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American Journal of Medical Genetics. Part A
|
March 3, 2004
Clinical and radiographic findings in multiple epiphyseal dysplasia caused by MATN3 mutations: description of 12 patients
Outi Mäkitie, Geert R Mortier, Malwina Czarny-Ratajczak, et al.
BMC Geriatrics
|
November 17, 2021
The PREvention Program for Alzheimer's RElated Delirium (PREPARED) cluster randomized trial: a study protocol
Machelle Wilchesky, Stephanie A Ballard, Philippe Voyer, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
May 1, 2026
Functional Analysis of Ligand-Gated Chloride Channels in a Cnidarian Sheds Light on the Evolution of Inhibitory Signaling
Abhilasha Ojha, Linda Kloss, Juan D Montenegro, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 6, 2000
Cytoskeletal abnormalities in chondrocytes with EXT1 and EXT2 mutations
M A Bernard, D A Hogue, W G Cole, et al.
Cell Motility and the Cytoskeleton
|
February 13, 2001
Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes
M A Bernard, C E Hall, D A Hogue, et al.
Radiation Research
|
December 11, 2013
Acute and fractionated exposure to high-LET (56)Fe HZE-particle radiation both result in similar long-term deficits in adult hippocampal neurogenesis
Phillip D Rivera, Hung-Ying Shih, Junie A Leblanc, et al.
The Journal of Clinical Investigation
|
May 3, 2005
A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders
Robert C Gensure, Outi Mäkitie, Catherine Barclay, et al.
The New England Journal of Medicine
|
October 3, 1996
The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. Cholesterol and Recurrent Events Trial investigators
F M Sacks, M A Pfeffer, L A Moye, et al.
Infant Behavior & Development
|
July 31, 2025
Development and validation of the motor measures in the NIH Baby Toolbox®
Karen E Adolph, Whitney G Cole, Miriam A Novack, et al.
Nature Genetics
|
October 4, 2011
Mutations in TRPV4 cause an inherited arthropathy of hands and feet
Shireen R Lamandé, Yuan Yuan, Irma L Gresshoff, et al.
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Showing results (731-740 of 805) with videos related to
Sort By:
Page
of 81
American Journal of Medical Genetics. Part A
|
March 3, 2004
Clinical and radiographic findings in multiple epiphyseal dysplasia caused by MATN3 mutations: description of 12 patients
Outi Mäkitie, Geert R Mortier, Malwina Czarny-Ratajczak, et al.
BMC Geriatrics
|
November 17, 2021
The PREvention Program for Alzheimer's RElated Delirium (PREPARED) cluster randomized trial: a study protocol
Machelle Wilchesky, Stephanie A Ballard, Philippe Voyer, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
May 1, 2026
Functional Analysis of Ligand-Gated Chloride Channels in a Cnidarian Sheds Light on the Evolution of Inhibitory Signaling
Abhilasha Ojha, Linda Kloss, Juan D Montenegro, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 6, 2000
Cytoskeletal abnormalities in chondrocytes with EXT1 and EXT2 mutations
M A Bernard, D A Hogue, W G Cole, et al.
Cell Motility and the Cytoskeleton
|
February 13, 2001
Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes
M A Bernard, C E Hall, D A Hogue, et al.
Radiation Research
|
December 11, 2013
Acute and fractionated exposure to high-LET (56)Fe HZE-particle radiation both result in similar long-term deficits in adult hippocampal neurogenesis
Phillip D Rivera, Hung-Ying Shih, Junie A Leblanc, et al.
The Journal of Clinical Investigation
|
May 3, 2005
A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders
Robert C Gensure, Outi Mäkitie, Catherine Barclay, et al.
The New England Journal of Medicine
|
October 3, 1996
The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. Cholesterol and Recurrent Events Trial investigators
F M Sacks, M A Pfeffer, L A Moye, et al.
Infant Behavior & Development
|
July 31, 2025
Development and validation of the motor measures in the NIH Baby Toolbox®
Karen E Adolph, Whitney G Cole, Miriam A Novack, et al.
Nature Genetics
|
October 4, 2011
Mutations in TRPV4 cause an inherited arthropathy of hands and feet
Shireen R Lamandé, Yuan Yuan, Irma L Gresshoff, et al.
Page
of 81