Chanock SJ - Search Results

1

Genetic variation in telomeric repeat binding factors 1 and 2 in aplastic anemia.

Savage SA, Calado RT, Xin ZT, Ly H, Young NS, Chanock SJ. Savage SA, et al. Among authors: chanock sj. Exp Hematol. 2006 May;34(5):664-71. doi: 10.1016/j.exphem.2006.02.008. Exp Hematol. 2006. PMID: 16647572 Free article.

2

Partial reconstitution of the respiratory burst oxidase in lymphoblastoid B cell lines lacking p67-phox after transfection with an expression vector containing wild-type and mutant p67 -phox cDNAs: Deletions of the carboxy and amino terminal residues of p67-phox are not required for activity.

Chanock SJ, Faust LR, Barrett D, Christensen B, Newburger PE, Babior BM. Chanock SJ, et al. Exp Hematol. 1996 Mar;24(4):531-6. Exp Hematol. 1996. PMID: 8608803

3

Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes.

Vázquez N, Lehrnbecher T, Chen R, Christensen BL, Gallin JI, Malech H, Holland S, Zhu S, Chanock SJ. Vázquez N, et al. Among authors: chanock sj. Exp Hematol. 2001 Feb;29(2):234-43. doi: 10.1016/s0301-472x(00)00646-9. Exp Hematol. 2001. PMID: 11166463 Free article.

4

Patterns of low-affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease.

Taylor JG, Tang D, Foster CB, Serjeant GR, Rodgers GP, Chanock SJ. Taylor JG, et al. Among authors: chanock sj. Am J Hematol. 2002 Feb;69(2):109-14. doi: 10.1002/ajh.10048. Am J Hematol. 2002. PMID: 11835346 Free article.

5

Using genetic variation to study immunomodulation.

Chanock S, Taylor JG 6th. Chanock S, et al. Curr Opin Pharmacol. 2002 Aug;2(4):463-9. doi: 10.1016/s1471-4892(02)00186-8. Curr Opin Pharmacol. 2002. PMID: 12127882 Review.

6

Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease.

Taylor JG 6th, Tang DC, Savage SA, Leitman SF, Heller SI, Serjeant GR, Rodgers GP, Chanock SJ. Taylor JG 6th, et al. Among authors: chanock sj. Blood. 2002 Dec 15;100(13):4303-9. doi: 10.1182/blood-2001-12-0306. Epub 2002 Aug 15. Blood. 2002. PMID: 12393616 Free article.

7

Genetic variation and hematopoietic stem cell transplantation: expansion of the paradigm.

Savage SA, Chanock S. Savage SA, et al. Pediatr Transplant. 2003;7 Suppl 3:32-9. doi: 10.1034/j.1399-3046.7.s3.4.x. Pediatr Transplant. 2003. PMID: 12603690

8

Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome.

Yamaguchi H, Baerlocher GM, Lansdorp PM, Chanock SJ, Nunez O, Sloand E, Young NS. Yamaguchi H, et al. Among authors: chanock sj. Blood. 2003 Aug 1;102(3):916-8. doi: 10.1182/blood-2003-01-0335. Epub 2003 Apr 3. Blood. 2003. PMID: 12676774 Free article.

9

Genetic variation and hematology: single-nucleotide polymorphisms, haplotypes, and complex disease.

Chanock S. Chanock S. Semin Hematol. 2003 Oct;40(4):321-8. doi: 10.1016/s0037-1963(03)00198-7. Semin Hematol. 2003. PMID: 14582082 Review.

10

Using germ-line genetic variation to investigate and treat cancer.

Savage SA, Chanock SJ. Savage SA, et al. Among authors: chanock sj. Drug Discov Today. 2004 Jul 15;9(14):610-8. doi: 10.1016/S1359-6446(04)03179-4. Drug Discov Today. 2004. PMID: 15239980 Review.

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