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

Gail E Herman

Showing results (1-10 of 46) with videos related to

Pageof 5
Sort By:
ILAR Journal|March 28, 2002
Mouse models of human disease: lessons learned and promises to comeGail E Herman
Human Molecular Genetics|April 2, 2003
Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromesGail E Herman
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 9, 2012
Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndromeGail E Herman, Lisa Kratz
Human Molecular Genetics|September 25, 2003
NSDHL, an enzyme involved in cholesterol biosynthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid dropletsHugo Caldas, Gail E Herman
Human Molecular Genetics|October 10, 2006
Analysis of Nsdhl-deficient embryos reveals a role for Hedgehog signaling in early placental developmentFenglei Jiang, Gail E Herman
Journal of Lipid Research|October 9, 2010
Malformation syndromes caused by disorders of cholesterol synthesisForbes D Porter, Gail E Herman
Seminars in Pediatric Neurology|July 3, 2018
Language Regression in an Atypical SLC6A1 MutationMonica P Islam, Gail E Herman, Emily C de Los Reyes
Autism Research : Official Journal of the International Society for Autism Research|April 23, 2014
Family-based clinical associations and functional characterization of the serotonin 2A receptor gene (HTR2A) in autism spectrum disorderRyan M Smith, Wesley Banks, Emily Hansen, et al.
Journal of Lipid Research|April 5, 2005
Changes in gene expression associated with loss of function of the NSDHL sterol dehydrogenase in mouse embryonic fibroblastsDavid Cunningham, Daniel Swartzlander, Sandya Liyanarachchi, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL geneMarybeth Hummel, David Cunningham, Charles J Mullett, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
ILAR Journal|March 28, 2002
Mouse models of human disease: lessons learned and promises to comeGail E Herman
Human Molecular Genetics|April 2, 2003
Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromesGail E Herman
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 9, 2012
Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndromeGail E Herman, Lisa Kratz
Human Molecular Genetics|September 25, 2003
NSDHL, an enzyme involved in cholesterol biosynthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid dropletsHugo Caldas, Gail E Herman
Human Molecular Genetics|October 10, 2006
Analysis of Nsdhl-deficient embryos reveals a role for Hedgehog signaling in early placental developmentFenglei Jiang, Gail E Herman
Journal of Lipid Research|October 9, 2010
Malformation syndromes caused by disorders of cholesterol synthesisForbes D Porter, Gail E Herman
Seminars in Pediatric Neurology|July 3, 2018
Language Regression in an Atypical SLC6A1 MutationMonica P Islam, Gail E Herman, Emily C de Los Reyes
Autism Research : Official Journal of the International Society for Autism Research|April 23, 2014
Family-based clinical associations and functional characterization of the serotonin 2A receptor gene (HTR2A) in autism spectrum disorderRyan M Smith, Wesley Banks, Emily Hansen, et al.
Journal of Lipid Research|April 5, 2005
Changes in gene expression associated with loss of function of the NSDHL sterol dehydrogenase in mouse embryonic fibroblastsDavid Cunningham, Daniel Swartzlander, Sandya Liyanarachchi, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL geneMarybeth Hummel, David Cunningham, Charles J Mullett, et al.
Pageof 5