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J Probst

Showing results (261-270 of 283) with videos related to

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Orphanet Journal of Rare Diseases|June 14, 2015
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformationsF J Probst, R A James, L C Burrage, et al.
Cytokine|January 28, 2021
Aerobic exercise ameliorates survival, clinical score, lung inflammation, DNA and protein damage in septic miceAlice H S Sumar, Ariany M Vieira, Gisele H C Martins, et al.
Nature Communications|November 27, 2014
Biology of a widespread uncultivated archaeon that contributes to carbon fixation in the subsurfaceAlexander J Probst, Thomas Weinmaier, Kasie Raymann, et al.
Plos Genetics|March 29, 2014
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndromeMichael F Wangler, Claudia Gonzaga-Jauregui, Tomasz Gambin, et al.
Astrobiology|October 3, 2025
Planning Considerations Related to Contamination Control for the Return and Analysis of Martian SamplesAlex L Sessions, Cara Magnabosco, Hazel A Barton, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
Science Advances|December 18, 2024
A global comparison of surface and subsurface microbiomes reveals large-scale biodiversity gradients, and a marine-terrestrial divideS Emil Ruff, Isabella Hrabe de Angelis, Megan Mullis, et al.
Water Research|December 26, 2024
Earth's most needed uncultivated aquatic prokaryotesSophie A Simon, Vera Aschmann, Annika Behrendt, et al.
Microorganisms|June 2, 2021
Microbial Hotspots in Lithic Microhabitats Inferred from DNA Fractionation and Metagenomics in the Atacama DesertDirk Schulze-Makuch, Daniel Lipus, Felix L Arens, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Pageof 29

Showing results (261-270 of 283) with videos related to

Sort By:
Pageof 29
Orphanet Journal of Rare Diseases|June 14, 2015
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformationsF J Probst, R A James, L C Burrage, et al.
Cytokine|January 28, 2021
Aerobic exercise ameliorates survival, clinical score, lung inflammation, DNA and protein damage in septic miceAlice H S Sumar, Ariany M Vieira, Gisele H C Martins, et al.
Nature Communications|November 27, 2014
Biology of a widespread uncultivated archaeon that contributes to carbon fixation in the subsurfaceAlexander J Probst, Thomas Weinmaier, Kasie Raymann, et al.
Plos Genetics|March 29, 2014
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndromeMichael F Wangler, Claudia Gonzaga-Jauregui, Tomasz Gambin, et al.
Astrobiology|October 3, 2025
Planning Considerations Related to Contamination Control for the Return and Analysis of Martian SamplesAlex L Sessions, Cara Magnabosco, Hazel A Barton, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
Science Advances|December 18, 2024
A global comparison of surface and subsurface microbiomes reveals large-scale biodiversity gradients, and a marine-terrestrial divideS Emil Ruff, Isabella Hrabe de Angelis, Megan Mullis, et al.
Water Research|December 26, 2024
Earth's most needed uncultivated aquatic prokaryotesSophie A Simon, Vera Aschmann, Annika Behrendt, et al.
Microorganisms|June 2, 2021
Microbial Hotspots in Lithic Microhabitats Inferred from DNA Fractionation and Metagenomics in the Atacama DesertDirk Schulze-Makuch, Daniel Lipus, Felix L Arens, et al.
Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Pageof 29