Cheng SH - Search Results

1

Alterations of RAS signalling in Chinese multiple myeloma patients: absent BRAF and rare RAS mutations, but frequent inactivation of RASSF1A by transcriptional silencing or expression of a non-functional variant transcript.

Ng MH, Lau KM, Wong WS, To KW, Cheng SH, Tsang KS, Chan NP, Kho BC, Lo KW, Tong JH, Lam CW, Chan JC. Ng MH, et al. Among authors: cheng sh. Br J Haematol. 2003 Nov;123(4):637-45. doi: 10.1046/j.1365-2141.2003.04664.x. Br J Haematol. 2003. PMID: 14616967 Free article.

2

Diagnosis of late onset neonatal sepsis with cytokines, adhesion molecule, and C-reactive protein in preterm very low birthweight infants.

Ng PC, Cheng SH, Chui KM, Fok TF, Wong MY, Wong W, Wong RP, Cheung KL. Ng PC, et al. Among authors: cheng sh. Arch Dis Child Fetal Neonatal Ed. 1997 Nov;77(3):F221-7. doi: 10.1136/fn.77.3.f221. Arch Dis Child Fetal Neonatal Ed. 1997. PMID: 9462194 Free PMC article. Clinical Trial.

3

Frequent death-associated protein kinase promoter hypermethylation in multiple myeloma.

Ng MH, To KW, Lo KW, Chan S, Tsang KS, Cheng SH, Ng HK. Ng MH, et al. Among authors: cheng sh. Clin Cancer Res. 2001 Jun;7(6):1724-9. Clin Cancer Res. 2001. PMID: 11410512

4

Recurrent chromosomal rearrangements involving breakpoints 3p21 and 19q13 in Chinese IgD multiple myeloma detected by G-banding and multicolor spectral karyotyping: a review of IgD karyotype literature.

Ng MH, Wong N, Tsang KS, Cheng SH, Chung YF, Lo KW. Ng MH, et al. Among authors: cheng sh. Hum Pathol. 2001 Sep;32(9):1016-20. doi: 10.1053/hupa.2001.27122. Hum Pathol. 2001. PMID: 11567234

5

Hereditary duplication of proximal chromosome 1q (q11q22) in a patient with T lymphoblastic lymphoma/leukaemia: a family study using G banding and comparative genomic hybridisation.

Chan NP, Ng MH, Cheng SH, Lee V, Tsang KS, Lau TT, Li CK. Chan NP, et al. Among authors: cheng sh. J Med Genet. 2002 Dec;39(12):e79. doi: 10.1136/jmg.39.12.e79. J Med Genet. 2002. PMID: 12471217 Free PMC article. No abstract available.

6

Chromosomal aberrations of multiple myeloma in Chinese patients at diagnosis: a study by combined G-banding and multicolor spectral karyotyping.

Ng MH, Wong N, Lau TT, Tsang KS, Cheng SH, Chan NP, Tang SH, Lei KI, Leung Y. Ng MH, et al. Among authors: cheng sh. Oncol Rep. 2003 May-Jun;10(3):587-91. Oncol Rep. 2003. PMID: 12684628

7

Establishment and characterization of a cytogenetically complex Chinese multiple myeloma-derived cell line with homozygous p53 deletion and cyclin E overexpression.

Cheng SH, Ng MH, Tsang KS, Lau KM, Chan JC, Liu HS, Chu RW, Poon CS, Ng HK. Cheng SH, et al. Int J Oncol. 2004 May;24(5):1141-8. Int J Oncol. 2004. PMID: 15067335

8

Association of human-leukocyte-antigen class I (B*0703) and class II (DRB1*0301) genotypes with susceptibility and resistance to the development of severe acute respiratory syndrome.

Ng MH, Lau KM, Li L, Cheng SH, Chan WY, Hui PK, Zee B, Leung CB, Sung JJ. Ng MH, et al. Among authors: cheng sh. J Infect Dis. 2004 Aug 1;190(3):515-8. doi: 10.1086/421523. Epub 2004 Jul 7. J Infect Dis. 2004. PMID: 15243926 Free PMC article.

9

Clonal evolution of 8p11 stem cell syndrome in a 14-year-old Chinese boy: a review of literature of t(8;13) associated myeloproliferative diseases.

Wong WS, Cheng KC, Lau KM, Chan NP, Shing MM, Cheng SH, Chik KW, Li CK, Ng MH. Wong WS, et al. Among authors: cheng kc, cheng sh. Leuk Res. 2007 Feb;31(2):235-8. doi: 10.1016/j.leukres.2006.04.015. Epub 2006 Jun 13. Leuk Res. 2007. PMID: 16777224

10

4q loss is potentially an important genetic event in MM tumorigenesis: identification of a tumor suppressor gene regulated by promoter methylation at 4q13.3, platelet factor 4.

Cheng SH, Ng MH, Lau KM, Liu HS, Chan JC, Hui AB, Lo KW, Jiang H, Hou J, Chu RW, Wong WS, Chan NP, Ng HK. Cheng SH, et al. Blood. 2007 Mar 1;109(5):2089-99. doi: 10.1182/blood-2006-04-018770. Epub 2006 Oct 31. Blood. 2007. PMID: 17077331 Free article.

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