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Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 22, 2020
TDAG51 (T-Cell Death-Associated Gene 51) Is a Key Modulator of Vascular Calcification and Osteogenic Transdifferentiation of Arterial Smooth Muscle Cells
Khrystyna Platko, Paul F Lebeau, Gabriel Gyulay, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2006
Candidate loci for Zimmermann-Laband syndrome at 3p14.3
Hyung-Goo Kim, Anne W Higgins, Steven R Herrick, et al.
JCI Insight
|
February 6, 2019
β Cell tone is defined by proglucagon peptides through cAMP signaling
Megan E Capozzi, Berit Svendsen, Sara E Encisco, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
September 27, 2022
IgG Subclass-Dependent Pulmonary Antigen Retention during Acute IgG-Dependent Systemic Anaphylaxis in Mice
Biliana Todorova, Ophélie Godon, Eva Conde, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
March 14, 2012
Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients
Eliana Marisa Ramos, Pamela Keagle, Tammy Gillis, et al.
Cell Metabolism
|
February 21, 2017
Converting Adult Pancreatic Islet α Cells into β Cells by Targeting Both Dnmt1 and Arx
Harini Chakravarthy, Xueying Gu, Martin Enge, et al.
Human Molecular Genetics
|
March 4, 2000
Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice
V C Wheeler, J K White, C A Gutekunst, et al.
The Journal of Infectious Diseases
|
July 3, 2020
Attribution of Pediatric Acute Gastroenteritis Episodes and Emergency Department Visits to Norovirus Genogroups I and II
Gillian A M Tarr, Xiao-Li Pang, Ran Zhuo, et al.
Scientific Reports
|
February 12, 2016
Metabolic disruption identified in the Huntington's disease transgenic sheep model
Renee R Handley, Suzanne J Reid, Stefano Patassini, et al.
Human Mutation
|
April 4, 2003
Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis
Carla A Teixeira, Janice Espinola, Liang Huo, et al.
Page
of 131
Search research articles
Search
Showing results (981-990 of 1,304) with videos related to
Sort By:
Page
of 131
Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 22, 2020
TDAG51 (T-Cell Death-Associated Gene 51) Is a Key Modulator of Vascular Calcification and Osteogenic Transdifferentiation of Arterial Smooth Muscle Cells
Khrystyna Platko, Paul F Lebeau, Gabriel Gyulay, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2006
Candidate loci for Zimmermann-Laband syndrome at 3p14.3
Hyung-Goo Kim, Anne W Higgins, Steven R Herrick, et al.
JCI Insight
|
February 6, 2019
β Cell tone is defined by proglucagon peptides through cAMP signaling
Megan E Capozzi, Berit Svendsen, Sara E Encisco, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
September 27, 2022
IgG Subclass-Dependent Pulmonary Antigen Retention during Acute IgG-Dependent Systemic Anaphylaxis in Mice
Biliana Todorova, Ophélie Godon, Eva Conde, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
March 14, 2012
Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients
Eliana Marisa Ramos, Pamela Keagle, Tammy Gillis, et al.
Cell Metabolism
|
February 21, 2017
Converting Adult Pancreatic Islet α Cells into β Cells by Targeting Both Dnmt1 and Arx
Harini Chakravarthy, Xueying Gu, Martin Enge, et al.
Human Molecular Genetics
|
March 4, 2000
Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice
V C Wheeler, J K White, C A Gutekunst, et al.
The Journal of Infectious Diseases
|
July 3, 2020
Attribution of Pediatric Acute Gastroenteritis Episodes and Emergency Department Visits to Norovirus Genogroups I and II
Gillian A M Tarr, Xiao-Li Pang, Ran Zhuo, et al.
Scientific Reports
|
February 12, 2016
Metabolic disruption identified in the Huntington's disease transgenic sheep model
Renee R Handley, Suzanne J Reid, Stefano Patassini, et al.
Human Mutation
|
April 4, 2003
Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis
Carla A Teixeira, Janice Espinola, Liang Huo, et al.
Page
of 131