Bai RK - Search Results

1

Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: a single-step approach.

Bai RK, Wong LJ. Bai RK, et al. Clin Chem. 2004 Jun;50(6):996-1001. doi: 10.1373/clinchem.2004.031153. Epub 2004 Apr 8. Clin Chem. 2004. PMID: 15073091

2

Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer.

Tan DJ, Bai RK, Wong LJ. Tan DJ, et al. Among authors: bai rk. Cancer Res. 2002 Feb 15;62(4):972-6. Cancer Res. 2002. PMID: 11861366

3

A cystic fibrosis patient with two novel mutations in mitochondrial DNA: mild disease led to delayed diagnosis of both disorders.

Wong LJ, Liang MH, Kwon H, Bai RK, Alper O, Gropman A. Wong LJ, et al. Among authors: bai rk. Am J Med Genet. 2002 Nov 15;113(1):59-64. doi: 10.1002/ajmg.10767. Am J Med Genet. 2002. PMID: 12400067

4

Comprehensive scanning of the entire mitochondrial genome for mutations.

Wong LJ, Liang MH, Kwon H, Park J, Bai RK, Tan DJ. Wong LJ, et al. Among authors: bai rk. Clin Chem. 2002 Nov;48(11):1901-12. Clin Chem. 2002. PMID: 12406974

5

Enhanced detection of deleterious mutations by TTGE analysis of mother and child's DNA side by side.

Kwon H, Tan DJ, Bai RK, Wong LJ. Kwon H, et al. Among authors: bai rk. Ann N Y Acad Sci. 2004 Apr;1011:299-303. doi: 10.1007/978-3-662-41088-2_28. Ann N Y Acad Sci. 2004. PMID: 15126305

6

Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease.

Bai RK, Perng CL, Hsu CH, Wong LJ. Bai RK, et al. Ann N Y Acad Sci. 2004 Apr;1011:304-9. doi: 10.1007/978-3-662-41088-2_29. Ann N Y Acad Sci. 2004. PMID: 15126306

7

Hearing loss in mitochondrial disorders.

Hsu CH, Kwon H, Perng CL, Bai RK, Dai P, Wong LJ. Hsu CH, et al. Among authors: bai rk. Ann N Y Acad Sci. 2005 May;1042:36-47. doi: 10.1196/annals.1338.004. Ann N Y Acad Sci. 2005. PMID: 15965043

8

Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease.

Bai RK, Wong LJ. Bai RK, et al. J Mol Diagn. 2005 Nov;7(5):613-22. doi: 10.1016/S1525-1578(10)60595-8. J Mol Diagn. 2005. PMID: 16258160 Free PMC article.

9

Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load.

Enns GM, Bai RK, Beck AE, Wong LJ. Enns GM, et al. Among authors: bai rk. Mol Genet Metab. 2006 Aug;88(4):364-71. doi: 10.1016/j.ymgme.2006.02.001. Epub 2006 Mar 20. Mol Genet Metab. 2006. PMID: 16546428

10

Significance of somatic mutations and content alteration of mitochondrial DNA in esophageal cancer.

Tan DJ, Chang J, Liu LL, Bai RK, Wang YF, Yeh KT, Wong LJ. Tan DJ, et al. Among authors: bai rk. BMC Cancer. 2006 Apr 18;6:93. doi: 10.1186/1471-2407-6-93. BMC Cancer. 2006. PMID: 16620376 Free PMC article.

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