Zobrazeno 1 - 10
of 272
pro vyhledávání: '"Jane F. Lynch"'
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Table 1 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03a312ce5bd2554b5b8aa100e29f6b73
https://doi.org/10.1158/0008-5472.22370685.v1
https://doi.org/10.1158/0008-5472.22370685.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Figure 1 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e21b3ce9f79af67b38f086b2d56f94f
https://doi.org/10.1158/0008-5472.22370688.v1
https://doi.org/10.1158/0008-5472.22370688.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Table 2 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f35983558639f12401ff99760e775b25
https://doi.org/10.1158/0008-5472.22370682.v1
https://doi.org/10.1158/0008-5472.22370682.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Large germline deletions within the mismatch repair gene MSH2 account for a significant proportion (up to 20%) of all deleterious mutations of this gene which are associated with Lynch syndrome. An exons 1 to 6 deletion of MSH2, originally reported i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c191f3329d9a72241f6091604193cc13
https://doi.org/10.1158/0008-5472.c.6496491.v1
https://doi.org/10.1158/0008-5472.c.6496491.v1
Publikováno v:
Hereditary Malignant Melanoma ISBN: 9780429276514
Hereditary Malignant Melanoma
Hereditary Malignant Melanoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a59099cce7ee1e20402eec7db5ebf328
https://doi.org/10.1201/9780429276514-1
https://doi.org/10.1201/9780429276514-1
Autor:
Henry T. Lynch, Jane F. Lynch
Publikováno v:
Vitamins and Minerals in the Prevention and Treatment of Cancer ISBN: 9781351077590
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ead3aaf4aa0e4fcafe07cf55f5a5beee
https://doi.org/10.1201/9781351077590-1
https://doi.org/10.1201/9781351077590-1
Thanks to the veritably logarithmic advances in the molecular genetics of many emerging hereditary cancer syndromes, genetic counselling has become of paramount importance. It is a key element of the emerging concepts for patient education and manage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e049c5dba26e1418b6955b859497fe4e
https://doi.org/10.1093/med/9780199656103.003.0031
https://doi.org/10.1093/med/9780199656103.003.0031
Autor:
Jane F. Lynch, Henry T. Lynch
Publikováno v:
Women's Health. 7:413-416
Evaluation of: Luo J, Margolis KL, Wactawski-Wende J et al. Association of active and passive smoking with risk of breast cancer among postmenopausal women: a prospective cohort study. BMJ DOI: 10.1136/bmj.d1016 (2011) (Epub ahead of print). Luo et a
Publikováno v:
Viszeralmedizin. 27:266-273
It is estimated that approximately 3–5% of all colorectal cancers may manifest the Lynch syndrome while its familial adenomatous polyposis counterpart accounts for less than 1% of the total colorectal cancer burden. Familial aggregation constitutes
Publikováno v:
Cancers
Cancers, Vol 2, Iss 4, Pp 1861-1883 (2010)
Cancers, Vol 2, Iss 4, Pp 1861-1883 (2010)
Pancreatic cancer’s high mortality rate equates closely with its incidence, thereby showing the need for development of biomarkers of its increased risk and a better understanding of its genetics, so that high-risk patients can be better targeted f