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Diana M Juriloff

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Birth Defects Research. Part A, Clinical and Molecular Teratology|April 3, 2008
First perspectives from the new editorDiana M Juriloff
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 9, 2008
Mouse genetic models of cleft lip with or without cleft palateDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 22, 2005
Maternal diet alters exencephaly frequency in SELH/Bc strain mouse embryosMuriel J Harris, Diana M Juriloff
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 27, 2010
An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closureMuriel J Harris, Diana M Juriloff
Journal of Developmental Biology|August 24, 2018
Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary StudiesDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 4, 2012
Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevationDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 21, 2006
Mouse mutants with neural tube closure defects and their role in understanding human neural tube defectsMuriel J Harris, Diana M Juriloff
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 2, 2012
A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defectsDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 27, 2004
A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two lociDiana M Juriloff, Muriel J Harris, Sarah L Dewell
Genomics|December 21, 2004
The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 geneDiana M Juriloff, Muriel J Harris, Diana G Mah
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 3, 2008
First perspectives from the new editorDiana M Juriloff
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 9, 2008
Mouse genetic models of cleft lip with or without cleft palateDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 22, 2005
Maternal diet alters exencephaly frequency in SELH/Bc strain mouse embryosMuriel J Harris, Diana M Juriloff
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 27, 2010
An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closureMuriel J Harris, Diana M Juriloff
Journal of Developmental Biology|August 24, 2018
Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary StudiesDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 4, 2012
Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevationDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 21, 2006
Mouse mutants with neural tube closure defects and their role in understanding human neural tube defectsMuriel J Harris, Diana M Juriloff
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 2, 2012
A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defectsDiana M Juriloff, Muriel J Harris
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 27, 2004
A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two lociDiana M Juriloff, Muriel J Harris, Sarah L Dewell
Genomics|December 21, 2004
The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 geneDiana M Juriloff, Muriel J Harris, Diana G Mah
Pageof 2