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Showing results (1041-1050 of 1,304) with videos related to
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Diabetes
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October 15, 2011
Islet cholesterol accumulation due to loss of ABCA1 leads to impaired exocytosis of insulin granules
Janine K Kruit, Nadeeja Wijesekara, Jocelyn E Manning Fox, et al.
Genes & Development
|
July 4, 2020
A role for alternative splicing in circadian control of exocytosis and glucose homeostasis
Biliana Marcheva, Mark Perelis, Benjamin J Weidemann, et al.
Cell Metabolism
|
June 8, 2017
N-acyl Taurines and Acylcarnitines Cause an Imbalance in Insulin Synthesis and Secretion Provoking β Cell Dysfunction in Type 2 Diabetes
Michaela Aichler, Daniela Borgmann, Jan Krumsiek, et al.
Nature Communications
|
November 8, 2019
An engineered human Fc domain that behaves like a pH-toggle switch for ultra-long circulation persistence
Chang-Han Lee, Tae Hyun Kang, Ophélie Godon, et al.
Science Translational Medicine
|
February 14, 2020
GLP-1 receptor agonists synergize with DYRK1A inhibitors to potentiate functional human β cell regeneration
Courtney Ackeifi, Peng Wang, Esra Karakose, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1994
Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat
Christine M Ambrose, Mabel P Duyao, Glenn Barnes, et al.
Human Molecular Genetics
|
April 19, 2013
Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy
Jong-Min Lee, Ekaterina I Galkina, Rachel M Levantovsky, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 29, 2017
Humanized mouse model supports development, function, and tissue residency of human natural killer cells
Dietmar Herndler-Brandstetter, Liang Shan, Yi Yao, et al.
Human Molecular Genetics
|
January 12, 2021
Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs
Roy Jung, Yejin Lee, Douglas Barker, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2024
Identification of genetic modifiers of Huntington's disease somatic CAG repeat instability by in vivo CRISPR-Cas9 genome editing
Ricardo Mouro Pinto, Ryan Murtha, António Azevedo, et al.
Page
of 131
Search research articles
Search
Showing results (1041-1050 of 1,304) with videos related to
Sort By:
Page
of 131
Diabetes
|
October 15, 2011
Islet cholesterol accumulation due to loss of ABCA1 leads to impaired exocytosis of insulin granules
Janine K Kruit, Nadeeja Wijesekara, Jocelyn E Manning Fox, et al.
Genes & Development
|
July 4, 2020
A role for alternative splicing in circadian control of exocytosis and glucose homeostasis
Biliana Marcheva, Mark Perelis, Benjamin J Weidemann, et al.
Cell Metabolism
|
June 8, 2017
N-acyl Taurines and Acylcarnitines Cause an Imbalance in Insulin Synthesis and Secretion Provoking β Cell Dysfunction in Type 2 Diabetes
Michaela Aichler, Daniela Borgmann, Jan Krumsiek, et al.
Nature Communications
|
November 8, 2019
An engineered human Fc domain that behaves like a pH-toggle switch for ultra-long circulation persistence
Chang-Han Lee, Tae Hyun Kang, Ophélie Godon, et al.
Science Translational Medicine
|
February 14, 2020
GLP-1 receptor agonists synergize with DYRK1A inhibitors to potentiate functional human β cell regeneration
Courtney Ackeifi, Peng Wang, Esra Karakose, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1994
Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat
Christine M Ambrose, Mabel P Duyao, Glenn Barnes, et al.
Human Molecular Genetics
|
April 19, 2013
Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy
Jong-Min Lee, Ekaterina I Galkina, Rachel M Levantovsky, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 29, 2017
Humanized mouse model supports development, function, and tissue residency of human natural killer cells
Dietmar Herndler-Brandstetter, Liang Shan, Yi Yao, et al.
Human Molecular Genetics
|
January 12, 2021
Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs
Roy Jung, Yejin Lee, Douglas Barker, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2024
Identification of genetic modifiers of Huntington's disease somatic CAG repeat instability by in vivo CRISPR-Cas9 genome editing
Ricardo Mouro Pinto, Ryan Murtha, António Azevedo, et al.
Page
of 131