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

A Ballabio

Showing results (71-80 of 200) with videos related to

Pageof 20
Sort By:
Human Molecular Genetics|March 1, 1995
Cloning of a human homologue of the Xenopus laevis APX gene from the ocular albinism type 1 critical regionM V Schiaffino, M T Bassi, E I Rugarli, et al.
Human Genetics|March 1, 1986
X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosomeA Ballabio, G Parenti, P Tippett, et al.
American Journal of Human Genetics|January 23, 1999
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.
Human Genetics|December 1, 1987
Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndromeA Ballabio, G Sebastio, R Carrozzo, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|October 19, 1999
Sequencing analysis of forty-eight human image cDNA clones similar to Drosophila mutant proteinS Volorio, G Simon, M Repetto, et al.
American Journal of Human Genetics|April 1, 1996
The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28A Auricchio, V Brancolini, G Casari, et al.
Nature Genetics|August 1, 1992
Kallmann syndrome due to a translocation resulting in an X/Y fusion geneS Guioli, B Incerti, E Zanaria, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
The ocular albinism type 1 gene product is a membrane glycoprotein localized to melanosomesM V Schiaffino, C Baschirotto, G Pellegrini, et al.
Human Molecular Genetics|November 18, 1998
The embryonic expression pattern of 40 murine cDNAs homologous to Drosophila mutant genes (Dres): a comparative and topographic approach to predict gene functionA Bulfone, C Gattuso, A Marchitiello, et al.
Archives of Surgery (Chicago, Ill. : 1960)|February 1, 1991
Effects of high-dose IgG on survival of surgical patients with sepsis scores of 20 or greaterL Dominioni, R Dionigi, M Zanello, et al.
Pageof 20

Showing results (71-80 of 200) with videos related to

Sort By:
Pageof 20
Human Molecular Genetics|March 1, 1995
Cloning of a human homologue of the Xenopus laevis APX gene from the ocular albinism type 1 critical regionM V Schiaffino, M T Bassi, E I Rugarli, et al.
Human Genetics|March 1, 1986
X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosomeA Ballabio, G Parenti, P Tippett, et al.
American Journal of Human Genetics|January 23, 1999
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.
Human Genetics|December 1, 1987
Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndromeA Ballabio, G Sebastio, R Carrozzo, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|October 19, 1999
Sequencing analysis of forty-eight human image cDNA clones similar to Drosophila mutant proteinS Volorio, G Simon, M Repetto, et al.
American Journal of Human Genetics|April 1, 1996
The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28A Auricchio, V Brancolini, G Casari, et al.
Nature Genetics|August 1, 1992
Kallmann syndrome due to a translocation resulting in an X/Y fusion geneS Guioli, B Incerti, E Zanaria, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
The ocular albinism type 1 gene product is a membrane glycoprotein localized to melanosomesM V Schiaffino, C Baschirotto, G Pellegrini, et al.
Human Molecular Genetics|November 18, 1998
The embryonic expression pattern of 40 murine cDNAs homologous to Drosophila mutant genes (Dres): a comparative and topographic approach to predict gene functionA Bulfone, C Gattuso, A Marchitiello, et al.
Archives of Surgery (Chicago, Ill. : 1960)|February 1, 1991
Effects of high-dose IgG on survival of surgical patients with sepsis scores of 20 or greaterL Dominioni, R Dionigi, M Zanello, et al.
Pageof 20