Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Eye and Vision (London, England)|June 29, 2016
Genetics in Keratoconus: where are we?Yelena Bykhovskaya, Benjamin Margines, Yaron S Rabinowitz
International Journal of Keratoconus and Ectatic Corneal Diseases|October 10, 2017
Abnormal regulation of extracellular matrix and adhesion molecules in corneas of patients with keratoconusYelena Bykhovskaya, Anastasia Gromova, Helen P Makarenkova, et al.
American Journal of Human Genetics|April 27, 2004
Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Kari Casas, Emebet Mengesha, et al.
The Journal of Biological Chemistry|March 18, 2005
Mitochondrial myopathy and sideroblastic anemia (MLASA): missense mutation in the pseudouridine synthase 1 (PUS1) gene is associated with the loss of tRNA pseudouridylationJeffrey R Patton, Yelena Bykhovskaya, Emebet Mengesha, et al.
Ophthalmic Genetics|October 22, 2013
C.57 C > T Mutation in MIR 184 is Responsible for Congenital Cataracts and Corneal Abnormalities in a Five-generation Family from Galicia, SpainYelena Bykhovskaya, Ana L Caiado Canedo, Kenneth W Wright, et al.
Journal of Refractive Surgery (Thorofare, N.J. : 1995)|April 26, 2014
Optical coherence tomography combined with videokeratography to differentiate mild keratoconus subtypesYaron S Rabinowitz, Xiaohui Li, Ana Laura Caiado Canedo, et al.
Molecular Genetics and Metabolism|April 28, 2004
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutationYelena Bykhovskaya, Emebet Mengesha, Dai Wang, et al.
Pageof 3