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1.

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.

Tomlinson, Ian; Webb, Emily; Carvajal-Carmona, Luis; Broderick, Peter; Kemp, Zoe; Spain, Sarah; Penegar, Steven; Chandler, Ian; Gorman, Maggie; Wood, Wendy; Barclay, Ella; Lubbe, Steven; Martin, Lynn; Sellick, Gabrielle; Jaeger, Emma; Hubner, Richard; Wild, Ruth; Rowan, Andrew; Fielding, Sarah; Howarth, Kimberley; Silver, Andrew; Atkin, Wendy; Muir, Kenneth; Logan, Richard; Kerr, David; Johnstone, Elaine; Sieber, Oliver; Gray, Richard; Thomas, Huw; Peto, Julian; Cazier, Jean-Baptiste; Houlston, Richard.

Nat Genet; 39(8): 984-8, 2007 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-17618284

2.

Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency.

Almeida, Antonio M; Murakami, Yoshiko; Layton, D Mark; Hillmen, Peter; Sellick, Gabrielle S; Maeda, Yusuke; Richards, Stephen; Patterson, Scott; Kotsianidis, Ioannis; Mollica, Luigina; Crawford, Dorothy H; Baker, Alastair; Ferguson, Michael; Roberts, Irene; Houlston, Richard; Kinoshita, Taroh; Karadimitris, Anastasios.

Nat Med; 12(7): 846-51, 2006 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-16767100

3.

Mutations in PTF1A cause pancreatic and cerebellar agenesis.

Sellick, Gabrielle S; Barker, Karen T; Stolte-Dijkstra, Irene; Fleischmann, Christina; Coleman, Richard J; Garrett, Christine; Gloyn, Anna L; Edghill, Emma L; Hattersley, Andrew T; Wellauer, Peter K; Goodwin, Graham; Houlston, Richard S.

Nat Genet; 36(12): 1301-5, 2004 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-15543146

4.

Insight into the pathogenesis of chronic lymphocytic leukemia (CLL) through analysis of IgVH gene usage and mutation status in familial CLL.

Crowther-Swanepoel, Dalemari; Wild, Ruth; Sellick, Gabrielle; Dyer, Martin J S; Mauro, Francesca R; Cuthbert, Robert J G; Jonsson, Viggo; Matutes, Estella; Dearden, Claire; Wiley, James; Fuller, Stephen; Catovsky, Daniel; Houlston, Richard S.

Blood; 111(12): 5691-3, 2008 Jun 15.

Artículo en Inglés | MEDLINE | ID: mdl-18424666

5.

A novel DNA repair disorder with thrombocytopenia, nephrosis and features overlapping Cockayne syndrome.

Forsythe, Elizabeth; Wild, Ruth; Sellick, Gabrielle; Houlston, Richard S; Lehmann, Alan R; Wakeling, Emma.

Am J Med Genet A; 149A(10): 2075-9, 2009 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-19760648

6.

Deciphering the genetics of hereditary non-syndromic colorectal cancer.

Papaemmanuil, Eli; Carvajal-Carmona, Luis; Sellick, Gabrielle S; Kemp, Zoe; Webb, Emily; Spain, Sarah; Sullivan, Kate; Barclay, Ella; Lubbe, Steven; Jaeger, Emma; Vijayakrishnan, Jayaram; Broderick, Peter; Gorman, Maggie; Martin, Lynn; Lucassen, Anneke; Bishop, D Timothy; Evans, D Gareth; Maher, Eamonn R; Steinke, Verena; Rahner, Nils; Schackert, Hans K; Goecke, Timm O; Holinski-Feder, Elke; Propping, Peter; Van Wezel, Tom; Wijnen, Juul; Cazier, Jean-Baptiste; Thomas, Huw; Houlston, Richard S; Tomlinson, Ian.

Eur J Hum Genet; 16(12): 1477-86, 2008 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-18628789

7.

Analysis of a large multi-generational family provides insight into the genetics of chronic lymphocytic leukemia.

Fuller, Stephen J; Papaemmanuil, Elli; McKinnon, Leah; Webb, Emily; Sellick, Gabrielle S; Dao-Ung, Lan-Phuong; Skarratt, Kristen K; Crowther, Dalemari; Houlston, Richard S; Wiley, James S.

Br J Haematol; 142(2): 238-45, 2008 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-18503587

8.

Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk.

Bethke, Lara; Webb, Emily; Sellick, Gabrielle; Rudd, Matthew; Penegar, Stephen; Withey, Laura; Qureshi, Mobshra; Houlston, Richard.

BMC Cancer; 7: 123, 2007 Jul 05.

Artículo en Inglés | MEDLINE | ID: mdl-17615053

9.

Birth order pattern in the inheritance of chronic lymphocytic leukaemia and related lymphoproliferative disease.

Jønsson, Viggo; Tjønnfjord, Geir; Samuelsen, Sven Ove; Johannesen, Tom; Olsen, Jørgen; Sellick, Gabrielle; Houlston, Richard; Yuille, Martin; Catovsky, Daniel.

Leuk Lymphoma; 48(12): 2387-96, 2007 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-18067015

10.

Folate metabolism polymorphisms influence risk of colorectal adenoma recurrence.

Hubner, Richard A; Muir, Kenneth R; Liu, Jo-Fen; Sellick, Gabrielle S; Logan, Richard F A; Grainge, Matthew; Armitage, Nicholas; Chau, Ian; Houlston, Richard S.

Cancer Epidemiol Biomarkers Prev; 15(9): 1607-13, 2006 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-16985020

11.

Familial chronic lymphocytic leukemia.

Sellick, Gabrielle S; Catovsky, Daniel; Houlston, Richard S.

Semin Oncol; 33(2): 195-201, 2006 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-16616066

12.

Relationship between ARLTS1 polymorphisms and risk of chronic lymphocytic leukemia.

Sellick, Gabrielle S; Catovsky, Daniel; Houlston, Richard S.

Leuk Res; 30(12): 1573-6, 2006 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-16581122

13.

Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays.

Sellick, Gabrielle S; Longman, Cheryl; Tolmie, John; Newbury-Ecob, Ruth; Geenhalgh, Lynn; Hughes, Simon; Whiteford, Margo; Garrett, Christine; Houlston, Richard S.

Nucleic Acids Res; 32(20): e164, 2004 Nov 23.

Artículo en Inglés | MEDLINE | ID: mdl-15561999

14.

A form of autosomal dominant spondyloepiphyseal dysplasia is caused by a glycine to alanine substitution in the COL2A1 gene.

Sellick, Gabrielle S; Hoornaert, Kristein P; Mortier, Geert R; King, Catherine; Dolling, Claire L; Newbury-Ecob, Ruth A; Gargan, Martin; Hall, Christine M; Houlston, Richard S; Smithson, Sarah F.

Clin Dysmorphol; 15(4): 197-202, 2006 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-16957471

15.

A novel gene for neonatal diabetes maps to chromosome 10p12.1-p13.

Sellick, Gabrielle S; Garrett, Christine; Houlston, Richard S.

Diabetes; 52(10): 2636-8, 2003 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-14514650

16.

The predicted impact of coding single nucleotide polymorphisms database.

Rudd, Matthew F; Williams, Richard D; Webb, Emily L; Schmidt, Steffen; Sellick, Gabrielle S; Houlston, Richard S.

Cancer Epidemiol Biomarkers Prev; 14(11 Pt 1): 2598-604, 2005 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-16284384

17.

MTHFR polymorphisms and risk of chronic lymphocytic leukemia.

Rudd, Matthew F; Sellick, Gabrielle S; Allinson, Ruth; Matutes, Estella; Catovsky, Daniel; Houlston, Richard S.

Cancer Epidemiol Biomarkers Prev; 13(12): 2268-70, 2004 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-15598791

18.

The P2X7 receptor gene A1513C polymorphism does not contribute to risk of familial or sporadic chronic lymphocytic leukemia.

Sellick, Gabrielle S; Rudd, Matthew; Eve, Paul; Allinson, Ruth; Matutes, Estella; Catovsky, Daniel; Houlston, Richard S.

Cancer Epidemiol Biomarkers Prev; 13(6): 1065-7, 2004 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-15184265

19.

Familial cancer associated with a polymorphism in ARLTS1.

Sellick, Gabrielle S; Catovsky, Daniel; Houlston, Richard S.

N Engl J Med; 354(11): 1204-5; author reply 1204-5, 2006 Mar 16.

Artículo en Inglés | MEDLINE | ID: mdl-16540626

20.

Causation of chronic lymphocytic leukemia--insights from familial disease.

Houlston, Richard S; Sellick, Gabrielle; Yuille, Martin; Matutes, Estella; Catovsky, Daniel.

Leuk Res; 27(10): 871-6, 2003 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-12860003

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A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.

Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency.

Mutations in PTF1A cause pancreatic and cerebellar agenesis.

Insight into the pathogenesis of chronic lymphocytic leukemia (CLL) through analysis of IgVH gene usage and mutation status in familial CLL.

A novel DNA repair disorder with thrombocytopenia, nephrosis and features overlapping Cockayne syndrome.

Deciphering the genetics of hereditary non-syndromic colorectal cancer.

Analysis of a large multi-generational family provides insight into the genetics of chronic lymphocytic leukemia.

Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk.

Birth order pattern in the inheritance of chronic lymphocytic leukaemia and related lymphoproliferative disease.

Folate metabolism polymorphisms influence risk of colorectal adenoma recurrence.

Familial chronic lymphocytic leukemia.

Relationship between ARLTS1 polymorphisms and risk of chronic lymphocytic leukemia.

Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays.

A form of autosomal dominant spondyloepiphyseal dysplasia is caused by a glycine to alanine substitution in the COL2A1 gene.

A novel gene for neonatal diabetes maps to chromosome 10p12.1-p13.

The predicted impact of coding single nucleotide polymorphisms database.

MTHFR polymorphisms and risk of chronic lymphocytic leukemia.

The P2X7 receptor gene A1513C polymorphism does not contribute to risk of familial or sporadic chronic lymphocytic leukemia.

Familial cancer associated with a polymorphism in ARLTS1.

Causation of chronic lymphocytic leukemia--insights from familial disease.