Zobrazeno 1 - 10
of 376
pro vyhledávání: '"Sj Meltzer"'
Publikováno v:
BJOG: An International Journal of Obstetrics & Gynaecology. 117:407-415
Please cite this paper as: Meltzer S, Snyder J, Penrod J, Nudi M, Morin L. Gestational diabetes mellitus screening and diagnosis: a prospective randomised controlled trial comparing costs of one-step and two-step methods. BJOG 2010;117:407–415. Obj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa01338f4b69748da88a9d9824555538
https://doi.org/10.1111/j.1471-0528.2009.02475.x
https://doi.org/10.1111/j.1471-0528.2009.02475.x
Autor:
Garrett M. Brodeur, Patricia E. Berg, C. N. Frantz, K Smolinski, J Liu, Alan B. Cantor, Marcus B. Valentine, Jing Yin, SJ Meltzer, SP O'Doherty
Publikováno v:
British Journal of Cancer
Neuroblastoma is the most common extracranial solid tumour of childhood. Amplification of the proto-oncogene, N-myc, confers a poor prognosis in neuroblastoma, while hyperdiploidy is associated with a favourable outcome. Little is known about the con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d700319cc3710304644047a187d8990
https://doi.org/10.1038/bjc.1996.645
https://doi.org/10.1038/bjc.1996.645
Autor:
Esteller M, Cordon-Cardo C, Pg, Corn, Sj, Meltzer, Ks, Pohar, Dn, Watkins, Capella G, Miguel A. Peinado, Matias-Guiu X, Prat J, Sb, Baylin, Jg, Herman
Publikováno v:
Europe PubMed Central
The INK4a/ARF locus encodes two distinct tumor suppressors, p16INK4a and p14ARF. Although the contribution of p16INK4a to human tumorigenesis through point mutation, deletion, and hypermethylation has been widely documented, little is known about spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::de2a554afa4eb754e8d5cd0572c48cee
https://pubmed.ncbi.nlm.nih.gov/11306450
https://pubmed.ncbi.nlm.nih.gov/11306450
Autor:
Esteller M, Sparks A, Toyota M, Sanchez-Cespedes M, Capella G, Miguel A. Peinado, Gonzalez S, Tarafa G, Sidransky D, Sj, Meltzer, Sb, Baylin, Jg, Herman
Publikováno v:
ResearcherID
Scopus-Elsevier
Europe PubMed Central
Scopus-Elsevier
Europe PubMed Central
Germ-line mutations in the tumor suppressor gene APC are associated with hereditary familial adenomatous polyposis (FAP), and somatic mutations are common in sporadic colorectal tumors. We now report that methylation in the promoter region of this ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::bab028cfa7c2f29fc6f81999b51d3870
https://pubmed.ncbi.nlm.nih.gov/10969779
https://pubmed.ncbi.nlm.nih.gov/10969779
Hypermethylation of the hMLH1 gene promoter in human gastric cancers with microsatellite instability
Autor:
As, Fleisher, Manel Esteller, Wang S, Tamura G, Suzuki H, Yin J, Tt, Zou, Jm, Abraham, Kong D, Kn, Smolinski, Yq, Shi, Mg, Rhyu, Sm, Powell, Sp, James, Kt, Wilson, Jg, Herman, Sj, Meltzer
Publikováno v:
Europe PubMed Central
Human gastric carcinoma shows a higher prevalence of microsatellite instability (MSI) than does any other type of sporadic human cancer. The reasons for this high frequency of MSI are not yet known. In contrast to endometrial and colorectal carcinoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c4fd30a2748cf8c594078b0d5375ab91
https://pubmed.ncbi.nlm.nih.gov/10070967
https://pubmed.ncbi.nlm.nih.gov/10070967
Publikováno v:
International Journal of Oncology.
Barrett's esophagus is a recognized risk factor for adenocarcinoma of the esophagus. Dysplasia in Barrett's epithelium is considered a precursor to malignancy. Several tumor suppressor genes, including p53, have recently been implicated in the pathog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::229dea60d51987c1e11b04c5a523c151
https://doi.org/10.3892/ijo.1.3.271
https://doi.org/10.3892/ijo.1.3.271
Autor:
Mori Y, Yin J, Rashid A, Ba, Leggett, Young J, Lisa Simms, Pm, Kuehl, Langenberg P, Sj, Meltzer, Oc, Stine
Publikováno v:
Europe PubMed Central
Coding region frameshift mutation caused by microsatellite instability (MSI) is one mechanism contributing to tumorigenesis in cancers with MSI in high frequency. Mutation of TGFBR2 is one example of this process. To identify additional examples, a l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b9a3737e8954838a953b671eaa7e915e
http://europepmc.org/abstract/med/11507051
http://europepmc.org/abstract/med/11507051
Autor:
Rf, Souza, Laure Garrigue-Antar, Lei J, Yin J, Appel R, Vf, Vellucci, Tt, Zou, Zhou X, Wang S, Mg, Rhyu, Cymes K, Chan O, Ws, Park, Mj, Krasna, Bd, Greenwald, Cottrell J, Jm, Abraham, Simms L, Leggett B, Sj, Meltzer
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c578bd69d9a8553bec98c5542b21ce5d
http://europepmc.org/abstract/med/9183654
http://europepmc.org/abstract/med/9183654
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::000b841e2dc1f6354c9c22f3e3191ec3
http://europepmc.org/abstract/med/12384567
http://europepmc.org/abstract/med/12384567
Autor:
Dm, Shibata, Sato F, Mori Y, Perry K, Yin J, Wang S, Xu Y, Olaru A, Selaru F, Kevin Spring, Young J, Jm, Abraham, Sj, Meltzer
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6e2f94f2fd95a5353664609b66cb1480
http://www.scopus.com/inward/record.url?eid=2-s2.0-0037108915&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0037108915&partnerID=MN8TOARS