Zobrazeno 1 - 10
of 12
pro vyhledávání: '"S D, Pack"'
Autor:
S. D. Pack
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 85:3860-3865
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3bdef7f014677404fbaff1b78ecc273
https://doi.org/10.1210/jc.85.10.3860
https://doi.org/10.1210/jc.85.10.3860
Publikováno v:
Methods in molecular medicine. 50
An opportunity to look inside of the individual cell for the direct visualization in situ of "what happened?" is the most wonderful feature offered by fluorescence in situ hybridization (FISH). DNA in situ hybridization is a technique that allows the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f76e370e9309a888d33a5c2bfbd311c7
https://pubmed.ncbi.nlm.nih.gov/21318814
https://pubmed.ncbi.nlm.nih.gov/21318814
Autor:
C A, Stratakis, D H, Schussheim, S M, Freedman, M F, Keil, S D, Pack, S K, Agarwal, M C, Skarulis, R J, Weil, I A, Lubensky, Z, Zhuang, E H, Oldfield, S J, Marx
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(12)
Multiple endocrine neoplasia type 1 (MEN 1) is associated with parathyroid, enteropancreatic, pituitary, and other tumors. The MEN1 gene, a tumor suppressor, is located on chromosome 11. Affected individuals inherit a mutated MEN1 allele, and tumorig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e5caefac14081e1371bf58a46622c04
https://pubmed.ncbi.nlm.nih.gov/11134142
https://pubmed.ncbi.nlm.nih.gov/11134142
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(10)
Carney complex (CNC) is a familial multiple neoplasia and lentiginosis syndrome with features overlapping those of McCune-Albright syndrome (MAS) and other multiple endocrine neoplasia (MEN) syndromes, MEN type 1 (MEN 1), in particular. GH-producing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::557e8102c87d1cf22c6ccc36fe1efca5
https://pubmed.ncbi.nlm.nih.gov/11061550
https://pubmed.ncbi.nlm.nih.gov/11061550
Autor:
S D, Pack, B, Zbar, E, Pak, D O, Ault, J S, Humphrey, T, Pham, K, Hurley, R J, Weil, W S, Park, I, Kuzmin, C, Stolle, G, Glenn, L A, Liotta, M I, Lerman, R D, Klausner, W M, Linehan, Z, Zhuang
Publikováno v:
Cancer research. 59(21)
von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited cancer syndrome predisposing to a variety of tumor types that include retinal hemangioblastomas, hemangioblastomas of the central nervous system, renal cell carcinomas, pancreatic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d1d89282b08ec6895d5e104202114d8
https://pubmed.ncbi.nlm.nih.gov/10554035
https://pubmed.ncbi.nlm.nih.gov/10554035
Autor:
S D, Pack, J D, Karkera, Z, Zhuang, E D, Pak, K V, Balan, P, Hwu, W S, Park, T, Pham, D O, Ault, M, Glaser, L, Liotta, S D, Detera-Wadleigh, R G, Wadleigh
Publikováno v:
Genes, chromosomescancer. 25(2)
Esophageal cancer is the third most prevalent gastrointestinal malignancy in the world. The tumor responds poorly to various therapeutic regimens and the genetic events underlying esophageal carcinogenesis are not well understood. To identify overall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8e9bae237f99dc5633741a58df5a8486
https://pubmed.ncbi.nlm.nih.gov/10338000
https://pubmed.ncbi.nlm.nih.gov/10338000
Publikováno v:
Cytogenetics and cell genetics. 83(1-2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dec497049b5f2f342b9448402a093558
https://pubmed.ncbi.nlm.nih.gov/9925933
https://pubmed.ncbi.nlm.nih.gov/9925933
Publikováno v:
Cancer research. 59(2)
Although neoplasia is caused by clonal proliferation of cells, the resulting tumors are frequently heterogeneous, being composed of both neoplastic and reactive cells. Therefore, identification of tumors as neoplastic processes is frequently obscured
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d4f9b99e2b174f066d59bfccb80e72b
https://pubmed.ncbi.nlm.nih.gov/9927030
https://pubmed.ncbi.nlm.nih.gov/9927030
Autor:
L D, Matyakhina, I V, Koroleva, S N, Malchenko, C, Bendixen, O V, Cheryaukene, S D, Pack, P M, Borodin, O L, Serov, J B, Searle
Publikováno v:
Cytogenetics and cell genetics. 77(3-4)
This report extends the genetic map of the common shrew (Sorex araneus) by use of a clone panel of shrew-Chinese hamster and shrew-mouse hybrid cells (Pack et al., 1995; Matyakhina et al., 1996). This set of hybrid clones made it possible to assign t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::02a05308ba161177bcf6db7c62227788
https://pubmed.ncbi.nlm.nih.gov/9284916
https://pubmed.ncbi.nlm.nih.gov/9284916
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 7(4)
This report extends the genetic map of the common shrew (Sorex araneus) by adding chromosome assignments for ten genes to the seven already mapped (Pack et al. 1995). A somatic cell hybrid panel was used for the mapping. The genes for peptidase A (PE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8228e21703ca40cc84c6861337477ac
https://pubmed.ncbi.nlm.nih.gov/8661695
https://pubmed.ncbi.nlm.nih.gov/8661695