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

H Globerman

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 13, 1998
Analysis of the insulin receptor gene tyrosine kinase domain in obese patients with hyperandrogenism, insulin resistance and acanthosis nigricans (type C insulin resistance)H Globerman, E Karnieli
Scandinavian Journal of Haematology|October 1, 1984
Haemolysis in a G6PD-deficient child induced by eating unripe peachesH Globerman, T Navok, M Chevion
The American Journal of Pediatric Hematology/Oncology|January 1, 1991
A xanthogranulomatous histiocytosis in a child presenting with short statureH Globerman, S Burstein, P J Girardina, et al.
The Journal of Biological Chemistry|September 15, 1993
Expression and purification of functional human 17 alpha-hydroxylase/17,20-lyase (P450c17) in Escherichia coli. Use of this system for study of a novel form of combined 17 alpha-hydroxylase/17,20-lyase deficiencyT Imai, H Globerman, J M Gertner, et al.
The New England Journal of Medicine|November 3, 1988
An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylaseH Globerman, A Rösler, R Theodor, et al.
The Journal of Clinical Investigation|July 1, 1988
Nonsense mutation causing steroid 21-hydroxylase deficiencyH Globerman, M Amor, K L Parker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiencyM Amor, K L Parker, H Globerman, et al.
Clinical Endocrinology|April 13, 2000
Analysis of the peroxisome proliferator activated receptor gamma (PPARgamma) gene in HAIRAN syndrome with obesityH Globerman, Y Zauberman, T Makarov, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 13, 1998
Analysis of the insulin receptor gene tyrosine kinase domain in obese patients with hyperandrogenism, insulin resistance and acanthosis nigricans (type C insulin resistance)H Globerman, E Karnieli
Scandinavian Journal of Haematology|October 1, 1984
Haemolysis in a G6PD-deficient child induced by eating unripe peachesH Globerman, T Navok, M Chevion
The American Journal of Pediatric Hematology/Oncology|January 1, 1991
A xanthogranulomatous histiocytosis in a child presenting with short statureH Globerman, S Burstein, P J Girardina, et al.
The Journal of Biological Chemistry|September 15, 1993
Expression and purification of functional human 17 alpha-hydroxylase/17,20-lyase (P450c17) in Escherichia coli. Use of this system for study of a novel form of combined 17 alpha-hydroxylase/17,20-lyase deficiencyT Imai, H Globerman, J M Gertner, et al.
The New England Journal of Medicine|November 3, 1988
An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylaseH Globerman, A Rösler, R Theodor, et al.
The Journal of Clinical Investigation|July 1, 1988
Nonsense mutation causing steroid 21-hydroxylase deficiencyH Globerman, M Amor, K L Parker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiencyM Amor, K L Parker, H Globerman, et al.
Clinical Endocrinology|April 13, 2000
Analysis of the peroxisome proliferator activated receptor gamma (PPARgamma) gene in HAIRAN syndrome with obesityH Globerman, Y Zauberman, T Makarov, et al.
Pageof 1