Guan MX - Search Results

1

The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.

Liao Z, Zhao J, Zhu Y, Yang L, Yang A, Sun D, Zhao Z, Wang X, Tao Z, Tang X, Wang J, Guan M, Chen J, Li Z, Lu J, Guan MX. Liao Z, et al. Among authors: guan mx, guan m. Biochem Biophys Res Commun. 2007 Oct 26;362(3):670-6. doi: 10.1016/j.bbrc.2007.08.034. Epub 2007 Aug 15. Biochem Biophys Res Commun. 2007. PMID: 17723226 Free PMC article.

2

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.

Zhao L, Young WY, Li R, Wang Q, Qian Y, Guan MX. Zhao L, et al. Among authors: guan mx. Biochem Biophys Res Commun. 2004 Dec 24;325(4):1503-8. doi: 10.1016/j.bbrc.2004.10.199. Biochem Biophys Res Commun. 2004. PMID: 15555598

3

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

Wang Q, Li R, Zhao H, Peters JL, Liu Q, Yang L, Han D, Greinwald JH Jr, Young WY, Guan MX. Wang Q, et al. Among authors: guan mx. Am J Med Genet A. 2005 Feb 15;133A(1):27-30. doi: 10.1002/ajmg.a.30424. Am J Med Genet A. 2005. PMID: 15637703 Free PMC article.

4

Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.

Li R, Ishikawa K, Deng JH, Heman-Ackah S, Tamagawa Y, Yang L, Bai Y, Ichimura K, Guan MX. Li R, et al. Among authors: guan mx. Biochem Biophys Res Commun. 2005 Mar 4;328(1):32-7. doi: 10.1016/j.bbrc.2004.12.140. Biochem Biophys Res Commun. 2005. PMID: 15670746

5

Biochemical characterization of the deafness-associated mitochondrial tRNASer(UCN) A7445G mutation in osteosarcoma cell cybrids.

Li X, Zhang LS, Fischel-Ghodsian N, Guan MX. Li X, et al. Among authors: guan mx. Biochem Biophys Res Commun. 2005 Mar 11;328(2):491-8. doi: 10.1016/j.bbrc.2005.01.006. Biochem Biophys Res Commun. 2005. PMID: 15694374

6

Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation.

Qu J, Li R, Tong Y, Hu Y, Zhou X, Qian Y, Lu F, Guan MX. Qu J, et al. Among authors: guan mx. Biochem Biophys Res Commun. 2005 Mar 25;328(4):1139-45. doi: 10.1016/j.bbrc.2005.01.062. Biochem Biophys Res Commun. 2005. PMID: 15707996 Clinical Trial.

7

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH Jr, Guan MX. Young WY, et al. Among authors: guan mx. Biochem Biophys Res Commun. 2005 Mar 25;328(4):1244-51. doi: 10.1016/j.bbrc.2005.01.085. Biochem Biophys Res Commun. 2005. PMID: 15708009

8

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.

Li Z, Li R, Chen J, Liao Z, Zhu Y, Qian Y, Xiong S, Heman-Ackah S, Wu J, Choo DI, Guan MX. Li Z, et al. Among authors: guan mx. Hum Genet. 2005 Jun;117(1):9-15. doi: 10.1007/s00439-005-1276-1. Epub 2005 Apr 20. Hum Genet. 2005. PMID: 15841390 Free PMC article.

9

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.

Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX. Qian Y, et al. Among authors: guan mx. Biochem Biophys Res Commun. 2005 Jul 1;332(2):614-21. doi: 10.1016/j.bbrc.2005.05.003. Biochem Biophys Res Commun. 2005. PMID: 15896721

10

Rational design of an EGF-IL18 fusion protein: implication for developing tumor therapeutics.

Lu JX, Peng Y, Meng ZF, Jin LQ, Lu YS, Guan MX. Lu JX, et al. Among authors: guan mx. Biochem Biophys Res Commun. 2005 Aug 19;334(1):157-61. doi: 10.1016/j.bbrc.2005.06.076. Biochem Biophys Res Commun. 2005. PMID: 15993840

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