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N Murdoch

Showing results (81-90 of 103) with videos related to

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Human Molecular Genetics|December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouseJennifer N Murdoch, Deborah J Henderson, Kit Doudney, et al.
Human Molecular Genetics|March 13, 2010
The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesisLaura L Yates, Carsten Schnatwinkel, Jennifer N Murdoch, et al.
Developmental Biology|December 9, 2009
Secreted frizzled-related protein disrupts PCP in eye lens fiber cells that have polarised primary ciliaYuki Sugiyama, Richard J W Stump, Anke Nguyen, et al.
Human Molecular Genetics|February 19, 2009
Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathwayVictoria L Patterson, Christine Damrau, Anju Paudyal, et al.
Circulation Research|June 9, 2007
Disruption of planar cell polarity signaling results in congenital heart defects and cardiomyopathy attributable to early cardiomyocyte disorganizationHelen M Phillips, Hong Jun Rhee, Jennifer N Murdoch, et al.
Biochemical and Molecular Medicine|June 1, 1996
Bioaccumulated chlorinated hydrocarbons and red/white blood cell parametersR H Dunstan, T K Roberts, M Donohoe, et al.
Nature Genetics|November 6, 2001
Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activatorS D Bamforth, J Bragança, J J Eloranta, et al.
BMC Developmental Biology|August 14, 2010
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the earAnju Paudyal, Christine Damrau, Victoria L Patterson, et al.
Developmental Biology|July 10, 2012
The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of DishevelledDerrick M Glasco, Vinoth Sittaramane, Whitney Bryant, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 16, 2010
Atypical cadherins Celsr1-3 differentially regulate migration of facial branchiomotor neurons in miceYibo Qu, Derrick M Glasco, Libing Zhou, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouseJennifer N Murdoch, Deborah J Henderson, Kit Doudney, et al.
Human Molecular Genetics|March 13, 2010
The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesisLaura L Yates, Carsten Schnatwinkel, Jennifer N Murdoch, et al.
Developmental Biology|December 9, 2009
Secreted frizzled-related protein disrupts PCP in eye lens fiber cells that have polarised primary ciliaYuki Sugiyama, Richard J W Stump, Anke Nguyen, et al.
Human Molecular Genetics|February 19, 2009
Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathwayVictoria L Patterson, Christine Damrau, Anju Paudyal, et al.
Circulation Research|June 9, 2007
Disruption of planar cell polarity signaling results in congenital heart defects and cardiomyopathy attributable to early cardiomyocyte disorganizationHelen M Phillips, Hong Jun Rhee, Jennifer N Murdoch, et al.
Biochemical and Molecular Medicine|June 1, 1996
Bioaccumulated chlorinated hydrocarbons and red/white blood cell parametersR H Dunstan, T K Roberts, M Donohoe, et al.
Nature Genetics|November 6, 2001
Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activatorS D Bamforth, J Bragança, J J Eloranta, et al.
BMC Developmental Biology|August 14, 2010
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the earAnju Paudyal, Christine Damrau, Victoria L Patterson, et al.
Developmental Biology|July 10, 2012
The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of DishevelledDerrick M Glasco, Vinoth Sittaramane, Whitney Bryant, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 16, 2010
Atypical cadherins Celsr1-3 differentially regulate migration of facial branchiomotor neurons in miceYibo Qu, Derrick M Glasco, Libing Zhou, et al.
Pageof 11