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Bone Reports
|
July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization
Corey 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 embryogenesis
Samantha 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 system
Robin 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 D4Z4End2End
Lucinda 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 signaling
Jing 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 damage
Teruki Sato, Chitose Sato, Ayumi Kadowaki, et al.
Scientific Reports
|
January 13, 2017
Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamics
Mingyue 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 Xenopus
Tram 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 Syndrome
Camille Laberthonnière, Elva Maria Novoa-Del-Toro, Raphaël Chevalier, et al.
Nature Communications
|
March 20, 2026
IVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathy
Fang Yuan, Ye Sing Tan, Haofei Wang, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 134) with videos related to
Sort By:
Page
of 14
Bone Reports
|
July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization
Corey 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 embryogenesis
Samantha 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 system
Robin 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 D4Z4End2End
Lucinda 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 signaling
Jing 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 damage
Teruki Sato, Chitose Sato, Ayumi Kadowaki, et al.
Scientific Reports
|
January 13, 2017
Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamics
Mingyue 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 Xenopus
Tram 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 Syndrome
Camille Laberthonnière, Elva Maria Novoa-Del-Toro, Raphaël Chevalier, et al.
Nature Communications
|
March 20, 2026
IVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathy
Fang Yuan, Ye Sing Tan, Haofei Wang, et al.
Page
of 14