Search research articles
Contact Us
Filters
Showing results (81-90 of 103) with videos related to
Page
of 11
Sort By:
Human Molecular Genetics
|
December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse
Jennifer 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 morphogenesis
Laura 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 cilia
Yuki 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 pathway
Victoria 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 disorganization
Helen 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 parameters
R 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-activator
S 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 ear
Anju 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 Dishevelled
Derrick 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 mice
Yibo Qu, Derrick M Glasco, Libing Zhou, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 103) with videos related to
Sort By:
Page
of 11
Human Molecular Genetics
|
December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse
Jennifer 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 morphogenesis
Laura 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 cilia
Yuki 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 pathway
Victoria 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 disorganization
Helen 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 parameters
R 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-activator
S 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 ear
Anju 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 Dishevelled
Derrick 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 mice
Yibo Qu, Derrick M Glasco, Libing Zhou, et al.
Page
of 11