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

Janna Nousbeck

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
Experimental Dermatology|November 17, 2021
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasisLiat Samuelov, Ron Bochner, Lee Magal, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1Ofer Sarig, Dorit Goldsher, Janna Nousbeck, et al.
American Journal of Human Genetics|June 19, 2012
Familial pityriasis rubra pilaris is caused by mutations in CARD14Dana Fuchs-Telem, Ofer Sarig, Maurice A M van Steensel, et al.
American Journal of Human Genetics|July 31, 2012
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutationOfer Sarig, Sagi Nahum, Debora Rapaport, et al.
American Journal of Human Genetics|April 29, 2008
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesisJanna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, et al.
Experimental Dermatology|May 6, 2015
RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63Emily Warshauer, Liat Samuelov, Ofer Sarig, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
Experimental Dermatology|November 17, 2021
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasisLiat Samuelov, Ron Bochner, Lee Magal, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1Ofer Sarig, Dorit Goldsher, Janna Nousbeck, et al.
American Journal of Human Genetics|June 19, 2012
Familial pityriasis rubra pilaris is caused by mutations in CARD14Dana Fuchs-Telem, Ofer Sarig, Maurice A M van Steensel, et al.
American Journal of Human Genetics|July 31, 2012
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutationOfer Sarig, Sagi Nahum, Debora Rapaport, et al.
American Journal of Human Genetics|April 29, 2008
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesisJanna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, et al.
Experimental Dermatology|May 6, 2015
RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63Emily Warshauer, Liat Samuelov, Ofer Sarig, et al.
Pageof 2