Nichols K - Search Results

1

The EWS-WT1 translocation product induces PDGFA in desmoplastic small round-cell tumour.

Lee SB, Kolquist KA, Nichols K, Englert C, Maheswaran S, Ladanyi M, Gerald WL, Haber DA. Lee SB, et al. Among authors: nichols k. Nat Genet. 1997 Nov;17(3):309-13. doi: 10.1038/ng1197-309. Nat Genet. 1997. PMID: 9354795

2

WT1 induces expression of insulin-like growth factor 2 in Wilms' tumor cells.

Nichols KE, Re GG, Yan YX, Garvin AJ, Haber DA. Nichols KE, et al. Cancer Res. 1995 Oct 15;55(20):4540-3. Cancer Res. 1995. PMID: 7553624

3

Physical map and cosmid contig encompassing a new interstitial deletion of the X-linked lymphoproliferative syndrome region.

Lamartine J, Nichols KE, Yin L, Krainer M, Heitzmann F, Bernard A, Gaudi S, Lenoir GM, Sullivan JL, Ikeda JE, Porta G, Schlessinger D, Romeo G, Haber DA, Sylla BS, Harkin DP. Lamartine J, et al. Among authors: nichols ke. Eur J Hum Genet. 1996;4(6):342-51. doi: 10.1159/000472230. Eur J Hum Genet. 1996. PMID: 9043868

4

Childhood cancer predisposition: applications of molecular testing and future implications.

Nichols KE, Li FP, Haber DA, Diller L. Nichols KE, et al. J Pediatr. 1998 Mar;132(3 Pt 1):389-97. doi: 10.1016/s0022-3476(98)70007-1. J Pediatr. 1998. PMID: 9544888 Review. No abstract available.

5

Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome.

Nichols KE, Harkin DP, Levitz S, Krainer M, Kolquist KA, Genovese C, Bernard A, Ferguson M, Zuo L, Snyder E, Buckler AJ, Wise C, Ashley J, Lovett M, Valentine MB, Look AT, Gerald W, Housman DE, Haber DA. Nichols KE, et al. Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13765-70. doi: 10.1073/pnas.95.23.13765. Proc Natl Acad Sci U S A. 1998. PMID: 9811875 Free PMC article.

6

Heterozygous germline ATM mutations do not contribute to radiation-associated malignancies after Hodgkin's disease.

Nichols KE, Levitz S, Shannon KE, Wahrer DC, Bell DW, Chang G, Hegde S, Neuberg D, Shafman T, Tarbell NJ, Mauch P, Ishioka C, Haber DA, Diller L. Nichols KE, et al. J Clin Oncol. 1999 Apr;17(4):1259. doi: 10.1200/JCO.1999.17.4.1259. J Clin Oncol. 1999. PMID: 10561187

7

Prevalence of germline truncating mutations in ATM in women with a second breast cancer after radiation therapy for a contralateral tumor.

Shafman TD, Levitz S, Nixon AJ, Gibans LA, Nichols KE, Bell DW, Ishioka C, Isselbacher KJ, Gelman R, Garber J, Harris JR, Haber DA. Shafman TD, et al. Among authors: nichols ke. Genes Chromosomes Cancer. 2000 Feb;27(2):124-9. Genes Chromosomes Cancer. 2000. PMID: 10612799

8

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1.

Nichols KE, Crispino JD, Poncz M, White JG, Orkin SH, Maris JM, Weiss MJ. Nichols KE, et al. Nat Genet. 2000 Mar;24(3):266-70. doi: 10.1038/73480. Nat Genet. 2000. PMID: 10700180 Free PMC article.

9

Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene.

Arico M, Imashuku S, Clementi R, Hibi S, Teramura T, Danesino C, Haber DA, Nichols KE. Arico M, et al. Among authors: nichols ke. Blood. 2001 Feb 15;97(4):1131-3. doi: 10.1182/blood.v97.4.1131. Blood. 2001. PMID: 11159547 Free article.

10

Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome.

Lee SB, Kim SH, Bell DW, Wahrer DC, Schiripo TA, Jorczak MM, Sgroi DC, Garber JE, Li FP, Nichols KE, Varley JM, Godwin AK, Shannon KM, Harlow E, Haber DA. Lee SB, et al. Among authors: nichols ke. Cancer Res. 2001 Nov 15;61(22):8062-7. Cancer Res. 2001. PMID: 11719428

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