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L Beaudet

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Biochemistry|May 12, 1981
Increased translatable messenger ribonucleic acid for argininosuccinate synthetase in canavanine-resistant human cellsT S Su, A L Beaudet, W E O'Brien
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1983
Stable low molecular weight DNA in xeroderma pigmentosum cellsM M Hurt, A L Beaudet, R E Moses
The Journal of Biological Chemistry|September 25, 1980
Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase systemA J Lange, W J Arion, A L Beaudet
Genes & Development|October 18, 2006
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domainMei-Yi Wu, Ting-Fen Tsai, Arthur L Beaudet
Methods in Enzymology|January 1, 1974
Mammalian release factor; in vitro assay and purificationC T Caskey, A L Beaudet, W P Tate
Nucleic Acids Research|July 11, 1989
Nucleotide sequence of the cDNA from the mouse leukocyte adhesion protein CD18R W Wilson, W E O'Brien, A L Beaudet
Human Molecular Genetics|December 10, 2002
A gene fusion method to screen for regulatory effects on gene expression: application to the LDL receptorKaiyi Li, Maricela A Ramirez, Esmie Rose, et al.
Somatic Cell and Molecular Genetics|January 1, 1994
Generation of a mouse model for citrullinemia by targeted disruption of the argininosuccinate synthetase geneG Patejunas, A Bradley, A L Beaudet, et al.
The Journal of Pediatrics|February 1, 1986
Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiencyM L Batshaw, M Msall, A L Beaudet, et al.
Molecular Biology & Medicine|February 1, 1991
Additional mutations in argininosuccinate synthetase causing citrullinemiaK Kobayashi, C Rosenbloom, A L Beaudet, et al.
Pageof 46

Showing results (111-120 of 456) with videos related to

Sort By:
Pageof 46
Biochemistry|May 12, 1981
Increased translatable messenger ribonucleic acid for argininosuccinate synthetase in canavanine-resistant human cellsT S Su, A L Beaudet, W E O'Brien
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1983
Stable low molecular weight DNA in xeroderma pigmentosum cellsM M Hurt, A L Beaudet, R E Moses
The Journal of Biological Chemistry|September 25, 1980
Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase systemA J Lange, W J Arion, A L Beaudet
Genes & Development|October 18, 2006
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domainMei-Yi Wu, Ting-Fen Tsai, Arthur L Beaudet
Methods in Enzymology|January 1, 1974
Mammalian release factor; in vitro assay and purificationC T Caskey, A L Beaudet, W P Tate
Nucleic Acids Research|July 11, 1989
Nucleotide sequence of the cDNA from the mouse leukocyte adhesion protein CD18R W Wilson, W E O'Brien, A L Beaudet
Human Molecular Genetics|December 10, 2002
A gene fusion method to screen for regulatory effects on gene expression: application to the LDL receptorKaiyi Li, Maricela A Ramirez, Esmie Rose, et al.
Somatic Cell and Molecular Genetics|January 1, 1994
Generation of a mouse model for citrullinemia by targeted disruption of the argininosuccinate synthetase geneG Patejunas, A Bradley, A L Beaudet, et al.
The Journal of Pediatrics|February 1, 1986
Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiencyM L Batshaw, M Msall, A L Beaudet, et al.
Molecular Biology & Medicine|February 1, 1991
Additional mutations in argininosuccinate synthetase causing citrullinemiaK Kobayashi, C Rosenbloom, A L Beaudet, et al.
Pageof 46