Zobrazeno 1 - 10
of 30
pro vyhledávání: '"J E, Garber"'
Autor:
John R. Walker, Matthew T Bernstein, Harminder Singh, J E Garber, P Faucher, Kristin Reynolds
BACKGROUND: Preferences for receipt of information vary among individuals, with many patients showing an interest in receiving via video content. Although several educational videos on colonoscopy are available, most of them have not been evaluated s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e982e40b4c38b2ec6691c9eed4a4add9
https://europepmc.org/articles/PMC6512665/
https://europepmc.org/articles/PMC6512665/
Autor:
S B, Lee, S H, Kim, D W, Bell, D C, Wahrer, T A, Schiripo, M M, Jorczak, D C, Sgroi, J E, Garber, F P, Li, K E, Nichols, J M, Varley, A K, Godwin, K M, Shannon, E, Harlow, D A, Haber
Publikováno v:
Cancer research. 61(22)
Li Fraumeni Syndrome (LFS) is a multicancer phenotype, most commonly associated with germ-line mutations in TP53. In a kindred with LFS without an inherited TP53 mutation, we have previously reported a truncating mutation (1100delC) in CHK2, encoding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ceac849ec1041031c769751b3d31c178
https://pubmed.ncbi.nlm.nih.gov/11719428
https://pubmed.ncbi.nlm.nih.gov/11719428
Autor:
T R, Rebbeck, Y, Wang, P W, Kantoff, K, Krithivas, S L, Neuhausen, A K, Godwin, M B, Daly, S A, Narod, J S, Brunet, D, Vesprini, J E, Garber, H T, Lynch, B L, Weber, M, Brown
Publikováno v:
Cancer research. 61(14)
Women who have inherited a germ-line mutation in the BRCA1 or BRCA2 (BRCA1/2) genes have a greatly increased risk of developing breast cancer compared with the general population. However, there is also substantial interindividual variability in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::44238e0716db1062633b0e380d71f542
https://pubmed.ncbi.nlm.nih.gov/11454686
https://pubmed.ncbi.nlm.nih.gov/11454686
Publikováno v:
Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 10(2)
Germ-line p53 mutations are associated with dominantly inherited Li-Fraumeni syndrome (LFS), which features early-onset sarcomas of bone and soft tissues, carcinomas of the breast and adrenal cortex, brain tumors, and acute leukemias. However, carrie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9ea4032ea0c70fa0a1af47afa22aca4
https://pubmed.ncbi.nlm.nih.gov/11219776
https://pubmed.ncbi.nlm.nih.gov/11219776
Autor:
A H, Partridge, J E, Garber
Publikováno v:
Seminars in oncology. 27(6)
The long-term outcomes of children exposed to antineoplastic agents in utero are not well-defined. Existing data are significantly limited by small numbers, heterogeneous patient populations and regimens, brief and unsystematic assessments in follow-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2edae3d503285d63aa0442b1f438c5c9
https://pubmed.ncbi.nlm.nih.gov/11130479
https://pubmed.ncbi.nlm.nih.gov/11130479
Autor:
S, Syngal, D, Schrag, M, Falchuk, N, Tung, F A, Farraye, D, Chung, M, Wright, A, Whetsell, G, Miller, J E, Garber
Publikováno v:
JAMA. 284(7)
The I1307K mutation of the APC gene is found in approximately 6% of the Ashkenazi Jewish population and is associated with elevated risk of colorectal cancer. The incidence of the mutation in patients with colorectal adenomas is unknown.To determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::37168e6758875046c0a535cb50de73bf
https://pubmed.ncbi.nlm.nih.gov/10938175
https://pubmed.ncbi.nlm.nih.gov/10938175
Autor:
E M, Rohlfs, N, Puget, M L, Graham, B L, Weber, J E, Garber, C, Skrzynia, J L, Halperin, G M, Lenoir, L M, Silverman, S, Mazoyer
Publikováno v:
Genes, chromosomescancer. 28(3)
Constitutive large deletions and duplications of BRCA1 resulting from Alu-mediated recombination account for a significant proportion of disease-causing mutations in breast and/or ovarian cancer families. Using Southern blot analysis and a protein tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dbb5fbe39345410ebbcca1da977fc3c5
https://pubmed.ncbi.nlm.nih.gov/10862036
https://pubmed.ncbi.nlm.nih.gov/10862036
Publikováno v:
Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 9(1)
Considerable research attention has been given to the impact of genetic testing on psychological outcomes. Participation in genetic testing also may impact on health behaviors that increase the risk of cancer and other chronic diseases. The purpose o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb5961cc19ae044a4ca60d4de9373c31
https://pubmed.ncbi.nlm.nih.gov/10667468
https://pubmed.ncbi.nlm.nih.gov/10667468
Publikováno v:
JAMA. 283(5)
Women with BRCA1- or BRCA2-associated breast cancer are at increased risk for contralateral breast cancer and ovarian cancer and therefore may consider secondary cancer prevention strategies, such as prophylactic surgery and tamoxifen therapy. It is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22fcebb155f70693931f853f93e784fa
https://pubmed.ncbi.nlm.nih.gov/10865296
https://pubmed.ncbi.nlm.nih.gov/10865296
Autor:
R D, Kolodner, J D, Tytell, J L, Schmeits, M F, Kane, R D, Gupta, J, Weger, S, Wahlberg, E A, Fox, D, Peel, A, Ziogas, J E, Garber, S, Syngal, H, Anton-Culver, F P, Li
Publikováno v:
Cancer research. 59(20)
Hereditary nonpolyposis colorectal carcinoma (HNPCC) is due primarily to inherited mutations in two mismatch repair genes, MSH2 and MLH1, whereas germ-line mutations in other mismatch repair genes are rare. We examined the frequency of germ-line msh6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::374f3d054f044c8490fb88f8b114bc40
https://pubmed.ncbi.nlm.nih.gov/10537275
https://pubmed.ncbi.nlm.nih.gov/10537275