Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Katherine A, Schneider"'
Autor:
Kenneth P. Tercyak, Tiffani A. DeMarco, Katherine A. Schneider, George Luta, Claudine Isaacs, Judy E. Garber, Marcelo M. Sleiman, Jr., Mary Rose Yockel, Beth N. Peshkin
Publikováno v:
PEC Innovation, Vol 2, Iss , Pp 100129- (2023)
Objective: Evaluate the impact of a targeted family communication intervention for mothers undergoing genetic counseling and testing (GCT) for BRCA gene alterations. Methods: Following BRCA GCT, mothers (N = 204; M age = 45 y) were randomized to eith
Externí odkaz:
https://doaj.org/article/d15b4ed2a555415c8e476d3e54b7713c
Autor:
Whitney, Espinel, Marjan, Champine, Heather, Hampel, Joanne, Jeter, Kevin, Sweet, Robert, Pilarski, Rachel, Pearlman, Kate, Shane, Pamela, Brock, Judith A, Westman, Lindsay, Kipnis, Jilliane, Sotelo, Anu, Chittenden, Samantha, Culver, Jill E, Stopfer, Katherine A, Schneider, Rosalba, Sacca, Diane R, Koeller, Shraddha, Gaonkar, Erica, Vaccari, Sarah, Kane, Scott T, Michalski, Shan, Yang, Sarah M, Nielsen, Sara L, Bristow, Stephen E, Lincoln, Robert L, Nussbaum, Edward D, Esplin
Publikováno v:
Cancers. 14(10)
Consensus guidelines for hereditary breast and ovarian cancer include management recommendations for pathogenic/likely pathogenic (P/LP) variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24cf0bd64bd4582859098cbce772d872
https://pubmed.ncbi.nlm.nih.gov/35626031
https://pubmed.ncbi.nlm.nih.gov/35626031
Publikováno v:
Wood and Fiber Science. 52:292-297
Two figured woods, commonly known as birdseye maple ( Acer saccharum , sugar maple) and curly maple ( Acer rubrum , red maple), were exposed to brown rot and white rot fungi in a standard laboratory decay test and compared with unfigured wood of each
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1b535024c6416fb5dc11d6ddbd57d15
https://doi.org/10.22382/wfs-2020-027
https://doi.org/10.22382/wfs-2020-027
Publikováno v:
The Hereditary Basis of Childhood Cancer ISBN: 9783030744465
Genetic testing options are now widely available to pediatric cancer patients and their families. Thus, it is important for clinicians to become familiar with the features and patterns of hereditary cancers, the elements of the genetic testing proces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::711c0a8a5143c692a91e16a8e18d2c45
https://doi.org/10.1007/978-3-030-74448-9_14
https://doi.org/10.1007/978-3-030-74448-9_14
Counseling About Cancer A key resource for all genetic counselors and other healthcare providers, this comprehensive reference has been completely updated and reorganized for its fourth edition Over 50 hereditary cancer predisposition genes have now
Autor:
Miguel Navarro, Quillon J. Simpson, Travis J. DeLano, Maria Santos Martinez-Martinez, Raquel García-Hernández, Rosario Diaz-Gonzalez, Westley Tear, Guiomar Pérez-Moreno, William G. Devine, Lori Ferrins, Dolores González-Pacanowska, Luis M. Ruiz-Pérez, Melanie G. Fritsche, Katherine M. Schneider, Michael P. Pollastri, Francisco Gamarro, John K. Fisher, Cristina Bosch-Navarrete, Pilar Manzano-Chinchon, Vivian Hilborne, Dana M. Klug, Raeann M. Dalton, Gloria Ceballos-Pérez, Eftychia M. Mavrogiannaki, Melissa J. Buskes
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
RSC Med Chem
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
RSC Med Chem
Human African trypanosomiasis is a neglected tropical disease (NTD) that is fatal if left untreated. Although approximately 13 million people live in moderate- to high-risk areas for infection, current treatments are plagued by problems with safety,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c419df9071d8f28b3bdefbdbcc538de7
http://hdl.handle.net/10261/246477
http://hdl.handle.net/10261/246477
Objective To evaluate the long-term efficacy and safety of canakinumab and explore prediction of response in patients with systemic juvenile idiopathic arthritis (JIA) with or without fever at treatment initiation. Methods At enrollment, patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::07a3ecf7f1671a36828141f2f103f696
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3193110
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3193110
Autor:
Katherine A. Schneider, Rose B. McGee, Maria Isabel Achatz, Laurence Brugières, Kris Ann P. Schultz, Surya P. Rednam, Junne Kamihara, Jonathan D. Wasserman, William D. Foulkes, Harriet Druker, Lisa Diller, Leslie Doros
Publikováno v:
Clinical Cancer Research. 23:e76-e82
PTEN hamartoma tumor syndrome (PHTS), DICER1 syndrome, and hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome are pleiotropic tumor predisposition syndromes that include benign and malignant neoplasms affecting adults and children. PHTS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fd9dbb346cea23a21b155fbd5cc190e
https://doi.org/10.1158/1078-0432.ccr-17-0629
https://doi.org/10.1158/1078-0432.ccr-17-0629
Autor:
Louise C. Strong, Joshua D. Schiffman, Kenan Onel, Laurence Brugières, Christian P. Kratz, Jordan R. Hansford, Judy Garber, Rose B. McGee, D. Gareth Evans, Anita Villani, David Malkin, Sharon A. Savage, Maria Isabel Achatz, Charles G. Mullighan, Stefan M. Pfister, Thierry Frebourg, Katherine A. Schneider, Jonathan D. Wasserman, Kristian W. Pajtler, Katherine A. Janeway, Wendy Kohlmann, Mary Louise C. Greer
Publikováno v:
Kratz, C P, Achatz, M I, Brugières, L, Frebourg, T, Garber, J E, Greer, M-L C, Hansford, J R, Janeway, K A, Kohlmann, W K, McGee, R, Mullighan, C G, Onel, K, Pajtler, K W, Pfister, S M, Savage, S A, Schiffmann, J, Schneider, K, Strong, L C, Evans, D, Wasserman, J, Villani, A & Malkin, D 2017, ' Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome ', Clinical Cancer Research, vol. 23, no. 11, pp. e38-e45 . https://doi.org/10.1158/1078-0432.CCR-17-0408
Li-Fraumeni syndrome (LFS) is an autosomal dominantly inherited condition caused by germline mutations of the TP53 tumor suppressor gene encoding p53, a transcription factor triggered as a protective cellular mechanism against different stressors. Lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d156f51366db8e13facc58b6a1a7e9c
https://doi.org/10.1158/1078-0432.ccr-17-0408
https://doi.org/10.1158/1078-0432.ccr-17-0408