نتایج جستجو برای: familial cancer

تعداد نتایج: 958449  

Journal: :Japanese journal of clinical oncology 2015
Tatsuro Yamaguchi Yoichi Furukawa Yusuke Nakamura Nagahide Matsubara Hideki Ishikawa Masami Arai Naohiro Tomita Kazuo Tamura Kokichi Sugano Chikashi Ishioka Teruhiko Yoshida Yoshihiro Moriya Hideyuki Ishida Toshiaki Watanabe Kenichi Sugihara

OBJECTIVE The characteristics of familial colorectal cancer type X are poorly defined. Here we aimed to clarify the differences in clinical features between suspected familial colorectal cancer type X and Lynch syndrome in Japanese patients. METHODS We performed germline mutation analyses of mismatch repair genes in 125 patients. Patients who met the Amsterdam Criteria I but lacked mismatch r...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010
Pengyuan Liu Haris G Vikis Yan Lu Yian Wang Ann G Schwartz Susan M Pinney Ping Yang Mariza de Andrade Adi Gazdar Colette Gaba Diptasri Mandal Juwon Lee Elena Kupert Daniela Seminara John Minna Joan E Bailey-Wilson Christopher I Amos Marshall W Anderson Ming You

BACKGROUND Genetic factors play important roles in lung cancer susceptibility. In this study, we replicated the association of 5p15.33 and 6p21.33 with familial lung cancer. Taking into account the previously identified genetic susceptibility variants on 6q23-25/RGS17 and 15q24-25.1, we further determined the cumulative association of these four genetic regions and the population attributable r...

2006
Jacek Gronwald Andrzej Raczyński Mariusz Tarhoni Mirosław Blachowski Tomasz Huzarski Tomasz Byrski Aleksandra Tołoczko-Grabarek Tadeusz Dębniak Cezary Cybulski Jowita Huzarska Oleg Oszurek Jan Lubiński

The largest worldwide population screening for cancer family syndromes was initiated in January 2001 in the West Pomeranian Region of Poland with 1.7 m inhabitants. In the first step in the period January 2001 – May 2002 family doctors and nurses collected questionnaires asking about cancer family history among 1st and 2nd degree relatives from 1,258,401 of 1.5 m individuals (87%) who were insu...

Journal: :Jurnal Keperawatan Komprehensif : Comprehensive Nursing Journal 2022

Aims: To compare psychosocial status between familial and non-familial breast cancer patients. Methods: This study used a descriptive analytic design with cross-sectional approach. Population sampling were taken at Baladika Husada Hospital Jember total technique of 90 respondents. The inclusion criteria in this native Regency diagnosed since the end 2021, histologically documented diagnosis can...

Journal: :Saudi medical journal 2004
Manar F Atoum Huda M Al-Hourani

OBJECTIVE To compare the risk factors such as age, menopause, menarche, age at the first pregnancy, number of pregnancies and breast feeding period between the familial and non-familial breast cancer females in Jordan. METHODS This study was carried out in Al-Basheer Hospital, Amman, Jordan during the period 2000 and 2002. A questionnaire was used to collect information from 99 females who we...

اعتمادی, کتایون, مهدی پور, پروین,

          p53 gene is one of the most tumor suppressor genes that causes more    than 50 percent of the human cancers. Considering the daily rise in the    incidence of breast cancer in various parts of the world , including Iran ,    there was a great need for a molecular study for determination of P53    ...

Journal: :Postgraduate medical journal 1988
T Fukutomi R Inoue T Ushijima M Toyoda

Japanese breast cancer families were collected and classified into the following 7 types according to the onset age and the distribution of other cancers in the family lines; early-onset type, late-onset type, familial breast-ovarian cancer type, familial breast-prostate cancer type, familial breast-thyroid cancer type, familial male and female breast cancer type and multiple primary cancer typ...

2009
Kouji Banno Megumi Yanokura Yusuke Kobayashi Makiko Kawaguchi Hiroyuki Nomura Akira Hirasawa Nobuyuki Susumu Daisuke Aoki

Some cases of endometrial cancer are associated with a familial tumor and are referred to as hereditary nonpolyposis colorectal cancer (HNPCC or Lynch syndrome). Such tumors are thought to be induced by germline mutation of the DNA mismatch repair (MMR) gene, but many aspects of the pathology of familial endometrial cancer are unclear and no effective screening method has been established. Howe...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2012
Joan P Breyer T Grant Avritt Kate M McReynolds William D Dupont Jeffrey R Smith

BACKGROUND A recent study of familial and early onset prostate cancer reported a recurrent rare germline mutation of HOXB13 among men of European descent. The gene resides within the 17q21 hereditary prostate cancer linkage interval. METHODS We evaluated the G84E germline mutation (rs138213197) of HOXB13 in a case-control study of familial prostate cancer at Vanderbilt University (Nashville, ...

Journal: :Cancer discovery 2016
Nicholas J Roberts Alexis L Norris Gloria M Petersen Melissa L Bondy Randall Brand Steven Gallinger Robert C Kurtz Sara H Olson Anil K Rustgi Ann G Schwartz Elena Stoffel Sapna Syngal George Zogopoulos Syed Z Ali Jennifer Axilbund Kari G Chaffee Yun-Ching Chen Michele L Cote Erica J Childs Christopher Douville Fernando S Goes Joseph M Herman Christine Iacobuzio-Donahue Melissa Kramer Alvin Makohon-Moore Richard W McCombie K Wyatt McMahon Noushin Niknafs Jennifer Parla Mehdi Pirooznia James B Potash Andrew D Rhim Alyssa L Smith Yuxuan Wang Christopher L Wolfgang Laura D Wood Peter P Zandi Michael Goggins Rachel Karchin James R Eshleman Nickolas Papadopoulos Kenneth W Kinzler Bert Vogelstein Ralph H Hruban Alison P Klein

UNLABELLED Pancreatic cancer is projected to become the second leading cause of cancer-related death in the United States by 2020. A familial aggregation of pancreatic cancer has been established, but the cause of this aggregation in most families is unknown. To determine the genetic basis of susceptibility in these families, we sequenced the germline genomes of 638 patients with familial pancr...

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