Haber D - Search Results

1

Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms.

Grundy P, Telzerow P, Paterson MC, Haber D, Berman B, Li F, Garber J. Grundy P, et al. Among authors: haber d. Lancet. 1991 Oct 26;338(8774):1079-80. doi: 10.1016/0140-6736(91)91937-p. Lancet. 1991. PMID: 1681381 No abstract available.

2

Genetic events in the development of Wilms' tumor.

Coppes MJ, Haber DA, Grundy PE. Coppes MJ, et al. Among authors: haber da. N Engl J Med. 1994 Sep 1;331(9):586-90. doi: 10.1056/NEJM199409013310906. N Engl J Med. 1994. PMID: 8047084 Review. No abstract available.

3

Molecular genetics of Wilms tumor.

Grundy P, Coppes MJ, Haber D. Grundy P, et al. Among authors: haber d. Hematol Oncol Clin North Am. 1995 Dec;9(6):1201-15. Hematol Oncol Clin North Am. 1995. PMID: 8591961

4

Prevalence and functional analysis of sequence variants in the ATR checkpoint mediator Claspin.

Zhang J, Song YH, Brannigan BW, Wahrer DC, Schiripo TA, Harris PL, Haserlat SM, Ulkus LE, Shannon KM, Garber JE, Freedman ML, Henderson BE, Zou L, Sgroi DC, Haber DA, Bell DW. Zhang J, et al. Mol Cancer Res. 2009 Sep;7(9):1510-6. doi: 10.1158/1541-7786.MCR-09-0033. Epub 2009 Sep 8. Mol Cancer Res. 2009. PMID: 19737971 Free PMC article.

5

Frequent met oncogene amplification in a Brca1/Trp53 mouse model of mammary tumorigenesis.

Smolen GA, Muir B, Mohapatra G, Barmettler A, Kim WJ, Rivera MN, Haserlat SM, Okimoto RA, Kwak E, Dahiya S, Garber JE, Bell DW, Sgroi DC, Chin L, Deng CX, Haber DA. Smolen GA, et al. Cancer Res. 2006 Apr 1;66(7):3452-5. doi: 10.1158/0008-5472.CAN-05-4181. Cancer Res. 2006. PMID: 16585167

6

Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.

Bell DW, Kim SH, Godwin AK, Schiripo TA, Harris PL, Haserlat SM, Wahrer DC, Haiman CA, Daly MB, Niendorf KB, Smith MR, Sgroi DC, Garber JE, Olopade OI, Le Marchand L, Henderson BE, Altshuler D, Haber DA, Freedman ML. Bell DW, et al. Among authors: haber da. Int J Cancer. 2007 Dec 15;121(12):2661-7. doi: 10.1002/ijc.23026. Int J Cancer. 2007. PMID: 17721994 Free PMC article.

7

An X chromosome gene, WTX, is commonly inactivated in Wilms tumor.

Rivera MN, Kim WJ, Wells J, Driscoll DR, Brannigan BW, Han M, Kim JC, Feinberg AP, Gerald WL, Vargas SO, Chin L, Iafrate AJ, Bell DW, Haber DA. Rivera MN, et al. Science. 2007 Feb 2;315(5812):642-5. doi: 10.1126/science.1137509. Epub 2007 Jan 4. Science. 2007. PMID: 17204608

8

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 28-2003. A 51-year-old premenopausal woman with newly diagnosed breast cancer and a strong family history of breast cancer.

Ryan PD, Haber DA, Shannon KM, Smith BL, Fan MJ. Ryan PD, et al. Among authors: haber da. N Engl J Med. 2003 Sep 11;349(11):1076-82. doi: 10.1056/NEJMcpc030018. N Engl J Med. 2003. PMID: 12968092 No abstract available.

9

The T790M "gatekeeper" mutation in EGFR mediates resistance to low concentrations of an irreversible EGFR inhibitor.

Godin-Heymann N, Ulkus L, Brannigan BW, McDermott U, Lamb J, Maheswaran S, Settleman J, Haber DA. Godin-Heymann N, et al. Mol Cancer Ther. 2008 Apr;7(4):874-9. doi: 10.1158/1535-7163.MCT-07-2387. Mol Cancer Ther. 2008. PMID: 18413800

10

Prophylactic oophorectomy to reduce the risk of ovarian and breast cancer in carriers of BRCA mutations.

Haber D. Haber D. N Engl J Med. 2002 May 23;346(21):1660-2. doi: 10.1056/NEJMed020044. Epub 2002 May 20. N Engl J Med. 2002. PMID: 12024000 No abstract available.

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