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Irene E Zohn

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

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Frontiers in Cell and Developmental Biology|October 24, 2022
Parental obesity-induced changes in developmental programmingLaura R Cechinel, Rachael A Batabyal, Robert J Freishtat, et al.
Annual Review of Neuroscience|February 27, 2020
Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental PathologyThomas M Maynard, Irene E Zohn, Sally A Moody, et al.
American Journal of Medical Genetics. Part A|October 20, 2022
ALDH1A2-related disorder: A new genetic syndrome due to alteration of the retinoic acid pathwayEyby Leon, Claris Nde, Randall S Ray, et al.
Developmental Biology|November 30, 2016
Supt20 is required for development of the axial skeletonSunita Warrier, Samer Nuwayhid, Julia A Sabatino, et al.
Development (Cambridge, England)|August 13, 2010
The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closureJinzhe Mao, David M McKean, Sunita Warrier, et al.
Cell|June 6, 2006
p38 and a p38-interacting protein are critical for downregulation of E-cadherin during mouse gastrulationIrene E Zohn, Yingqiu Li, Edward Y Skolnik, et al.
Disease Models & Mechanisms|December 21, 2013
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndromeBeverly A Karpinski, Thomas M Maynard, Matthew S Fralish, et al.
Developmental Biology|May 24, 2014
Hectd1 is required for development of the junctional zone of the placentaAnjali A Sarkar, Samer J Nuwayhid, Thomas Maynard, et al.
Developmental Biology|November 12, 2015
Hard to swallow: Developmental biological insights into pediatric dysphagiaAnthony-Samuel LaMantia, Sally A Moody, Thomas M Maynard, et al.
Blood|February 10, 2007
The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin diseaseIrene E Zohn, Ivana De Domenico, Andrew Pollock, et al.
Pageof 4

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

Sort By:
Pageof 4
Frontiers in Cell and Developmental Biology|October 24, 2022
Parental obesity-induced changes in developmental programmingLaura R Cechinel, Rachael A Batabyal, Robert J Freishtat, et al.
Annual Review of Neuroscience|February 27, 2020
Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental PathologyThomas M Maynard, Irene E Zohn, Sally A Moody, et al.
American Journal of Medical Genetics. Part A|October 20, 2022
ALDH1A2-related disorder: A new genetic syndrome due to alteration of the retinoic acid pathwayEyby Leon, Claris Nde, Randall S Ray, et al.
Developmental Biology|November 30, 2016
Supt20 is required for development of the axial skeletonSunita Warrier, Samer Nuwayhid, Julia A Sabatino, et al.
Development (Cambridge, England)|August 13, 2010
The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closureJinzhe Mao, David M McKean, Sunita Warrier, et al.
Cell|June 6, 2006
p38 and a p38-interacting protein are critical for downregulation of E-cadherin during mouse gastrulationIrene E Zohn, Yingqiu Li, Edward Y Skolnik, et al.
Disease Models & Mechanisms|December 21, 2013
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndromeBeverly A Karpinski, Thomas M Maynard, Matthew S Fralish, et al.
Developmental Biology|May 24, 2014
Hectd1 is required for development of the junctional zone of the placentaAnjali A Sarkar, Samer J Nuwayhid, Thomas Maynard, et al.
Developmental Biology|November 12, 2015
Hard to swallow: Developmental biological insights into pediatric dysphagiaAnthony-Samuel LaMantia, Sally A Moody, Thomas M Maynard, et al.
Blood|February 10, 2007
The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin diseaseIrene E Zohn, Ivana De Domenico, Andrew Pollock, et al.
Pageof 4