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Showing results (1081-1090 of 1,116) with videos related to

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Nature|April 28, 2022
TLR7 gain-of-function genetic variation causes human lupusGrant 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 disordersKevin Hilbert, Joscha Böhnlein, Charlotte Meinke, et al.
The Lancet. Planetary Health|November 6, 2025
Bundling measures for food systems transformation: a global, multimodel assessmentMarina Sundiang, Thais Diniz Oliveira, Daniel Mason-D'Croz, et al.
Nature|July 15, 2026
Food systems transformation would reshape global agricultureMatthew Gibson, Marina Sundiang, Daniel Mason-D'Croz, et al.
Nature Communications|March 3, 2019
State-of-the-art global models underestimate impacts from climate extremesJacob 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 SyndromesTamar Harel, Wan Hee Yoon, Caterina Garone, et al.
Nature Cell Biology|February 29, 2024
A guideline on the molecular ecosystem regulating ferroptosisEnyong 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 strokeGilsoon 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 MutationsSeema 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 disorderBobby G Ng, Erik A Eklund, Jill A Rosenfeld, et al.
Pageof 112

Showing results (1081-1090 of 1,116) with videos related to

Sort By:
Pageof 112
Nature|April 28, 2022
TLR7 gain-of-function genetic variation causes human lupusGrant 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 disordersKevin Hilbert, Joscha Böhnlein, Charlotte Meinke, et al.
The Lancet. Planetary Health|November 6, 2025
Bundling measures for food systems transformation: a global, multimodel assessmentMarina Sundiang, Thais Diniz Oliveira, Daniel Mason-D'Croz, et al.
Nature|July 15, 2026
Food systems transformation would reshape global agricultureMatthew Gibson, Marina Sundiang, Daniel Mason-D'Croz, et al.
Nature Communications|March 3, 2019
State-of-the-art global models underestimate impacts from climate extremesJacob 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 SyndromesTamar Harel, Wan Hee Yoon, Caterina Garone, et al.
Nature Cell Biology|February 29, 2024
A guideline on the molecular ecosystem regulating ferroptosisEnyong 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 strokeGilsoon 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 MutationsSeema 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 disorderBobby G Ng, Erik A Eklund, Jill A Rosenfeld, et al.
Pageof 112