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

I Bach

Showing results (31-40 of 39) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 39 results.
Development (Cambridge, England)|December 16, 1998
Conserved regulation of mesenchymal gene expression by Fgf-8 in face and limb developmentA S Tucker, A Al Khamis, C A Ferguson, et al.
Journal of the National Cancer Institute|January 1, 1973
Relevance of the cytogenetic status in acute leukemia in adultsF W Gunz, B I Bach, P E Crossen, et al.
Genomics|September 1, 1990
Cloning of human hepatic nuclear factor 1 (HNF1) and chromosomal localization of its gene in man and mouseI Bach, Z Galcheva-Gargova, M G Mattei, et al.
Genomics|October 3, 2000
Functional characterization of the gene encoding RLIM, the corepressor of LIM homeodomain factorsH P Ostendorff, M Bossenz, A Mincheva, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 1995
P-Lim, a LIM homeodomain factor, is expressed during pituitary organ and cell commitment and synergizes with Pit-1I Bach, S J Rhodes, R V Pearse, et al.
Recent Progress in Hormone Research|January 1, 1996
Transcriptional control of cell phenotypes in the neuroendocrine systemM G Rosenfeld, I Bach, L Erkman, et al.
Nature Genetics|August 4, 1999
RLIM inhibits functional activity of LIM homeodomain transcription factors via recruitment of the histone deacetylase complexI Bach, C Rodriguez-Esteban, C Carrière, et al.
Human Molecular Genetics|May 1, 1992
An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1qF P Cremers, C M Molloy, D J van de Pol, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Development (Cambridge, England)|December 16, 1998
Conserved regulation of mesenchymal gene expression by Fgf-8 in face and limb developmentA S Tucker, A Al Khamis, C A Ferguson, et al.
Journal of the National Cancer Institute|January 1, 1973
Relevance of the cytogenetic status in acute leukemia in adultsF W Gunz, B I Bach, P E Crossen, et al.
Genomics|September 1, 1990
Cloning of human hepatic nuclear factor 1 (HNF1) and chromosomal localization of its gene in man and mouseI Bach, Z Galcheva-Gargova, M G Mattei, et al.
Genomics|October 3, 2000
Functional characterization of the gene encoding RLIM, the corepressor of LIM homeodomain factorsH P Ostendorff, M Bossenz, A Mincheva, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 1995
P-Lim, a LIM homeodomain factor, is expressed during pituitary organ and cell commitment and synergizes with Pit-1I Bach, S J Rhodes, R V Pearse, et al.
Recent Progress in Hormone Research|January 1, 1996
Transcriptional control of cell phenotypes in the neuroendocrine systemM G Rosenfeld, I Bach, L Erkman, et al.
Nature Genetics|August 4, 1999
RLIM inhibits functional activity of LIM homeodomain transcription factors via recruitment of the histone deacetylase complexI Bach, C Rodriguez-Esteban, C Carrière, et al.
Human Molecular Genetics|May 1, 1992
An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1qF P Cremers, C M Molloy, D J van de Pol, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.
Pageof 4