Works matching IS 13899600 AND DT 2008 AND VI 7

Results: 51

The three nucleotide deletion within the 3′untranslated region of MLH1 resulting in gene expression reduction is not a causal alteration in Lynch syndrome.

Published in:

2008

By:

Tinat, J.;
Baert-Desurmont, S.;
Latouche, J.;
Vasseur, S.;
Martin, C.;
Bouvignies, E.;
Frébourg, T.

Publication type:

Letter

Pathology of the hereditary colorectal carcinoma.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 15, doi. 10.1007/s10689-007-9146-8

By:

Zoran Gatalica;
Emina Torlakovic

Publication type:

Article

Family history and colorectal cancer survival in women.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 287, doi. 10.1007/s10689-008-9190-z

By:

Kirchhoff, Anne;
Newcomb, Polly;
Trentham-Dietz, Amy;
Nichols, Hazel;
Hampton, John

Publication type:

Article

Screening for urinary tract cancer with urine cytology in Lynch syndrome and familial colorectal cancer.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 303, doi. 10.1007/s10689-008-9193-9

By:

Myrhøj, T.;
Andersen, M.-B.;
Bernstein, I.

Publication type:

Article

Delivering cancer genetics services-new ways of working.

Published in:

2008

By:

Eeles, Ros;
Purland, Glyn;
Maher, Jane;
Evans, D.

Publication type:

Correction Notice

Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 319, doi. 10.1007/s10689-008-9194-8

By:

Puijenbroek, Marjo;
Middeldorp, Anneke;
Tops, Carli;
Eijk, Ronald;
Klift, Heleen;
Vasen, Hans;
Wijnen, Juul;
Hes, Frederik;
Oosting, Jan;
Wezel, Tom;
Morreau, Hans

Publication type:

Article

Cascade genetic testing for mismatch repair gene mutations.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 293, doi. 10.1007/s10689-008-9192-x

By:

Mitchell, R.;
Ferguson, R.;
Macdonald, A.;
Dunlop, M.;
Campbell, H.;
Porteous, M.

Publication type:

Article

Mutation spectrum in HNPCC in the Israeli population.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 309, doi. 10.1007/s10689-008-9191-y

By:

Goldberg, Yael;
Porat, Rinnat;
Kedar, Inbal;
Shochat, Chen;
Sagi, Michal;
Eilat, Avital;
Mendelson, Suzan;
Hamburger, Tamar;
Nissan, Aviram;
Hubert, Ayala;
Kadouri, Luna;
Pikarski, Eli;
Lerer, Israela;
Abeliovich, Dvorah;
Bercovich, Dani;
Peretz, Tamar

Publication type:

Article

Predictors of choosing life-long screening or prophylactic surgery in women at high and moderate risk for breast and ovarian cancer.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 347, doi. 10.1007/s10689-008-9189-5

By:

Leeuw, J.;
Vliet, M.;
Ausems, M.

Publication type:

Article

Family history of cancer in Brazil: is it being used?

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 229, doi. 10.1007/s10689-008-9180-1

By:

Danilo Viana;
Juvenal Góes;
Cláudio Coy;
Maria de Lourdes Setsuko Ayrizono;
Carmen Lima;
Iscia Lopes-Cendes

Publication type:

Article

Muir-Torre Syndrome: expanding the genotype and phenotype—a further family with a MSH6 mutation.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 255, doi. 10.1007/s10689-008-9183-y

By:

H. Murphy;
R. Armstrong;
D. Cairns;
K. Greenhalgh

Publication type:

Article

Working through a diagnostic challenge: colonic polyposis, Amsterdam criteria, and a mismatch repair mutation.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 281, doi. 10.1007/s10689-007-9179-z

By:

Jasperson, Kory;
Blazer, Kathleen;
Lowstuter, Katrina;
Weitzel, Jeffrey

Publication type:

Article

Predicting breast cancer risk: implications of a “weak” family history.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 361, doi. 10.1007/s10689-008-9197-5

By:

Anderson, Elaine;
Berg, Jonathan;
Black, Roger;
Bradshaw, Nicola;
Campbell, Joyce;
Cetnarskyj, Roseanne;
Drummond, Sarah;
Davidson, Rosemarie;
Dunlop, Jacqueline;
Fordyce, Alison;
Gibbons, Barbara;
Goudie, David;
Gregory, Helen;
Hanning, Kirstie;
Holloway, Susan;
Longmuir, Mark;
McLeish, Lorna;
Murday, Vicky;
Miedzybrodska, Zosia;
Nicholson, Donna

Publication type:

Article

Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 331, doi. 10.1007/s10689-008-9195-7

By:

Magnusson, Susanne;
Borg, Åke;
Kristoffersson, Ulf;
Nilbert, Mef;
Wiebe, Thomas;
Olsson, Håkan

Publication type:

Article

Screen positive rates among six family history screening protocols for breast/ovarian cancer in four cohorts of women.

Published in:

Familial Cancer, 2008, v. 7, n. 4, p. 341, doi. 10.1007/s10689-008-9188-6

By:

McClain, Monica;
Palomaki, Glenn;
Hampel, Heather;
Westman, Judith;
Haddow, James

Publication type:

Article

Influence of germline polymorphisms of GSTT1 , GSTM1 , and GSTP1 in familial versus sporadic breast cancer susceptibility and survival.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 213, doi. 10.1007/s10689-007-9177-1

By:

Volga Syamala;
Leelakumari Sreeja;
Vani Syamala;
Praveenkumar Raveendran;
Rajan Balakrishnan;
Ratheesan Kuttan;
Ravindran Ankathil

Publication type:

Article

8th International Symposium on von Hippel-Lindau Disease.

Published in:: Familial Cancer, 2008, v. 7, p. S13, doi. 10.1007/s10689-008-9211-y
Publication type:: Article

The Inaugural Birt-Hogg-Dubé (BHD) Symposium.

Published in:: Familial Cancer, 2008, v. 7, p. S1, doi. 10.1007/s10689-008-9210-z
Publication type:: Article

Probability estimation models for prediction of BRCA1 and BRCA2 mutation carriers: COS compares favourably with other models.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 199

By:

Zosia Miedzybrodzka;
Neva Haites

Publication type:

Article

Prolactin and systemic malignancies: a close association.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 265, doi. 10.1007/s10689-008-9185-9

By:

Shailendra Kapoor

Publication type:

Article

Sebaceous adenomas in an MYH associated polyposis patient of Indian (Gujarati) origin.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 187, doi. 10.1007/s10689-007-9161-9

By:

Vadakke Ajith Kumar;
June Gold;
Eleanor Mallon;
Shyamala Thomas;
Shirley Hodgson

Publication type:

Article

Psychological and cancer-specific distress at 18 months post-testing in women with demonstrated BRCA1 mutations for hereditary breast/ovarian cancer.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 245

By:

Pål Møller;
Ketil Heimdal;
Alv Dahl

Publication type:

Article

Inequality of use of Cancer Genetics Services by members of breast, ovarian and colorectal cancer families in South East Scotland.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 259, doi. 10.1007/s10689-008-9184-x

By:

Susan Holloway;
Birgitta Bernhard;
Harry Campbell;
Roseanne Cetnarskyj;
Wayne Lam

Publication type:

Article

Use of association studies to define genetic modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 233, doi. 10.1007/s10689-008-9181-0

By:

David Hughes

Publication type:

Article

The extracolonic cancer spectrum in females with the common ‘South African’ hMLH1 c.C1528T mutation.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 191

By:

Paul Goldberg;
G. Pietersen;
Ursula Algar;
A. Vorster;
Dhiren Govender;
Raj Ramesar

Publication type:

Article

Prolactin levels, breast-feeding and milk production in a cohort of young healthy women from high-risk breast cancer families: implications for breast cancer risk.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 221, doi. 10.1007/s10689-007-9178-0

By:

Maria Hietala

Publication type:

Article

Tumor histology helps to identify Lynch syndrome among colorectal cancer patients.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 267, doi. 10.1007/s10689-008-9186-8

By:

Brindusa Truta;
Yunn-Yi Chen;
Amie Blanco;
Guoren Deng;
Peggy Conrad;
Yong Kim;
Eun Park;
Fernando Velayos;
Jonathan Terdiman

Publication type:

Article

Prevalence of BRCA1 and BRCA2 mutations in breast cancer patients from Cuba.

Published in:

Familial Cancer, 2008, v. 7, n. 3, p. 275, doi. 10.1007/s10689-008-9187-7

By:

Rolando Rodriguez;
Antonio Esperon;
Ramon Ropero;
Maria Rubio;
Ronald Rodriguez;
Rosa Ortiz;
Juan Anta;
Mario de los Rios;
Deyanira Carnesolta;
Maria del Olivera;
Somalia Vansam;
Robert Royer;
Mohammad Akbari;
Talia Donenberg;
Steven Narod

Publication type:

Article

Gonadal mosaicism and familial adenomatous polyposis.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 173, doi. 10.1007/s10689-007-9169-1

By:

Angela Schwab;
Thérèse Tuohy;
Michelle Condie

Publication type:

Article

Cancer risk reduction and reproductive concerns in female BRCA1/2 mutation carriers.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 179, doi. 10.1007/s10689-007-9171-7

By:

Ashley Staton;
Kristin Cobb;
Meredith Mills;
James Ford

Publication type:

Article

Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC).

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 163

By:

Peter Sasieni;
Richard Houlston;
Louise Izatt;
Ros Eeles;
Stewart Payne;
Samantha Fisher;
Shirley Hodgson

Publication type:

Article

Is MSH2 a breast cancer susceptibility gene?

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 151

By:

EE Wong;
Andrea Tesoriero;
Gulietta Pupo;
Margaret McCredie;
Graham Giles;
John Hopper;
Graham Mann;
David Goldgar

Publication type:

Article

Sessile serrated polyps of the colorectum are rare in patients with Lynch syndrome and in familial colorectal cancer families.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 157

By:

I. Bernstein;
S. Holck

Publication type:

Article

Loss of heterozygosity at 19p13.2 and 2q21 in tumours from familial clusters of non-medullary thyroid carcinoma.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 141

By:

Fernando Rodrigues;
Plamen Naidenov;
Paulo Figueiredo;
Beatriz Campos;
Manuela Lacerda

Publication type:

Article

BRCA1/2 mutation analysis in male breast cancer families from North West England.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 113, doi. 10.1007/s10689-007-9153-9

By:

D. Evans;
Mike Bulman;
Karen Young;
Emma Howard;
Stuart Bayliss;
Andrew Wallace;
Fiona Lalloo

Publication type:

Article

A novel MSH2 germline mutation in a Druze HNPCC family.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 135

By:

Renée Niessen;
Yael Laitman;
Dennie Rozeveld;
Robert Hofstra

Publication type:

Article

Characterization of the pathogenic mechanism of a novel BRCA2 variant in a Chinese family.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 125

By:

K. Chan;
U. Khoo;
J. Ford

Publication type:

Article

Familial breast cancer: double heterozygosity for BRCA1 and BRCA2 mutations with differing phenotypes.

Published in:

Familial Cancer, 2008, v. 7, n. 2, p. 119, doi. 10.1007/s10689-007-9154-8

By:

Margaret Smith;
Susan Fawcett;
Emanouil Sigalas;
Richard Bell;
Sophie Devery;
Nikolina Andrieska;
Ingrid Winship

Publication type:

Article

Standards of care in diagnosis and testing for hereditary colon cancer.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 65, doi. 10.1007/s10689-007-9159-3

By:

Lynch, Patrick M.

Publication type:

Article

Hereditary diffuse gastric cancer: association with lobular breast cancer.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 73

By:

Serena Masciari;
Niki Boyd;
Sara Wiyrick;
Pardeep Kaurah;
Janine Senz;
Wylie Burke;
Henry Lynch;
Judy Garber

Publication type:

Article

Hereditary colorectal cancer syndromes: molecular genetics, genetic counseling, diagnosis and management.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 27, doi. 10.1007/s10689-007-9165-5

By:

Henry Lynch;
Jane Lynch;
Patrick Lynch

Publication type:

Article

Pancreatic cancer and the FAMMM syndrome.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 103, doi. 10.1007/s10689-007-9166-4

By:

Henry Lynch;
Ramon Fusaro;
Jane Lynch

Publication type:

Article

A hereditary cancer syndrome seminar: perspective of a Continuing Medical Education (CME) Director.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 3, doi. 10.1007/s10689-007-9170-8

By:

Sally OâNeill

Publication type:

Article

Genetic counseling and clinical management of newly diagnosed breast cancer patients at genetic risk for BRCA germline mutations: perspective of a surgical oncologist.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 91, doi. 10.1007/s10689-007-9167-3

By:

Edibaldo Silva

Publication type:

Article

Foreword.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 1, doi. 10.1007/s10689-007-9168-2

By:

Henry Lynch

Publication type:

Article

Chemoprevention with special reference to inherited colorectal cancer.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 59, doi. 10.1007/s10689-007-9158-4

By:

Patrick Lynch

Publication type:

Article

Hereditary neoplasia syndromes and the role of the surgeon.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 97, doi. 10.1007/s10689-007-9156-6

By:

Lisa Coviello;
Robert Wascher

Publication type:

Article

Hereditary gynecologic cancers: differential diagnosis, surveillance, management and surgical prophylaxis.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 53, doi. 10.1007/s10689-007-9144-x

By:

Karen Lu

Publication type:

Article

The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch Syndrome: from bench to bedside.

Published in:

Familial Cancer, 2008, v. 7, n. 1, p. 41, doi. 10.1007/s10689-007-9145-9

By:

C. Boland;
Minoru Koi;
Dong Chang;
John Carethers

Publication type:

Article

Hereditary breast cancer: pathobiology, clinical translation, and potential for targeted cancer therapeutics.

Published in:: Familial Cancer, 2008, v. 7, n. 1, p. 83, doi. 10.1007/s10689-007-9147-7
Publication type:: Article