Works matching Payne Stewart

Results: 20

THE IMPACT OF HOME SCHOOLING REGULATIONS ON EDUCATIONAL ENROLLMENTS IN THE UNITED STATES.

Published in:

Education, 2005, v. 126, n. 2, p. 353

By:

Stewart, Kima Payne;
Neeley, Richard A.

Publication type:

Article

Development of a denaturing high-performance liquid chromatography screening method for SMAD4 in juvenile polyposis syndrome.

Published in:

Annals of Clinical Biochemistry, 2007, v. 44, n. 2, p. 159, doi. 10.1258/000456307780118181

By:

Hatch, Sarah L.;
Trewick, Anne L.;
Payne, Stewart J.

Publication type:

Article

Female Germline Mosaicism in Tuberous Sclerosis Confirmed by Molecular Genetic Analysis.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 13, p. 2265, doi. 10.1093/hmg/6.13.2265

By:

Yates, John R.W.;
van Bakel, Inge;
Sepp, Tiina;
Payne, Stewart J.;
Webb, David W.;
Nevin, Norman C.;
Green, Andrew J.

Publication type:

Article

A Family with Stickler Syndrome Type 2 Has a Mutation in the COL11A1 Gene Resulting in the Substitution of Glycine 97 by Valine in a1(XI) Collagen.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 9, p. 1339, doi. 10.1093/hmg/5.9.1339

By:

Richards, Allan J.;
Yates, John R. W.;
Williams, Rebecca;
Payne, Stewart J.;
Michael Pope, F.;
Scott, John D.;
Snead, Martin P.

Publication type:

Article

Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 11, p. 2139

By:

Richards, Frances M.;
Payne, Stewart J.;
Zbar, Berton;
Affara, Nabeel A.;
Ferguson-Smith, Malcolm A.;
Maher, Eamonn R.

Publication type:

Article

Molecular genetic analysis of the 3p — syndrome.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 6, p. 903

By:

Phipps, Maude E.;
Latif, Farida;
Prowse, Amanda;
Payne, Stewart J.;
Dietz-Band, Jeanne;
Leversha, Margaret;
Affara, Nabeel A.;
Moore, Anthony T.;
Tolmie, John;
Schinzel, Albert;
Lerman, Michael I.;
Ferguson-Smith, Malcolm A.;
Maher, Eamonn R.

Publication type:

Article

Direct, non-radioactive detection of mutations in Multiple Endocrine Neoplasia Type 2A families.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 4, p. 643

By:

McMahon, Robert;
Mulligan, Lois M.;
Healey, Catherine S.;
Payne, Stewart J.;
Ponder, Margaret;
Ferguson-Smith, Malcolm A.;
Barton, David E.;
J.Ponder, Bruce A.

Publication type:

Article

The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis.

Published in:

Nature Medicine, 1999, v. 5, n. 9, p. 1071, doi. 10.1038/12511

By:

Lamlum, Hanan;
Ilyas, Mohammad;
Rowan, Andrew;
Clark, Susan;
Johnson, Victoria;
Bell, Jennie;
Frayling, Ian;
Efstathiou, Jason;
Pack, Kevin;
Payne, Stewart;
Roylance, Rebecca;
Gorman, Patricia;
Sheer, Denise;
Neale, Kay;
Phillips, Robin;
Talbot, Ian;
Bodmer, Walter;
Tomlinson, Ian

Publication type:

Article

Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.

Published in:

Human Mutation, 2000, v. 15, n. 1, p. 120, doi. 10.1002/(SICI)1098-1004(200001)15:1<120::AID-HUMU32>3.0.CO;2-B

By:

Bradbury, Rachel;
Fagan, Elizabeth;
Payne, Stewart J.

Publication type:

Article

A novel missense mutation S65C in the HFE gene with a possible role in hereditary haemochromatosis.

Published in:

Human Mutation, 1999, v. 13, n. 6, p. 507, doi. 10.1002/(SICI)1098-1004(1999)13:6<507::AID-HUMU25>3.0.CO;2-X

By:

Fagan, Elizabeth;
Payne, Stewart J.

Publication type:

Article

Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 509, doi. 10.1007/s10689-012-9544-4

By:

Farrell, Michael;
Hughes, David;
Berry, Ian;
Gallagher, David;
Glogowski, Emily;
Payne, Stewart;
Kennedy, Michael;
Clarke, Róisín;
White, Susan;
Muldoon, Cian;
Macdonald, Fiona;
Rehal, Pauline;
Crompton, Danielle;
Roring, Solvig;
Duke, Sarah;
McDevitt, Trudi;
Barton, David;
Hodgson, Shirley;
Green, Andrew;
Daly, Peter

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

An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation.

Published in:

Familial Cancer, 2007, v. 6, n. 3, p. 317, doi. 10.1007/s10689-007-9119-y

By:

Angela Arnold;
Stewart Payne;
Samantha Fisher;
Diane Fricker;
Judith Soloway;
Susan White;
Marco Novelli;
Kylie MacDonald;
James Mackay;
Richard Groves;
Natalie Canham

Publication type:

Article

Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer.

Published in:

Oncogene, 2002, v. 21, n. 12, p. 1928, doi. 10.1038/sj.onc.1205245

By:

Porter, Timothy R.;
Richards, Frances M.;
Houlston, Richard S.;
Evans, D. Gareth R.;
Jankowski, Janusz A.;
Macdonald, Fiona;
Norbury, Gail;
Payne, Stewart J.;
Fisher, Samantha A.;
Tomlinson, Ian;
Maher, Eamonn R.

Publication type:

Article

Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems.

Published in:

American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 1192, doi. 10.1002/ajmg.a.33986

By:

de Smith, Adam J.;
van Haelst, Mieke M.;
Ellis, Richard J.;
Holder, Susan E.;
Payne, Stewart J.;
Hashim, Sugera K.;
Froguel, Philippe;
Blakemore, Alexandra I.F.

Publication type:

Article

Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome.

Published in:

European Child & Adolescent Psychiatry, 2003, v. 12, n. 4, p. 172, doi. 10.1007/s00787-003-0333-3

By:

Sabaratnam, Manga;
Murthy, Naga Venkatesha;
Wijeratne, Anusha;
Buckingham, Ann;
Payne, Stewart

Publication type:

Article

Women's Health.

Published in:

1998

By:

Massion, Charlea T.;
Meyer, Harriet S.;
Payne Epps, Roselyn;
Stewart, Susan C.

Publication type:

Book Review

Immediate affect as a basis for intuitive moral judgement: An adaptation of the affect misattribution procedure.

Published in:

Cognition & Emotion, 2010, v. 24, n. 3, p. 522, doi. 10.1080/02699930902847193

By:

Hofmann, Wilhelm;
Baumert, Anna

Publication type:

Article

Sir Wilfrid Laurier: The Weakling Who Stood His Ground.

Published in:

2006

By:

Hamilton, Gail

Publication type:

Book Review

Not Always Black and White: The Effect of Race and Emotional Expression on Implicit Attitudes.

Published in:

Social Cognition, 2018, v. 36, n. 5, p. 534, doi. 10.1521/soco.2018.36.5.534

By:

Steele, Jennifer R.;
George, Meghan;
Cease, Margaret K.;
Fabri, Tracy L.;
Schlosser, Jacob

Publication type:

Article