Zobrazeno 1 - 10
of 19
pro vyhledávání: '"S C, Chandrasekharappa"'
Autor:
Bin Tean Teh, S. C Chandrasekharappa
Publikováno v:
Journal of Internal Medicine. 253:606-615
Multiple endocrine neoplasia type 1 is an autosomal dominant cancer syndrome affecting primarily parathyroid, enteropancreatic endocrine and pituitary tissues. The inactivating germline and somatic mutations spread throughout the gene and the accompa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef948df71d01256a2138c5d2daa3783
https://doi.org/10.1046/j.1365-2796.2003.01165.x
https://doi.org/10.1046/j.1365-2796.2003.01165.x
Publikováno v:
The Journal of Immunology. 157:5461-5466
Fas-associated death domain protein (FADD)/MORT1 is a 23-kDa cytoplasmic protein containing a C-terminal death domain that interacts with the intracellular death domain of the Fas transmembrane receptor. Cross-linking of Fas mediates apoptosis in a v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::697a1bae0843242178f3bc351f0b21fe
https://doi.org/10.4049/jimmunol.157.12.5461
https://doi.org/10.4049/jimmunol.157.12.5461
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 12
The technology of cloning large fragments of DNA in yeast as yeast artificial chromosomes (YACs) (1), combined with that of electro-phoretic separation of large fragments by pulsed-field gel electrophoresis (PFGE), has revolutionized research in mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89058b6930ecea861137febccd55ddb1
https://pubmed.ncbi.nlm.nih.gov/21409638
https://pubmed.ncbi.nlm.nih.gov/21409638
Autor:
S C, Chandrasekharappa, B T, Teh
Publikováno v:
Frontiers of hormone research. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::681ee216651e1c3187d0198a47d4ae73
https://pubmed.ncbi.nlm.nih.gov/11443853
https://pubmed.ncbi.nlm.nih.gov/11443853
Autor:
E S, Srivatsan, U, Bengtsson, P, Manickam, P, Benyamini, S C, Chandrasekharappa, C, Sun, E J, Stanbridge, J L, Redpath
Publikováno v:
Genes, chromosomescancer. 29(2)
Previous cytogenetic and molecular genetic studies have shown that the HeLa (cervical carcinoma) cell line D98/AH-2 contains two apparently normal copies of chromosome 11 and additional 11q13-25 material translocated onto a chromosome 3 marker. To de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58e7adffd5b912e1e214cd322fb32309
https://pubmed.ncbi.nlm.nih.gov/10959095
https://pubmed.ncbi.nlm.nih.gov/10959095
Autor:
T, Oda, A G, Elkahloun, P S, Meltzer, K, Okajima, K, Sugiyama, Y, Wada, S C, Chandrasekharappa
Publikováno v:
Human mutation. 16(1)
Alagille syndrome (AGS) is an autosomal dominant, developmental disorder affecting multiple organ systems including liver, heart, vertebrae, eye and face. Recurrent deletions of the 20p12 region led to the localization, and ultimately to the identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d60828387d5a6986f41695a335ba80d0
https://pubmed.ncbi.nlm.nih.gov/10874319
https://pubmed.ncbi.nlm.nih.gov/10874319
Autor:
L V, Debelenko, J I, Swalwell, M J, Kelley, E, Brambilla, P, Manickam, G, Baibakov, S K, Agarwal, A M, Spiegel, S J, Marx, S C, Chandrasekharappa, F S, Collins, W D, Travis, M R, Emmert-Buck
Publikováno v:
Genes, chromosomescancer. 28(1)
Neuroendocrine tumors of the lung consist of a spectrum of neoplasms, including typical carcinoids, atypical carcinoids, large-cell neuroendocrine carcinomas (LCNEC), and small-cell lung carcinomas (SCLC). We previously reported frequent inactivation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e51b08061743f970f93f0f992661a73e
https://pubmed.ncbi.nlm.nih.gov/10738303
https://pubmed.ncbi.nlm.nih.gov/10738303
Autor:
S J, Marx, S K, Agarwal, M B, Kester, C, Heppner, Y S, Kim, M C, Skarulis, L A, James, P K, Goldsmith, S K, Saggar, S Y, Park, A M, Spiegel, A L, Burns, L V, Debelenko, Z, Zhuang, I A, Lubensky, L A, Liotta, M R, Emmert-Buck, S C, Guru, P, Manickam, J, Crabtree, M R, Erdos, F S, Collins, S C, Chandrasekharappa
Publikováno v:
Recent progress in hormone research. 54
MEN1 is a syndrome of parathyroid adenomas, gastrinomas, prolactinomas, and other endocrine tumors. Collagenomas and facial angiofibromas are newly recognized but common skin expressions. Many tumors in MEN1 are benign; however, many entero-pancreati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::80b79b978e3f3c52e760c0e6180d890b
https://pubmed.ncbi.nlm.nih.gov/10548885
https://pubmed.ncbi.nlm.nih.gov/10548885
Autor:
V, Srikantan, I A, Sesterhenn, L, Davis, G R, Hankins, F A, Avallone, J R, Livezey, R, Connelly, F K, Mostofi, D G, McLeod, J W, Moul, S C, Chandrasekharappa, S, Srivastava
Publikováno v:
International journal of cancer. 84(3)
Molecular genetic analyses of human prostate cancer (CaP) has revealed frequent loss of specific chromosome regions suggesting the presence of putative tumor suppressor gene(s) (TSG) on these chromosome loci whose inactivation may play a role in pros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df589a972c0633654c82cdbda2aa60e9
https://pubmed.ncbi.nlm.nih.gov/10371356
https://pubmed.ncbi.nlm.nih.gov/10371356
Autor:
S K, Agarwal, L V, Debelenko, M B, Kester, S C, Guru, P, Manickam, S E, Olufemi, M C, Skarulis, C, Heppner, J S, Crabtree, I A, Lubensky, Z, Zhuang, Y S, Kim, S C, Chandrasekharappa, F S, Collins, L A, Liotta, A M, Spiegel, A L, Burns, M R, Emmert-Buck, S J, Marx
Publikováno v:
Human mutation. 12(2)
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder that manifests as varying combinations of tumors of endocrine and other tissues (parathyroids, pancreatic islets, duodenal endocrine cells, the anterior pituitary and others
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::367ee1d8acb7661bf69ad39c2f8b6683
https://pubmed.ncbi.nlm.nih.gov/9671267
https://pubmed.ncbi.nlm.nih.gov/9671267