Mitri A - Search Results

1

A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome.

Perera S, Ramyar L, Mitri A, Pollett A, Gallinger S, Speevak MD, Aronson M, Bapat B. Perera S, et al. Among authors: mitri a. J Hum Genet. 2010 Jan;55(1):37-41. doi: 10.1038/jhg.2009.119. Epub 2009 Nov 13. J Hum Genet. 2010. PMID: 19911012

2

Genotype-phenotype correlations in attenuated adenomatous polyposis coli.

Soravia C, Berk T, Madlensky L, Mitri A, Cheng H, Gallinger S, Cohen Z, Bapat B. Soravia C, et al. Among authors: mitri a. Am J Hum Genet. 1998 Jun;62(6):1290-301. doi: 10.1086/301883. Am J Hum Genet. 1998. PMID: 9585611 Free PMC article.

3

Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer.

Bapat BV, Madlensky L, Temple LK, Hiruki T, Redston M, Baron DL, Xia L, Marcus VA, Soravia C, Mitri A, Shen W, Gryfe R, Berk T, Chodirker BN, Cohen Z, Gallinger S. Bapat BV, et al. Among authors: mitri a. Hum Genet. 1999 Feb;104(2):167-76. doi: 10.1007/s004390050931. Hum Genet. 1999. PMID: 10190329

4

Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium.

Millar AL, Pal T, Madlensky L, Sherman C, Temple L, Mitri A, Cheng H, Marcus V, Gallinger S, Redston M, Bapat B, Narod S. Millar AL, et al. Among authors: mitri a. Hum Mol Genet. 1999 May;8(5):823-9. doi: 10.1093/hmg/8.5.823. Hum Mol Genet. 1999. PMID: 10196371

5

MSH2 deficient mice are viable and susceptible to lymphoid tumours.

Reitmair AH, Schmits R, Ewel A, Bapat B, Redston M, Mitri A, Waterhouse P, Mittrücker HW, Wakeham A, Liu B, et al. Reitmair AH, et al. Among authors: mitri a. Nat Genet. 1995 Sep;11(1):64-70. doi: 10.1038/ng0995-64. Nat Genet. 1995. PMID: 7550317

6

Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP).

Bapat B, Berk T, Mitri A, Cohen Z, Gallinger S, Stern H. Bapat B, et al. Among authors: mitri a. Hum Mutat. 1994;4(4):253-6. doi: 10.1002/humu.1380040404. Hum Mutat. 1994. PMID: 7866403

7

Improved predictive carrier testing for familial adenomatous polyposis using DNA from a single archival specimen and polymorphic markers with multiple alleles.

Bapat B, Mitri A, Greenberg CR. Bapat B, et al. Among authors: mitri a. Hum Pathol. 1993 Dec;24(12):1376-9. doi: 10.1016/0046-8177(93)90274-k. Hum Pathol. 1993. PMID: 8276387

8

Identification of somatic APC gene mutations in periampullary adenomas in a patient with familial adenomatous polyposis (FAP).

Bapat B, Odze R, Mitri A, Berk T, Ward M, Gallinger S. Bapat B, et al. Among authors: mitri a. Hum Mol Genet. 1993 Nov;2(11):1957-9. doi: 10.1093/hmg/2.11.1957. Hum Mol Genet. 1993. PMID: 8281160 No abstract available.

9

A truncated hMSH2 transcript occurs as a common variant in the population: implications for genetic diagnosis.

Xia L, Shen W, Ritacca F, Mitri A, Madlensky L, Berk T, Cohen Z, Gallinger S, Bapat B. Xia L, et al. Among authors: mitri a. Cancer Res. 1996 May 15;56(10):2289-92. Cancer Res. 1996. PMID: 8625301

10

MSH2 deficiency contributes to accelerated APC-mediated intestinal tumorigenesis.

Reitmair AH, Cai JC, Bjerknes M, Redston M, Cheng H, Pind MT, Hay K, Mitri A, Bapat BV, Mak TW, Gallinger S. Reitmair AH, et al. Among authors: mitri a. Cancer Res. 1996 Jul 1;56(13):2922-6. Cancer Res. 1996. PMID: 8674041

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

26 results

Search Page

Filters