Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Sally H Cross

Showing results (1-10 of 23) with videos related to

Pageof 3
Sort By:
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 13, 2002
Identification and characterization of a novel murine beta-defensin-related geneGillian M Morrison, Mark Rolfe, Fiona M Kilanowski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 1, 2012
Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylationGewei Lian, Jie Lu, Jianjun Hu, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Genotype-phenotype correlation of mouse pde6b mutationsAlan W Hart, Lisa McKie, Joanne E Morgan, et al.
Journal of Cell Science|September 4, 2008
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentTom R Webb, Sally H Cross, Lisa McKie, et al.
Nature|April 25, 2003
The methylated component of the Neurospora crassa genomeEric U Selker, Nikolaos A Tountas, Sally H Cross, et al.
Human Molecular Genetics|July 11, 2006
Cardiac malformations and midline skeletal defects in mice lacking filamin AAlan W Hart, Joanne E Morgan, Jürgen Schneider, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 16, 2004
Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptorDaekee Lee, Sally H Cross, Karen E Strunk, et al.
Human Molecular Genetics|October 15, 2010
The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotypeSally H Cross, Lisa McKie, Katrine West, et al.
BMC Research Notes|February 29, 2012
Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseasesPanagiotis Douvaras, Weijia Liu, Richard L Mort, et al.
Scientific Reports|January 18, 2020
Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal functionAmy S Findlay, Lisa McKie, Margaret Keighren, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 13, 2002
Identification and characterization of a novel murine beta-defensin-related geneGillian M Morrison, Mark Rolfe, Fiona M Kilanowski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 1, 2012
Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylationGewei Lian, Jie Lu, Jianjun Hu, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Genotype-phenotype correlation of mouse pde6b mutationsAlan W Hart, Lisa McKie, Joanne E Morgan, et al.
Journal of Cell Science|September 4, 2008
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentTom R Webb, Sally H Cross, Lisa McKie, et al.
Nature|April 25, 2003
The methylated component of the Neurospora crassa genomeEric U Selker, Nikolaos A Tountas, Sally H Cross, et al.
Human Molecular Genetics|July 11, 2006
Cardiac malformations and midline skeletal defects in mice lacking filamin AAlan W Hart, Joanne E Morgan, Jürgen Schneider, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 16, 2004
Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptorDaekee Lee, Sally H Cross, Karen E Strunk, et al.
Human Molecular Genetics|October 15, 2010
The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotypeSally H Cross, Lisa McKie, Katrine West, et al.
BMC Research Notes|February 29, 2012
Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseasesPanagiotis Douvaras, Weijia Liu, Richard L Mort, et al.
Scientific Reports|January 18, 2020
Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal functionAmy S Findlay, Lisa McKie, Margaret Keighren, et al.
Pageof 3