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Bruno Reversade

Showing results (41-50 of 134) with videos related to

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Bone Reports|July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralizationCorey J Cain, Nathalie Gaborit, Wint Lwin, et al.
EMBO Molecular Medicine|April 17, 2023
RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesisSamantha Wong, Yu Xuan Tan, Abigail Yi Ting Loh, et al.
Stem Cell Research|December 20, 2021
Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 systemRobin Canac, Amandine Caillaud, Bastien Cimarosti, et al.
Genome Research|March 23, 2026
Complete genetic and epigenetic architecture of D4Z4 macrosatellites in FSHD, BAMS, and reference cohorts with D4Z4End2EndLucinda C Xiao, Ayush Semwal, Brianna St John, et al.
American Journal of Human Genetics|December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signalingJing Tian, Ling Ling, Mohammad Shboul, et al.
Cardiovascular Research|April 4, 2017
ELABELA-APJ axis protects from pressure overload heart failure and angiotensin II-induced cardiac damageTeruki Sato, Chitose Sato, Ayumi Kadowaki, et al.
Scientific Reports|January 13, 2017
Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamicsMingyue Jin, Oz Pomp, Tomoyasu Shinoda, et al.
BMC Biology|November 10, 2023
Deep transcriptome profiling reveals limited conservation of A-to-I RNA editing in XenopusTram Anh Nguyen, Jia Wei Joel Heng, Yan Ting Ng, et al.
Biomedicines|July 2, 2021
AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia SyndromeCamille Laberthonnière, Elva Maria Novoa-Del-Toro, Raphaël Chevalier, et al.
Nature Communications|March 20, 2026
IVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathyFang Yuan, Ye Sing Tan, Haofei Wang, et al.
Pageof 14

Showing results (41-50 of 134) with videos related to

Sort By:
Pageof 14
Bone Reports|July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralizationCorey J Cain, Nathalie Gaborit, Wint Lwin, et al.
EMBO Molecular Medicine|April 17, 2023
RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesisSamantha Wong, Yu Xuan Tan, Abigail Yi Ting Loh, et al.
Stem Cell Research|December 20, 2021
Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 systemRobin Canac, Amandine Caillaud, Bastien Cimarosti, et al.
Genome Research|March 23, 2026
Complete genetic and epigenetic architecture of D4Z4 macrosatellites in FSHD, BAMS, and reference cohorts with D4Z4End2EndLucinda C Xiao, Ayush Semwal, Brianna St John, et al.
American Journal of Human Genetics|December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signalingJing Tian, Ling Ling, Mohammad Shboul, et al.
Cardiovascular Research|April 4, 2017
ELABELA-APJ axis protects from pressure overload heart failure and angiotensin II-induced cardiac damageTeruki Sato, Chitose Sato, Ayumi Kadowaki, et al.
Scientific Reports|January 13, 2017
Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamicsMingyue Jin, Oz Pomp, Tomoyasu Shinoda, et al.
BMC Biology|November 10, 2023
Deep transcriptome profiling reveals limited conservation of A-to-I RNA editing in XenopusTram Anh Nguyen, Jia Wei Joel Heng, Yan Ting Ng, et al.
Biomedicines|July 2, 2021
AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia SyndromeCamille Laberthonnière, Elva Maria Novoa-Del-Toro, Raphaël Chevalier, et al.
Nature Communications|March 20, 2026
IVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathyFang Yuan, Ye Sing Tan, Haofei Wang, et al.
Pageof 14