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Acta Neuropathologica
|
November 23, 2020
Intellectual disability: dendritic anomalies and emerging genetic perspectives
Tam T Quach, Harrison J Stratton, Rajesh Khanna, et al.
The Journal of Biological Chemistry
|
May 1, 2008
Neogenin-mediated hemojuvelin shedding occurs after hemojuvelin traffics to the plasma membrane
An-Sheng Zhang, Fan Yang, Kathrin Meyer, et al.
Neurobiology of Aging
|
May 27, 2021
Amyotrophic lateral sclerosis alters the metabolic aging profile in patient derived fibroblasts
Margarita Gerou, Benjamin Hall, Ryan Woof, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2004
Prevalence of 20S proteasome, anti-nuclear and thyroid antibodies in young patients at onset of type 1 diabetes mellitus and the risk of autoimmune thyroiditis
Olga Kordonouri, Kathrin Meyer, Karl Egerer, et al.
Orphanet Journal of Rare Diseases
|
November 11, 2022
Sex-split analysis of pathology and motor-behavioral outcomes in a mouse model of CLN8-Batten disease reveals an increased disease burden and trajectory in female Cln8<sup>mnd</sup> mice
Andrew D Holmes, Katherine A White, Melissa A Pratt, et al.
Journal of Visualized Experiments : Jove
|
June 28, 2021
In vitro Modeling for Neurological Diseases using Direct Conversion from Fibroblasts to Neuronal Progenitor Cells and Differentiation into Astrocytes
Cassandra N Dennys, Julieth A Sierra-Delgado, Shrestha Sinha Ray, et al.
International Journal of Molecular Sciences
|
November 26, 2022
Neurodegenerative Diseases: From Dysproteostasis, Altered Calcium Signalosome to Selective Neuronal Vulnerability to AAV-Mediated Gene Therapy
Tam T Quach, Harrison J Stratton, Rajesh Khanna, et al.
Biology
|
June 28, 2023
In Vitro Modeling as a Tool for Testing Therapeutics for Spinal Muscular Atrophy and IGHMBP2-Related Disorders
Julieth Andrea Sierra-Delgado, Shrestha Sinha-Ray, Abuzar Kaleem, et al.
Human Molecular Genetics
|
November 18, 2008
Rescue of a severe mouse model for spinal muscular atrophy by U7 snRNA-mediated splicing modulation
Kathrin Meyer, Julien Marquis, Judith Trüb, et al.
Neurobiology of Aging
|
March 8, 2021
Voluntary wheel running with and without follistatin overexpression improves NMJ transmission but not motor unit loss in late life of C57BL/6J mice
Deepti Chugh, Chitra C Iyer, Prameela Bobbili, et al.
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of 7
Search research articles
Search
Showing results (21-30 of 61) with videos related to
Sort By:
Page
of 7
Acta Neuropathologica
|
November 23, 2020
Intellectual disability: dendritic anomalies and emerging genetic perspectives
Tam T Quach, Harrison J Stratton, Rajesh Khanna, et al.
The Journal of Biological Chemistry
|
May 1, 2008
Neogenin-mediated hemojuvelin shedding occurs after hemojuvelin traffics to the plasma membrane
An-Sheng Zhang, Fan Yang, Kathrin Meyer, et al.
Neurobiology of Aging
|
May 27, 2021
Amyotrophic lateral sclerosis alters the metabolic aging profile in patient derived fibroblasts
Margarita Gerou, Benjamin Hall, Ryan Woof, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2004
Prevalence of 20S proteasome, anti-nuclear and thyroid antibodies in young patients at onset of type 1 diabetes mellitus and the risk of autoimmune thyroiditis
Olga Kordonouri, Kathrin Meyer, Karl Egerer, et al.
Orphanet Journal of Rare Diseases
|
November 11, 2022
Sex-split analysis of pathology and motor-behavioral outcomes in a mouse model of CLN8-Batten disease reveals an increased disease burden and trajectory in female Cln8<sup>mnd</sup> mice
Andrew D Holmes, Katherine A White, Melissa A Pratt, et al.
Journal of Visualized Experiments : Jove
|
June 28, 2021
In vitro Modeling for Neurological Diseases using Direct Conversion from Fibroblasts to Neuronal Progenitor Cells and Differentiation into Astrocytes
Cassandra N Dennys, Julieth A Sierra-Delgado, Shrestha Sinha Ray, et al.
International Journal of Molecular Sciences
|
November 26, 2022
Neurodegenerative Diseases: From Dysproteostasis, Altered Calcium Signalosome to Selective Neuronal Vulnerability to AAV-Mediated Gene Therapy
Tam T Quach, Harrison J Stratton, Rajesh Khanna, et al.
Biology
|
June 28, 2023
In Vitro Modeling as a Tool for Testing Therapeutics for Spinal Muscular Atrophy and IGHMBP2-Related Disorders
Julieth Andrea Sierra-Delgado, Shrestha Sinha-Ray, Abuzar Kaleem, et al.
Human Molecular Genetics
|
November 18, 2008
Rescue of a severe mouse model for spinal muscular atrophy by U7 snRNA-mediated splicing modulation
Kathrin Meyer, Julien Marquis, Judith Trüb, et al.
Neurobiology of Aging
|
March 8, 2021
Voluntary wheel running with and without follistatin overexpression improves NMJ transmission but not motor unit loss in late life of C57BL/6J mice
Deepti Chugh, Chitra C Iyer, Prameela Bobbili, et al.
Page
of 7