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R L Nussbaum

Showing results (31-40 of 115) with videos related to

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Journal of Inherited Metabolic Disease|January 28, 2009
Abnormal bradykinin signalling in fibroblasts deficient in the PIP(2) 5-phosphatase, ocrl1S F Suchy, J C Cronin, R L Nussbaum
American Journal of Human Genetics|April 1, 1992
Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: normal women versus carriers of X-linked severe combined immunodeficiencyJ M Puck, C C Stewart, R L Nussbaum
Texas Heart Institute Journal|March 1, 1984
A case of myocardial infarction in a patient with Werner's syndromeS F Soto-Figueroa, R L Nussbaum, E Garcia
Human Molecular Genetics|April 1, 1993
Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of LoweA M Leahey, L R Charnas, R L Nussbaum
Human Genetics|January 1, 1983
Expression of the fragile (X) chromosome in an interspecific somatic cell hybridR L Nussbaum, S D Airhart, D H Ledbetter
American Journal of Human Genetics|October 1, 1995
The oculocerebrorenal syndrome gene product is a 105-kD protein localized to the Golgi complexI M Olivos-Glander, P A Jänne, R L Nussbaum
Cell|July 30, 1993
The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding proteinH Siomi, M C Siomi, R L Nussbaum, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
Southern analysis of the Lesch-Nyhan locus in manR L Nussbaum, C T Caskey, F Gilbert, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|February 24, 2001
Cloning and genomic organization of the mouse gene slc23a1 encoding a vitamin C transporterS Gispert, A Dutra, A Lieberman, et al.
Clinical Genetics|November 1, 1980
Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutationC T Caskey, R L Nussbaum, L C Cohan, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|January 28, 2009
Abnormal bradykinin signalling in fibroblasts deficient in the PIP(2) 5-phosphatase, ocrl1S F Suchy, J C Cronin, R L Nussbaum
American Journal of Human Genetics|April 1, 1992
Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: normal women versus carriers of X-linked severe combined immunodeficiencyJ M Puck, C C Stewart, R L Nussbaum
Texas Heart Institute Journal|March 1, 1984
A case of myocardial infarction in a patient with Werner's syndromeS F Soto-Figueroa, R L Nussbaum, E Garcia
Human Molecular Genetics|April 1, 1993
Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of LoweA M Leahey, L R Charnas, R L Nussbaum
Human Genetics|January 1, 1983
Expression of the fragile (X) chromosome in an interspecific somatic cell hybridR L Nussbaum, S D Airhart, D H Ledbetter
American Journal of Human Genetics|October 1, 1995
The oculocerebrorenal syndrome gene product is a 105-kD protein localized to the Golgi complexI M Olivos-Glander, P A Jänne, R L Nussbaum
Cell|July 30, 1993
The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding proteinH Siomi, M C Siomi, R L Nussbaum, et al.
Advances in Experimental Medicine and Biology|January 1, 1984
Southern analysis of the Lesch-Nyhan locus in manR L Nussbaum, C T Caskey, F Gilbert, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|February 24, 2001
Cloning and genomic organization of the mouse gene slc23a1 encoding a vitamin C transporterS Gispert, A Dutra, A Lieberman, et al.
Clinical Genetics|November 1, 1980
Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutationC T Caskey, R L Nussbaum, L C Cohan, et al.
Pageof 12