Mathew C - Search Results

1

Identification of missense and truncating mutations in the BRCA1 gene in sporadic and familial breast and ovarian cancer.

Greenman J, Mohammed S, Ellis D, Watts S, Scott G, Izatt L, Barnes D, Solomon E, Hodgson S, Mathew C. Greenman J, et al. Among authors: mathew c. Genes Chromosomes Cancer. 1998 Mar;21(3):244-9. Genes Chromosomes Cancer. 1998. PMID: 9523200

2

Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer.

Izatt L, Greenman J, Hodgson S, Ellis D, Watts S, Scott G, Jacobs C, Liebmann R, Zvelebil MJ, Mathew C, Solomon E. Izatt L, et al. Among authors: mathew c. Genes Chromosomes Cancer. 1999 Dec;26(4):286-94. Genes Chromosomes Cancer. 1999. PMID: 10534763

3

Risk factors for detecting germline BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish women with breast or ovarian cancer.

Hodgson SV, Heap E, Cameron J, Ellis D, Mathew CG, Eeles RA, Solomon E, Lewis CM. Hodgson SV, et al. Among authors: mathew cg. J Med Genet. 1999 May;36(5):369-73. J Med Genet. 1999. PMID: 10353781 Free PMC article.

4

Loss of heterozygosity of the oestrogen receptor gene in breast cancer.

Iwase H, Greenman JM, Barnes DM, Bobrow L, Hodgson S, Mathew CG. Iwase H, et al. Among authors: mathew cg. Br J Cancer. 1995 Mar;71(3):448-50. doi: 10.1038/bjc.1995.91. Br J Cancer. 1995. PMID: 7880722 Free PMC article.

5

Breast cancer and BRCA1 mutations.

Mathew CG, Solomon E, Hodgson SV. Mathew CG, et al. N Engl J Med. 1996 May 2;334(18):1198; author reply 1200. N Engl J Med. 1996. PMID: 8602197 No abstract available.

6

Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease.

Olavesen MG, Hampe J, Mirza MM, Saiz R, Lewis CM, Bridger S, Teare D, Easton DF, Herrmann T, Scott G, Hirst J, Sanderson J, Hodgson SV, Lee J, MacPherson A, Schreiber S, Lennard-Jones JE, Curran ME, Mathew CG. Olavesen MG, et al. Among authors: mathew cg. Immunogenetics. 2000 Jan;51(1):1-7. doi: 10.1007/s002510050001. Immunogenetics. 2000. PMID: 10663555

7

Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family history.

Ellis D, Greenman J, Hodgson S, McCall S, Lalloo F, Cameron J, Izatt L, Scott G, Jacobs C, Watts S, Chorley W, Perrett C, Macdermot K, Mohammed S, Evans G, Mathew CG. Ellis D, et al. Among authors: mathew cg. J Med Genet. 2000 Oct;37(10):792-4. doi: 10.1136/jmg.37.10.792. J Med Genet. 2000. PMID: 11183185 Free PMC article. No abstract available.

8

Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia.

Tischkowitz MD, Morgan NV, Grimwade D, Eddy C, Ball S, Vorechovsky I, Langabeer S, Stöger R, Hodgson SV, Mathew CG. Tischkowitz MD, et al. Among authors: mathew cg. Leukemia. 2004 Mar;18(3):420-5. doi: 10.1038/sj.leu.2403280. Leukemia. 2004. PMID: 14749703

9

[Molecular analysis of the estrogen receptor (ER) gene in association with ER negativity in breast cancer].

Iwase H, Kobayashi S, Iwata H, Yamashita T, Ito K, Toyama T, Hara Y, Greenman J, Mathew CG. Iwase H, et al. Among authors: mathew cg. Gan To Kagaku Ryoho. 1996 Mar;23 Suppl 1:61-5. Gan To Kagaku Ryoho. 1996. PMID: 8702313 Review. Japanese.

10

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.

Faivre L, Guardiola P, Lewis C, Dokal I, Ebell W, Zatterale A, Altay C, Poole J, Stones D, Kwee ML, van Weel-Sipman M, Havenga C, Morgan N, de Winter J, Digweed M, Savoia A, Pronk J, de Ravel T, Jansen S, Joenje H, Gluckman E, Mathew CG. Faivre L, et al. Among authors: mathew cg. Blood. 2000 Dec 15;96(13):4064-70. Blood. 2000. PMID: 11110674 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

527 results

Search Page