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Phillip Grote

Showing results (31-40 of 38) with videos related to

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Journal of Medical Genetics|November 15, 2022
X-linked variations in <i>SHROOM4</i> are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systemsCaroline M Kolvenbach, Tim Felger, Luca Schierbaum, et al.
Nature Communications|April 3, 2023
Retinoic acid signaling modulation guides in vitro specification of human heart field-specific progenitor poolsDorota Zawada, Jessica Kornherr, Anna B Meier, et al.
Nature|February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulatorLila Allou, Sara Balzano, Andreas Magg, et al.
American Journal of Human Genetics|May 4, 2019
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract ObstructionCaroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, et al.
Plos One|June 6, 2020
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresiaRong Zhang, Jan Gehlen, Amit Kawalia, et al.
Frontiers in Cell and Developmental Biology|August 28, 2020
<i>SLC20A1</i> Is Involved in Urinary Tract and Urorectal DevelopmentJohanna Magdalena Rieke, Rong Zhang, Doreen Braun, et al.
NPJ Genomic Medicine|March 1, 2024
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomaliesJil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Journal of Medical Genetics|November 15, 2022
X-linked variations in <i>SHROOM4</i> are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systemsCaroline M Kolvenbach, Tim Felger, Luca Schierbaum, et al.
Nature Communications|April 3, 2023
Retinoic acid signaling modulation guides in vitro specification of human heart field-specific progenitor poolsDorota Zawada, Jessica Kornherr, Anna B Meier, et al.
Nature|February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulatorLila Allou, Sara Balzano, Andreas Magg, et al.
American Journal of Human Genetics|May 4, 2019
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract ObstructionCaroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, et al.
Plos One|June 6, 2020
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresiaRong Zhang, Jan Gehlen, Amit Kawalia, et al.
Frontiers in Cell and Developmental Biology|August 28, 2020
<i>SLC20A1</i> Is Involved in Urinary Tract and Urorectal DevelopmentJohanna Magdalena Rieke, Rong Zhang, Doreen Braun, et al.
NPJ Genomic Medicine|March 1, 2024
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomaliesJil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
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