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Jun Z Li

Showing results (71-80 of 107) with videos related to

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Developmental Cell|March 23, 2022
Cellular heterogeneity of human fallopian tubes in normal and hydrosalpinx disease states identified using scRNA-seqNicole D Ulrich, Yu-Chi Shen, Qianyi Ma, et al.
Methods (San Diego, Calif.)|February 14, 2006
Application of microarray technology in primate behavioral neuroscience researchAdriaan M Karssen, Jun Z Li, Song Her, et al.
Journal of Medical Genetics|May 15, 2012
Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorderJirair Krikor Bedoyan, Valerie M Schaibley, Weiping Peng, et al.
Stem Cell Reports|November 23, 2023
Deriving early single-rosette brain organoids from human pluripotent stem cellsAndrew M Tidball, Wei Niu, Qianyi Ma, et al.
Blood|May 15, 2014
Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemiaMark J Kiel, Thirunavukkarasu Velusamy, Delphine Rolland, et al.
Annals of Neurology|April 1, 2018
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defectsEunju Seong, Ryan Insolera, Marija Dulovic, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2017
Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor lociRandal J Westrick, Kärt Tomberg, Amy E Siebert, et al.
Frontiers in Genetics|January 7, 2014
G protein-linked signaling pathways in bipolar and major depressive disordersHiroaki Tomita, Mary E Ziegler, Helen B Kim, et al.
Human Genetics|November 20, 2018
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutationsDavor Lessel, Ayse Bilge Ozel, Susan E Campbell, et al.
Elife|January 27, 2016
Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delayMyungjin Kim, Erin Sandford, Damian Gatica, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
Developmental Cell|March 23, 2022
Cellular heterogeneity of human fallopian tubes in normal and hydrosalpinx disease states identified using scRNA-seqNicole D Ulrich, Yu-Chi Shen, Qianyi Ma, et al.
Methods (San Diego, Calif.)|February 14, 2006
Application of microarray technology in primate behavioral neuroscience researchAdriaan M Karssen, Jun Z Li, Song Her, et al.
Journal of Medical Genetics|May 15, 2012
Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorderJirair Krikor Bedoyan, Valerie M Schaibley, Weiping Peng, et al.
Stem Cell Reports|November 23, 2023
Deriving early single-rosette brain organoids from human pluripotent stem cellsAndrew M Tidball, Wei Niu, Qianyi Ma, et al.
Blood|May 15, 2014
Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemiaMark J Kiel, Thirunavukkarasu Velusamy, Delphine Rolland, et al.
Annals of Neurology|April 1, 2018
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defectsEunju Seong, Ryan Insolera, Marija Dulovic, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2017
Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor lociRandal J Westrick, Kärt Tomberg, Amy E Siebert, et al.
Frontiers in Genetics|January 7, 2014
G protein-linked signaling pathways in bipolar and major depressive disordersHiroaki Tomita, Mary E Ziegler, Helen B Kim, et al.
Human Genetics|November 20, 2018
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutationsDavor Lessel, Ayse Bilge Ozel, Susan E Campbell, et al.
Elife|January 27, 2016
Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delayMyungjin Kim, Erin Sandford, Damian Gatica, et al.
Pageof 11