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Cells
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June 19, 2019
Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington Disease
Libo Yu-Taeger, Janice Stricker-Shaver, Katrin Arnold, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 17, 2021
Pathophysiological interplay between <i>O</i>-GlcNAc transferase and the Machado-Joseph disease protein ataxin-3
Priscila Pereira Sena, Jonasz J Weber, Maxinne Watchon, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 13, 2010
Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytes
Marta Valenza, Valerio Leoni, Joanna M Karasinska, et al.
Cell
|
March 23, 2019
A Diagnosis for All Rare Genetic Diseases: The Horizon and the Next Frontiers
Kym M Boycott, Taila Hartley, Leslie G Biesecker, et al.
Neurology
|
June 19, 2016
Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families
Anne S Soehn, Tim W Rattay, Stefanie Beck-Wödl, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 2, 2012
A novel BACHD transgenic rat exhibits characteristic neuropathological features of Huntington disease
Libo Yu-Taeger, Elisabeth Petrasch-Parwez, Alexander P Osmand, et al.
British Journal of Cancer
|
March 27, 2023
Detection of circulating cell-free HPV DNA of 13 HPV types for patients with cervical cancer as potential biomarker to monitor therapy response and to detect relapse
Suzana Mittelstadt, Olga Kelemen, Jakob Admard, et al.
Orphanet Journal of Rare Diseases
|
June 25, 2026
Implementation of a medical genomics program for rare diseases in Uruguay
Camila Simoes, María Fernanda Domínguez, Soledad Rodriguez, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]
|
March 27, 2020
PET/MRI and genetic intrapatient heterogeneity in head and neck cancers
Kerstin Clasen, Sara Leibfarth, Franz J Hilke, et al.
Annals of Neurology
|
May 4, 2010
First appraisal of brain pathology owing to A30P mutant alpha-synuclein
Kay Seidel, Ludger Schöls, Silke Nuber, et al.
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of 32
Search research articles
Search
Showing results (191-200 of 313) with videos related to
Sort By:
Page
of 32
Cells
|
June 19, 2019
Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington Disease
Libo Yu-Taeger, Janice Stricker-Shaver, Katrin Arnold, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 17, 2021
Pathophysiological interplay between <i>O</i>-GlcNAc transferase and the Machado-Joseph disease protein ataxin-3
Priscila Pereira Sena, Jonasz J Weber, Maxinne Watchon, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 13, 2010
Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytes
Marta Valenza, Valerio Leoni, Joanna M Karasinska, et al.
Cell
|
March 23, 2019
A Diagnosis for All Rare Genetic Diseases: The Horizon and the Next Frontiers
Kym M Boycott, Taila Hartley, Leslie G Biesecker, et al.
Neurology
|
June 19, 2016
Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families
Anne S Soehn, Tim W Rattay, Stefanie Beck-Wödl, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 2, 2012
A novel BACHD transgenic rat exhibits characteristic neuropathological features of Huntington disease
Libo Yu-Taeger, Elisabeth Petrasch-Parwez, Alexander P Osmand, et al.
British Journal of Cancer
|
March 27, 2023
Detection of circulating cell-free HPV DNA of 13 HPV types for patients with cervical cancer as potential biomarker to monitor therapy response and to detect relapse
Suzana Mittelstadt, Olga Kelemen, Jakob Admard, et al.
Orphanet Journal of Rare Diseases
|
June 25, 2026
Implementation of a medical genomics program for rare diseases in Uruguay
Camila Simoes, María Fernanda Domínguez, Soledad Rodriguez, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]
|
March 27, 2020
PET/MRI and genetic intrapatient heterogeneity in head and neck cancers
Kerstin Clasen, Sara Leibfarth, Franz J Hilke, et al.
Annals of Neurology
|
May 4, 2010
First appraisal of brain pathology owing to A30P mutant alpha-synuclein
Kay Seidel, Ludger Schöls, Silke Nuber, et al.
Page
of 32