He L - Search Results

1

SASH1 regulates melanocyte transepithelial migration through a novel Gαs-SASH1-IQGAP1-E-Cadherin dependent pathway.

Zhou D, Wei Z, Deng S, Wang T, Zai M, Wang H, Guo L, Zhang J, Zhong H, He L, Xing Q. Zhou D, et al. Among authors: he l. Cell Signal. 2013 Jun;25(6):1526-38. doi: 10.1016/j.cellsig.2012.12.025. Epub 2013 Jan 16. Cell Signal. 2013. PMID: 23333244

2

A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.

Xing QH, Wang MT, Chen XD, Feng GY, Ji HY, Yang JD, Gao JJ, Qin W, Qian XQ, Wu SN, He L. Xing QH, et al. Among authors: he l. Am J Hum Genet. 2003 Aug;73(2):377-82. doi: 10.1086/377007. Epub 2003 Jun 12. Am J Hum Genet. 2003. PMID: 12815562 Free PMC article.

3

Association analysis of polymorphisms in the upstream region of the human dopamine D4 receptor gene in schizophrenia.

Xing QH, Wu SN, Lin ZG, Li HF, Yang JD, Feng GY, Wang MT, Yang WW, He L. Xing QH, et al. Among authors: he l. Schizophr Res. 2003 Dec 1;65(1):9-14. doi: 10.1016/s0920-9964(03)00064-1. Schizophr Res. 2003. PMID: 14623368

4

[Genetic analysis of a Chinese pedigree with congenital synpolydactyly].

Qin W, Shu AL, Xing QH, Yang MS, Feng GY, He L. Qin W, et al. Among authors: he l. Yi Chuan Xue Bao. 2003 Oct;30(10):973-7. Yi Chuan Xue Bao. 2003. PMID: 14669516 Chinese.

5

A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis-ptosis-epicanthus inversus.

Qian X, Shu A, Qin W, Xing Q, Gao J, Yang J, Feng G, He L. Qian X, et al. Among authors: he l. Mutat Res. 2004 Oct 4;554(1-2):19-22. doi: 10.1016/j.mrfmmm.2004.02.014. Mutat Res. 2004. PMID: 15450400

6

Response to chlorpromazine treatment may be associated with polymorphisms of the DRD2 gene in Chinese schizophrenic patients.

Wu S, Xing Q, Gao R, Li X, Gu N, Feng G, He L. Wu S, et al. Among authors: he l. Neurosci Lett. 2005 Mar 7;376(1):1-4. doi: 10.1016/j.neulet.2004.11.014. Epub 2004 Dec 2. Neurosci Lett. 2005. PMID: 15694263

7

A family-based association study of schizophrenia with polymorphisms at three candidate genes.

Duan S, Gao R, Xing Q, Du J, Liu Z, Chen Q, Wang H, Feng G, He L. Duan S, et al. Among authors: he l. Neurosci Lett. 2005 Apr 29;379(1):32-6. doi: 10.1016/j.neulet.2004.12.040. Epub 2005 Jan 12. Neurosci Lett. 2005. PMID: 15814194

8

Identification of a novel ADAR mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH).

Xing Q, Wang M, Chen X, Qian X, Qin W, Gao J, Wu S, Gao R, Feng G, He L. Xing Q, et al. Among authors: he l. Arch Dermatol Res. 2005 Sep;297(3):139-42. doi: 10.1007/s00403-005-0589-1. Epub 2005 Sep 29. Arch Dermatol Res. 2005. PMID: 16133458

9

Association of DRD2 polymorphisms and chlorpromazine-induced extrapyramidal syndrome in Chinese schizophrenic patients.

Wu SN, Gao R, Xing QH, Li HF, Shen YF, Gu NF, Feng GY, He L. Wu SN, et al. Among authors: he l. Acta Pharmacol Sin. 2006 Aug;27(8):966-70. doi: 10.1111/j.1745-7254.2006.00355.x. Acta Pharmacol Sin. 2006. PMID: 16867246

10

No observable relationship between the ACE gene insertion/deletion polymorphism and psychometric IQ and psychomotor ability in Chinese children.

Gao J, Gao X, Qin W, Dang F, Zhang F, Qian X, Zeng X, Xing Q, Zheng Z, Li J, Guo T, Chang H, Feng G, He L. Gao J, et al. Among authors: he l. Neuropsychobiology. 2006;53(4):196-202. doi: 10.1159/000094728. Epub 2006 Jul 26. Neuropsychobiology. 2006. PMID: 16874006

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