Hsieh LJ - Search Results

1

Functional genomic analysis identified epidermal growth factor receptor activation as the most common genetic event in oral squamous cell carcinoma.

Sheu JJ, Hua CH, Wan L, Lin YJ, Lai MT, Tseng HC, Jinawath N, Tsai MH, Chang NW, Lin CF, Lin CC, Hsieh LJ, Wang TL, Shih IeM, Tsai FJ. Sheu JJ, et al. Among authors: hsieh lj. Cancer Res. 2009 Mar 15;69(6):2568-76. doi: 10.1158/0008-5472.CAN-08-3199. Epub 2009 Mar 10. Cancer Res. 2009. PMID: 19276369

2

Genomic alterations in human malignant glioma cells associate with the cell resistance to the combination treatment with tumor necrosis factor-related apoptosis-inducing ligand and chemotherapy.

Li YC, Tzeng CC, Song JH, Tsia FJ, Hsieh LJ, Liao SJ, Tsai CH, Van Meir EG, Hao C, Lin CC. Li YC, et al. Among authors: hsieh lj. Clin Cancer Res. 2006 May 1;12(9):2716-29. doi: 10.1158/1078-0432.CCR-05-1980. Clin Cancer Res. 2006. PMID: 16675563

3

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.

Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ. Lin CC, et al. Among authors: hsieh yy, hsieh lj. Prenat Diagn. 2006 Oct;26(10):898-902. doi: 10.1002/pd.1520. Prenat Diagn. 2006. PMID: 16915592

4

Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.

Chen CP, Wang TH, Lin CC, Tsai FJ, Hsieh LJ, Wang W. Chen CP, et al. Among authors: hsieh lj. J Formos Med Assoc. 2008 Oct;107(10):822-6. doi: 10.1016/S0929-6646(08)60197-7. J Formos Med Assoc. 2008. PMID: 18926951 Free article.

5

Complex genomic organization of Indian muntjac centromeric DNA.

Cheng YM, Li TS, Hsieh LJ, Hsu PC, Li YC, Lin CC. Cheng YM, et al. Among authors: hsieh lj. Chromosome Res. 2009;17(8):1051-62. doi: 10.1007/s10577-009-9097-z. Epub 2009 Nov 18. Chromosome Res. 2009. PMID: 19921447

6

Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.

Chen CP, Lin CC, Li YC, Hsieh LJ, Lee CC, Wang W. Chen CP, et al. Among authors: hsieh lj. Fertil Steril. 2006 Nov;86(5):1514.e1-2. doi: 10.1016/j.fertnstert.2006.02.127. Fertil Steril. 2006. PMID: 17070202 Free article.

7

Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).

Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2006 Apr;26(4):313-20. doi: 10.1002/pd.1399. Prenat Diagn. 2006. PMID: 16506269 Review.

8

Sumoylation of p45/NF-E2: nuclear positioning and transcriptional activation of the mammalian beta-like globin gene locus.

Shyu YC, Lee TL, Ting CY, Wen SC, Hsieh LJ, Li YC, Hwang JL, Lin CC, Shen CK. Shyu YC, et al. Among authors: hsieh lj. Mol Cell Biol. 2005 Dec;25(23):10365-78. doi: 10.1128/MCB.25.23.10365-10378.2005. Mol Cell Biol. 2005. PMID: 16287851 Free PMC article.

9

Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.

Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2006 Feb;26(2):138-46. doi: 10.1002/pd.1369. Prenat Diagn. 2006. PMID: 16470734 Review.

10

Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).

Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2005 Feb;25(2):112-8. doi: 10.1002/pd.1083. Prenat Diagn. 2005. PMID: 15712324 Review.

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