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Showing results (21-30 of 29) with videos related to

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Annals of Neurology|August 27, 2025
TARDBP (TDP-43) Knock-in Zebrafish Display a Late-Onset Motor Phenotype and Loss of Large Spinal Cord Motor NeuronsZiyaan A Harji, Christian J Rampal, Esteban C Rodríguez, et al.
Development (Cambridge, England)|October 17, 2024
Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesisMingqin Wang, Sen Zhao, Chenjun Shi, et al.
Journal of Medical Genetics|February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduriaJosé-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
Cellular and Molecular Life Sciences : CMLS|June 22, 2026
Targeting glucagon signaling in metabolic disorders, functional insights from zebrafish receptor knockoutsAshraf Al Madhoun, Md Zubbair Malik, Shaima Al-Beloushi, et al.
JCI Insight|December 5, 2017
Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosisShunmoogum A Patten, Dina Aggad, Jose Martinez, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Ultra-rare biallelic <i>THAP12</i> variants cause loss of function and underlie severe epileptic encephalopathyKatarzyna Ochenkowska, Bryce Rampal, Antoine Légaré, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
The Journal of Clinical Investigation|February 3, 2015
Functional variants of POC5 identified in patients with idiopathic scoliosisShunmoogum A Patten, Patricia Margaritte-Jeannin, Jean-Claude Bernard, et al.
Genome Medicine|May 12, 2026
Unprocessed U1 snRNAs as a biomarker of INTS11- and BRAT1-related neurodevelopmental disordersBeatrice Valtorta, Zuzana Polackova, Reza Maroofian, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Annals of Neurology|August 27, 2025
TARDBP (TDP-43) Knock-in Zebrafish Display a Late-Onset Motor Phenotype and Loss of Large Spinal Cord Motor NeuronsZiyaan A Harji, Christian J Rampal, Esteban C Rodríguez, et al.
Development (Cambridge, England)|October 17, 2024
Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesisMingqin Wang, Sen Zhao, Chenjun Shi, et al.
Journal of Medical Genetics|February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduriaJosé-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
Cellular and Molecular Life Sciences : CMLS|June 22, 2026
Targeting glucagon signaling in metabolic disorders, functional insights from zebrafish receptor knockoutsAshraf Al Madhoun, Md Zubbair Malik, Shaima Al-Beloushi, et al.
JCI Insight|December 5, 2017
Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosisShunmoogum A Patten, Dina Aggad, Jose Martinez, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Ultra-rare biallelic <i>THAP12</i> variants cause loss of function and underlie severe epileptic encephalopathyKatarzyna Ochenkowska, Bryce Rampal, Antoine Légaré, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
The Journal of Clinical Investigation|February 3, 2015
Functional variants of POC5 identified in patients with idiopathic scoliosisShunmoogum A Patten, Patricia Margaritte-Jeannin, Jean-Claude Bernard, et al.
Genome Medicine|May 12, 2026
Unprocessed U1 snRNAs as a biomarker of INTS11- and BRAT1-related neurodevelopmental disordersBeatrice Valtorta, Zuzana Polackova, Reza Maroofian, et al.
Pageof 3