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Diabetologia|March 4, 1999

The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sampleS Ghosh, C D Langefeld, D Ally, et al.

Human Mutation|April 29, 1998

Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from NewfoundlandS E Olufemi, J S Green, P Manickam, et al.

Cell|February 16, 1999

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcriptionS K Agarwal, S C Guru, C Heppner, et al.

Genomics|April 15, 1996

A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23K Savitsky, Y Ziv, A Bar-Shira, et al.

The Journal of Clinical Endocrinology and Metabolism|May 1, 1997

Loss of heterozygosity at 11q13: analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1Q Dong, L V Debelenko, S C Chandrasekharappa, et al.

Cancer Research|November 15, 1996

Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN1 patientsI A Lubensky, L V Debelenko, Z Zhuang, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001

A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumorsJ S Crabtree, P C Scacheri, J M Ward, et al.

Genes, Chromosomes & Cancer|March 30, 2000

MEN1 gene mutation analysis of high-grade neuroendocrine lung carcinomaL V Debelenko, J I Swalwell, M J Kelley, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 26, 1999

Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 geneS C Guru, J S Crabtree, K D Brown, et al.

Diabetes|April 6, 2001

The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differencesJ A Douglas, M R Erdos, R M Watanabe, et al.

Pageof 24

Showing results (191-200 of 234) with videos related to

Sort By:

Pageof 24

Diabetologia|March 4, 1999

The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sampleS Ghosh, C D Langefeld, D Ally, et al.

Human Mutation|April 29, 1998

Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from NewfoundlandS E Olufemi, J S Green, P Manickam, et al.

Cell|February 16, 1999

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcriptionS K Agarwal, S C Guru, C Heppner, et al.

Genomics|April 15, 1996

A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23K Savitsky, Y Ziv, A Bar-Shira, et al.

The Journal of Clinical Endocrinology and Metabolism|May 1, 1997

Loss of heterozygosity at 11q13: analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1Q Dong, L V Debelenko, S C Chandrasekharappa, et al.

Cancer Research|November 15, 1996

Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN1 patientsI A Lubensky, L V Debelenko, Z Zhuang, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001

A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumorsJ S Crabtree, P C Scacheri, J M Ward, et al.

Genes, Chromosomes & Cancer|March 30, 2000

MEN1 gene mutation analysis of high-grade neuroendocrine lung carcinomaL V Debelenko, J I Swalwell, M J Kelley, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 26, 1999

Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 geneS C Guru, J S Crabtree, K D Brown, et al.

Diabetes|April 6, 2001

The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differencesJ A Douglas, M R Erdos, R M Watanabe, et al.

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