Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Elizabeth A. Novotny"'
Autor:
Settara C. Chandrasekharappa, Francis S. Collins, Stephen J. Marx, Sunita K. Agarwal, Mon-Li Chu, Rui-Zhu Zhang, Yidong Chen, Abdel Elkahloun, Sukhbir Kaur, Elizabeth A. Novotny, Nijaguna B. Prasad, Youngmi Ji
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome characterized primarily by endocrine tumors of the parathyroids, anterior pituitary, and enteropancreatic endocrine tissues. Affected individuals carry a ger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bbf5494644389dc043ae8356909a3da
https://doi.org/10.1158/1541-7786.c.6542847
https://doi.org/10.1158/1541-7786.c.6542847
Autor:
Settara C. Chandrasekharappa, Francis S. Collins, Stephen J. Marx, Sunita K. Agarwal, Mon-Li Chu, Rui-Zhu Zhang, Yidong Chen, Abdel Elkahloun, Sukhbir Kaur, Elizabeth A. Novotny, Nijaguna B. Prasad, Youngmi Ji
Supplementary Table S1 from Mouse Embryo Fibroblasts Lacking the Tumor Suppressor Menin Show Altered Expression of Extracellular Matrix Protein Genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::855c6f2c9076956b52ded86c9185007f
https://doi.org/10.1158/1541-7786.22520946.v1
https://doi.org/10.1158/1541-7786.22520946.v1
Autor:
Pengfei Liu, Francis S. Collins, Settara C. Chandrasekharappa, Elizabeth A. Novotny, Sheila T. Compton
Publikováno v:
Mechanisms of Development. 126(7):517-522
Inactivating mutations in the tumor suppressor gene MEN1 cause the inherited cancer syndrome multiple endocrine neoplasia type 1 (MEN1). The ubiquitously expressed MEN1 encoded protein, menin, interacts with MLL (mixed-lineage leukemia protein), and
Autor:
Nijaguna B. Prasad, Abdel G. Elkahloun, Rui Zhu Zhang, Francis S. Collins, Settara C. Chandrasekharappa, Sukhbir Kaur, Elizabeth A. Novotny, Youngmi Ji, Yi Chen, Sunita K. Agarwal, Stephen J. Marx, Mon-Li Chu
Publikováno v:
Molecular Cancer Research. 5:1041-1051
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome characterized primarily by endocrine tumors of the parathyroids, anterior pituitary, and enteropancreatic endocrine tissues. Affected individuals carry a ger
Autor:
Frank H. Collins, Youngmi Ji, Peter C. Scacheri, Carmen M. Mateo, Allen M. Spiegel, Steven K. Libutti, Settara C. Chandrasekharappa, S. Rao, Brian Oliver, Alison B. Hickman, A L Burns, Aniello Cerrato, Elizabeth A. Novotny, Patricia A. Kennedy, Terri S. Rice, Sunita K. Agarwal, J.B. Moore, Stephen J. Marx
Publikováno v:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 37(6)
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disease predisposed by heterozygous germline mutations in the MEN1 tumor suppressor gene. Biallelic loss of MEN1 resulting from small mutation and/or loss of heterozygosity occurs in
Autor:
Michael E. Mullendore, Alison B. Hickman, Judy S. Crabtree, Youngmi Ji, Aniello Cerrato, Jerrold M. Ward, H. Richard Alexander, William F. Simonds, Brian Oliver, Sonia Santa Anna-A, Carmen M. Mateo, A. Lee Burns, Peter C. Scacheri, Victor H. Obungu, Ira Whitten, Karen E. Sukhodolets, Sunita K. Agarwal, Michael Parisi, Stephen J. Marx, Allen M. Spiegel, Francis S. Collins, Elizabeth A. Novotny, Patricia A. Kennedy, Settara C. Chandrasekharappa, Monica C. Skarulis, Lisa Garrett-Beal, Steven K. Libutti
Publikováno v:
Annals of the New York Academy of Sciences. 1014
Multiple endocrine neoplasia type 1 (MEN1), among all syndromes, causes tumors in the highest number of tissue types. Most of the tumors are hormone producing (e.g., parathyroid, enteropancreatic endocrine, anterior pituitary) but some are not (e.g.,
Autor:
Maxim V. Sukhodolets, Settara C. Chandrasekharappa, Francis S. Collins, Alison B. Hickman, Elizabeth A. Novotny, Sunita K. Agarwal, Stephen J. Marx, Allen M. Spiegel, Victor H. Obungu, A. Lee Burns, Judy S. Crabtree, Karen E. Sukhodolets
Publikováno v:
Molecular and cellular biology. 23(2)
Menin is a 70-kDa protein encoded by MEN1, the tumor suppressor gene disrupted in multiple endocrine neoplasia type 1. In a yeast two-hybrid system based on reconstitution of Ras signaling, menin was found to interact with the 32-kDa subunit (RPA2) o
Autor:
Joseph G. Hacia, Stephen A. Woski, Melissa A. Ashlock, Francis S. Collins, Elizabeth A. Novotny, R. Aeryn Mayer
Publikováno v:
Nucleic acids research. 27(20)
A series of dye-labeled oligonucleotide probes containing base and sugar modifications were tested for the ability to detect telomeric repeat sequences in FISH assays. These modified oligonucleotides, all 18 nt in length, were complementary to either
Autor:
Xin Yuan Guan, Pengfei Liu, Melissa A. Ashlock, Elizabeth A. Novotny, Sheila T. Compton, Karla A. Henning
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 96(2)
A human artificial chromosome (HAC) vector was constructed from a 1-Mb yeast artificial chromosome (YAC) that was selected based on its size from among several YACs identified by screening a randomly chosen subset of the Centre d’Étude du Polymorp
Autor:
William B. Guggino, Yuan Jiang, Michael L. Bittner, Karla A. Henning, Elizabeth A. Novotny, Melissa A. Rosenfeld, Peter J. Mogayzel, Erik M. Schwiebert
Publikováno v:
Human molecular genetics. 6(1)
The cystic fibrosis transmembrane conductance regulator gene (CFTR) encodes a transmembrane protein (CFTR) which functions in part as a cyclic adenosine monophosphate (cAMP)-regulated chloride channel. CFTR expression is controlled temporally and cel