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Plos One
|
June 19, 2008
UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle?
Shira Amsili, Hagit Zer, Stephan Hinderlich, et al.
Human Molecular Genetics
|
February 4, 2014
Gne depletion during zebrafish development impairs skeletal muscle structure and function
Alon Daya, Gad David Vatine, Michal Becker-Cohen, et al.
International Journal of Molecular Sciences
|
September 29, 2020
Macular Ganglion Cell Complex and Peripapillary Retinal Nerve Fiber Layer Thinning in Patients with Type-1 Gaucher Disease
Yishay Weill, Ari Zimran, David Zadok, et al.
International Journal of Molecular Sciences
|
June 13, 2025
Olfactory Perception in Parkinson's Disease: The Impact of <i>GBA1</i> Variants (Sidransky Syndrome)
Mikhal E Cohen, Yosef Shechter, Melania Dominko, et al.
Journal of Receptor and Signal Transduction Research
|
December 17, 2014
Survival-apoptosis associated signaling in GNE myopathy-cultured myoblasts
Avi Harazi, Malka Chaouat, Zippora Shlomai, et al.
Journal of Neuromuscular Diseases
|
January 28, 2020
Upregulation of Hallmark Muscle Genes Protects GneM743T/M743T Mutated Knock-In Mice From Kidney and Muscle Phenotype
Hadar Benyamini, Yehuda Kling, Lena Yakovlev, et al.
Journal of Clinical Medicine
|
October 17, 2019
Long Term Follow-Up of 103 Untreated Adult Patients with Type 1 Gaucher Disease
Tama Dinur, Ari Zimran, Michal Becker-Cohen, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Contribution of Glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in Patients with Gaucher Disease
Tama Dinur, Peter Bauer, Christian Beetz, et al.
Neuromolecular Medicine
|
December 15, 2012
Variable phenotypes of knockin mice carrying the M712T Gne mutation
Ilan Sela, Lena Yakovlev, Michal Becker Cohen, et al.
Plos One
|
July 30, 2013
Variable myopathic presentation in a single family with novel skeletal RYR1 mutation
Ruben Attali, Sharon Aharoni, Susan Treves, et al.
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Search research articles
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Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Plos One
|
June 19, 2008
UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle?
Shira Amsili, Hagit Zer, Stephan Hinderlich, et al.
Human Molecular Genetics
|
February 4, 2014
Gne depletion during zebrafish development impairs skeletal muscle structure and function
Alon Daya, Gad David Vatine, Michal Becker-Cohen, et al.
International Journal of Molecular Sciences
|
September 29, 2020
Macular Ganglion Cell Complex and Peripapillary Retinal Nerve Fiber Layer Thinning in Patients with Type-1 Gaucher Disease
Yishay Weill, Ari Zimran, David Zadok, et al.
International Journal of Molecular Sciences
|
June 13, 2025
Olfactory Perception in Parkinson's Disease: The Impact of <i>GBA1</i> Variants (Sidransky Syndrome)
Mikhal E Cohen, Yosef Shechter, Melania Dominko, et al.
Journal of Receptor and Signal Transduction Research
|
December 17, 2014
Survival-apoptosis associated signaling in GNE myopathy-cultured myoblasts
Avi Harazi, Malka Chaouat, Zippora Shlomai, et al.
Journal of Neuromuscular Diseases
|
January 28, 2020
Upregulation of Hallmark Muscle Genes Protects GneM743T/M743T Mutated Knock-In Mice From Kidney and Muscle Phenotype
Hadar Benyamini, Yehuda Kling, Lena Yakovlev, et al.
Journal of Clinical Medicine
|
October 17, 2019
Long Term Follow-Up of 103 Untreated Adult Patients with Type 1 Gaucher Disease
Tama Dinur, Ari Zimran, Michal Becker-Cohen, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Contribution of Glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in Patients with Gaucher Disease
Tama Dinur, Peter Bauer, Christian Beetz, et al.
Neuromolecular Medicine
|
December 15, 2012
Variable phenotypes of knockin mice carrying the M712T Gne mutation
Ilan Sela, Lena Yakovlev, Michal Becker Cohen, et al.
Plos One
|
July 30, 2013
Variable myopathic presentation in a single family with novel skeletal RYR1 mutation
Ruben Attali, Sharon Aharoni, Susan Treves, et al.
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of 4