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

R L Nussbaum

Showing results (51-60 of 115) with videos related to

Pageof 12
Sort By:
The Journal of Biological Chemistry|April 10, 1999
Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110alpha subunit of phosphoinositide 3-kinaseL Bi, I Okabe, D J Bernard, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|January 20, 2000
Ocrl1, a PtdIns(4,5)P(2) 5-phosphatase, is localized to the trans-Golgi network of fibroblasts and epithelial cellsM A Dressman, I M Olivos-Glander, R L Nussbaum, et al.
Genomics|March 1, 1992
Construction and characterization of a yeast artificial chromosome library for Xpter-Xq27.3: a systematic determination of cocloning rate and X-chromosome representationJ T Lee, A Murgia, D M Sosnoski, et al.
Genomics|March 1, 1993
Deletion mapping and a highly reduced radiation hybrid in the Xp22.3-p22.2 regionR E Schnur, P A Wick, D N Sosnoski, et al.
Genetics|October 1, 1995
Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosomeR J Oakey, P G Matteson, S Litwin, et al.
The Journal of Clinical Investigation|September 1, 1983
Human hypoxanthine-guanine phosphoribosyltransferase. Detection of a mutant allele by restriction endonuclease analysisJ M Wilson, P Frossard, R L Nussbaum, et al.
Prenatal Diagnosis|December 17, 1998
First report of prenatal biochemical diagnosis of Lowe syndromeS F Suchy, T Lin, J A Horwitz, et al.
Human Genetics|February 1, 1997
Physical mapping and genomic structure of the Lowe syndrome gene OCRL1R L Nussbaum, B M Orrison, P A Jänne, et al.
American Journal of Diseases of Children (1960)|January 1, 1984
Newborn screening for sickling hemoglobinopathies. Houston, 1976 to 1980R L Nussbaum, C Powell, H L Graham, et al.
Molecular Genetics and Metabolism|July 31, 1998
Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patientsT Lin, B M Orrison, S F Suchy, et al.
Pageof 12

Showing results (51-60 of 115) with videos related to

Sort By:
Pageof 12
The Journal of Biological Chemistry|April 10, 1999
Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110alpha subunit of phosphoinositide 3-kinaseL Bi, I Okabe, D J Bernard, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|January 20, 2000
Ocrl1, a PtdIns(4,5)P(2) 5-phosphatase, is localized to the trans-Golgi network of fibroblasts and epithelial cellsM A Dressman, I M Olivos-Glander, R L Nussbaum, et al.
Genomics|March 1, 1992
Construction and characterization of a yeast artificial chromosome library for Xpter-Xq27.3: a systematic determination of cocloning rate and X-chromosome representationJ T Lee, A Murgia, D M Sosnoski, et al.
Genomics|March 1, 1993
Deletion mapping and a highly reduced radiation hybrid in the Xp22.3-p22.2 regionR E Schnur, P A Wick, D N Sosnoski, et al.
Genetics|October 1, 1995
Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosomeR J Oakey, P G Matteson, S Litwin, et al.
The Journal of Clinical Investigation|September 1, 1983
Human hypoxanthine-guanine phosphoribosyltransferase. Detection of a mutant allele by restriction endonuclease analysisJ M Wilson, P Frossard, R L Nussbaum, et al.
Prenatal Diagnosis|December 17, 1998
First report of prenatal biochemical diagnosis of Lowe syndromeS F Suchy, T Lin, J A Horwitz, et al.
Human Genetics|February 1, 1997
Physical mapping and genomic structure of the Lowe syndrome gene OCRL1R L Nussbaum, B M Orrison, P A Jänne, et al.
American Journal of Diseases of Children (1960)|January 1, 1984
Newborn screening for sickling hemoglobinopathies. Houston, 1976 to 1980R L Nussbaum, C Powell, H L Graham, et al.
Molecular Genetics and Metabolism|July 31, 1998
Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patientsT Lin, B M Orrison, S F Suchy, et al.
Pageof 12