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Sumantra Chatterjee

Showing results (21-30 of 35) with videos related to

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Human Molecular Genetics|February 11, 2015
Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphismsAshish Kapoor, Qian Jiang, Sumantra Chatterjee, et al.
Plos Genetics|November 10, 2023
RET enhancer haplotype-dependent remodeling of the human fetal gut development programSumantra Chatterjee, Lauren E Fries, Or Yaacov, et al.
Biotechnology Letters|August 3, 2013
A conditional mouse line for lineage tracing of Sox9 loss-of-function cells using enhanced green fluorescent proteinSumantra Chatterjee, Petra Kraus, V Sivakamasundari, et al.
Genomics Data|September 28, 2016
Genome wide binding (ChIP-Seq) of murine Bapx1 and Sox9 proteins in vivo and in vitroSumantra Chatterjee, Petra Kraus, V Sivakamasundari, et al.
Genomics Data|June 24, 2015
Gene expression profiles of <i>Bapx1</i> expressing FACS sorted cells from wildtype and <i>Bapx1-EGFP</i> null mouse embryosSumantra Chatterjee, V Sivakamasundari, Petra Kraus, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 2023
<i>Ret</i> deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system developmentElizabeth Vincent, Sumantra Chatterjee, Gabrielle H Cannon, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 25, 2015
Intestinal Neuronal Dysplasia-Like Submucosal Ganglion Cell Hyperplasia at the Proximal Margins of Hirschsprung Disease ResectionsMaya Swaminathan, Assaf P Oron, Sumantra Chatterjee, et al.
Journal of Pediatric Surgery|December 6, 2014
Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung diseaseGunadi, Ashish Kapoor, Albee Yun Ling, et al.
Cell|October 4, 2016
Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung DiseaseSumantra Chatterjee, Ashish Kapoor, Jennifer A Akiyama, et al.
BMC Genomics|December 7, 2014
In vivo genome-wide analysis of multiple tissues identifies gene regulatory networks, novel functions and downstream regulatory genes for Bapx1 and its co-regulation with Sox9 in the mammalian vertebral columnSumantra Chatterjee, V Sivakamasundari, Sook Peng Yap, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|February 11, 2015
Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphismsAshish Kapoor, Qian Jiang, Sumantra Chatterjee, et al.
Plos Genetics|November 10, 2023
RET enhancer haplotype-dependent remodeling of the human fetal gut development programSumantra Chatterjee, Lauren E Fries, Or Yaacov, et al.
Biotechnology Letters|August 3, 2013
A conditional mouse line for lineage tracing of Sox9 loss-of-function cells using enhanced green fluorescent proteinSumantra Chatterjee, Petra Kraus, V Sivakamasundari, et al.
Genomics Data|September 28, 2016
Genome wide binding (ChIP-Seq) of murine Bapx1 and Sox9 proteins in vivo and in vitroSumantra Chatterjee, Petra Kraus, V Sivakamasundari, et al.
Genomics Data|June 24, 2015
Gene expression profiles of <i>Bapx1</i> expressing FACS sorted cells from wildtype and <i>Bapx1-EGFP</i> null mouse embryosSumantra Chatterjee, V Sivakamasundari, Petra Kraus, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 2023
<i>Ret</i> deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system developmentElizabeth Vincent, Sumantra Chatterjee, Gabrielle H Cannon, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 25, 2015
Intestinal Neuronal Dysplasia-Like Submucosal Ganglion Cell Hyperplasia at the Proximal Margins of Hirschsprung Disease ResectionsMaya Swaminathan, Assaf P Oron, Sumantra Chatterjee, et al.
Journal of Pediatric Surgery|December 6, 2014
Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung diseaseGunadi, Ashish Kapoor, Albee Yun Ling, et al.
Cell|October 4, 2016
Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung DiseaseSumantra Chatterjee, Ashish Kapoor, Jennifer A Akiyama, et al.
BMC Genomics|December 7, 2014
In vivo genome-wide analysis of multiple tissues identifies gene regulatory networks, novel functions and downstream regulatory genes for Bapx1 and its co-regulation with Sox9 in the mammalian vertebral columnSumantra Chatterjee, V Sivakamasundari, Sook Peng Yap, et al.
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