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Showing results (1081-1090 of 1,116) with videos related to
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Nature
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April 28, 2022
TLR7 gain-of-function genetic variation causes human lupus
Grant J Brown, Pablo F Cañete, Hao Wang, et al.
Neuroimage
|
May 26, 2024
Lack of evidence for predictive utility from resting state fMRI data for individual exposure-based cognitive behavioral therapy outcomes: A machine learning study in two large multi-site samples in anxiety disorders
Kevin Hilbert, Joscha Böhnlein, Charlotte Meinke, et al.
The Lancet. Planetary Health
|
November 6, 2025
Bundling measures for food systems transformation: a global, multimodel assessment
Marina Sundiang, Thais Diniz Oliveira, Daniel Mason-D'Croz, et al.
Nature
|
July 15, 2026
Food systems transformation would reshape global agriculture
Matthew Gibson, Marina Sundiang, Daniel Mason-D'Croz, et al.
Nature Communications
|
March 3, 2019
State-of-the-art global models underestimate impacts from climate extremes
Jacob Schewe, Simon N Gosling, Christopher Reyer, et al.
American Journal of Human Genetics
|
September 20, 2016
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes
Tamar Harel, Wan Hee Yoon, Caterina Garone, et al.
Nature Cell Biology
|
February 29, 2024
A guideline on the molecular ecosystem regulating ferroptosis
Enyong Dai, Xin Chen, Andreas Linkermann, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 22, 2024
Severe motor impairment is associated with lower contralesional brain age in chronic stroke
Gilsoon Park, Mahir H Khan, Justin W Andrushko, et al.
American Journal of Human Genetics
|
January 26, 2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations
Seema R Lalani, Pengfei Liu, Jill A Rosenfeld, et al.
Genetics in Medicine Open
|
June 5, 2025
Autosomal dominant <i>HK1</i>-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder
Bobby G Ng, Erik A Eklund, Jill A Rosenfeld, et al.
Page
of 112
Search research articles
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Showing results (1081-1090 of 1,116) with videos related to
Sort By:
Page
of 112
Nature
|
April 28, 2022
TLR7 gain-of-function genetic variation causes human lupus
Grant J Brown, Pablo F Cañete, Hao Wang, et al.
Neuroimage
|
May 26, 2024
Lack of evidence for predictive utility from resting state fMRI data for individual exposure-based cognitive behavioral therapy outcomes: A machine learning study in two large multi-site samples in anxiety disorders
Kevin Hilbert, Joscha Böhnlein, Charlotte Meinke, et al.
The Lancet. Planetary Health
|
November 6, 2025
Bundling measures for food systems transformation: a global, multimodel assessment
Marina Sundiang, Thais Diniz Oliveira, Daniel Mason-D'Croz, et al.
Nature
|
July 15, 2026
Food systems transformation would reshape global agriculture
Matthew Gibson, Marina Sundiang, Daniel Mason-D'Croz, et al.
Nature Communications
|
March 3, 2019
State-of-the-art global models underestimate impacts from climate extremes
Jacob Schewe, Simon N Gosling, Christopher Reyer, et al.
American Journal of Human Genetics
|
September 20, 2016
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes
Tamar Harel, Wan Hee Yoon, Caterina Garone, et al.
Nature Cell Biology
|
February 29, 2024
A guideline on the molecular ecosystem regulating ferroptosis
Enyong Dai, Xin Chen, Andreas Linkermann, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 22, 2024
Severe motor impairment is associated with lower contralesional brain age in chronic stroke
Gilsoon Park, Mahir H Khan, Justin W Andrushko, et al.
American Journal of Human Genetics
|
January 26, 2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations
Seema R Lalani, Pengfei Liu, Jill A Rosenfeld, et al.
Genetics in Medicine Open
|
June 5, 2025
Autosomal dominant <i>HK1</i>-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder
Bobby G Ng, Erik A Eklund, Jill A Rosenfeld, et al.
Page
of 112