Search research articles
Contact Us
Filters
Showing results (121-130 of 141) with videos related to
Page
of 15
Sort By:
Biomedicines
|
April 23, 2022
Longitudinal [<sup>18</sup>F]GE-180 PET Imaging Facilitates In Vivo Monitoring of TSPO Expression in the GL261 Glioblastoma Mouse Model
Adrien Holzgreve, Dennis Pötter, Matthias Brendel, et al.
NPJ Genomic Medicine
|
September 6, 2022
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1
Sergey V Lobanov, Branduff McAllister, Mia McDade-Kumar, et al.
Experimental Hematology & Oncology
|
February 15, 2017
A randomized exploratory phase 2 study in patients with chemotherapy-related peripheral neuropathy evaluating whole-body vibration training as adjunct to an integrated program including massage, passive mobilization and physical exercises
Stefan S Schönsteiner, Heidi Bauder Mißbach, Axel Benner, et al.
Human Brain Mapping
|
August 2, 2016
Natural variation in sensory-motor white matter organization influences manifestations of Huntington's disease
Michael Orth, Sarah Gregory, Rachael I Scahill, et al.
Cancer Letters
|
November 22, 2016
Genomic amplification of Fanconi anemia complementation group A (FancA) in head and neck squamous cell carcinoma (HNSCC): Cellular mechanisms of radioresistance and clinical relevance
Julia Hess, Kristian Unger, Michael Orth, et al.
Plos Genetics
|
May 12, 2018
Population-specific genetic modification of Huntington's disease in Venezuela
Michael J Chao, Kyung-Hee Kim, Jun Wan Shin, et al.
American Journal of Human Genetics
|
June 27, 2020
Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects
Kyung-Hee Kim, Eun Pyo Hong, Jun Wan Shin, et al.
Biomed Research International
|
December 8, 2017
Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer
Pedro Sernadela, Lorena González-Castro, Claudio Carta, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 12, 2024
Posttranscriptional regulation of <i>FAN1</i> by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease
Kyung-Hee Kim, Eun Pyo Hong, Yukyeong Lee, et al.
Human Molecular Genetics
|
January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
Sarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 141) with videos related to
Sort By:
Page
of 15
Biomedicines
|
April 23, 2022
Longitudinal [<sup>18</sup>F]GE-180 PET Imaging Facilitates In Vivo Monitoring of TSPO Expression in the GL261 Glioblastoma Mouse Model
Adrien Holzgreve, Dennis Pötter, Matthias Brendel, et al.
NPJ Genomic Medicine
|
September 6, 2022
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1
Sergey V Lobanov, Branduff McAllister, Mia McDade-Kumar, et al.
Experimental Hematology & Oncology
|
February 15, 2017
A randomized exploratory phase 2 study in patients with chemotherapy-related peripheral neuropathy evaluating whole-body vibration training as adjunct to an integrated program including massage, passive mobilization and physical exercises
Stefan S Schönsteiner, Heidi Bauder Mißbach, Axel Benner, et al.
Human Brain Mapping
|
August 2, 2016
Natural variation in sensory-motor white matter organization influences manifestations of Huntington's disease
Michael Orth, Sarah Gregory, Rachael I Scahill, et al.
Cancer Letters
|
November 22, 2016
Genomic amplification of Fanconi anemia complementation group A (FancA) in head and neck squamous cell carcinoma (HNSCC): Cellular mechanisms of radioresistance and clinical relevance
Julia Hess, Kristian Unger, Michael Orth, et al.
Plos Genetics
|
May 12, 2018
Population-specific genetic modification of Huntington's disease in Venezuela
Michael J Chao, Kyung-Hee Kim, Jun Wan Shin, et al.
American Journal of Human Genetics
|
June 27, 2020
Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects
Kyung-Hee Kim, Eun Pyo Hong, Jun Wan Shin, et al.
Biomed Research International
|
December 8, 2017
Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer
Pedro Sernadela, Lorena González-Castro, Claudio Carta, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 12, 2024
Posttranscriptional regulation of <i>FAN1</i> by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease
Kyung-Hee Kim, Eun Pyo Hong, Yukyeong Lee, et al.
Human Molecular Genetics
|
January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
Sarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Page
of 15