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1.
Role of the TSLP-DC-OX40L pathway in asthma pathogenesis and airway inflammation in mice.
Biochem Cell Biol
; 96(3): 306-316, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29024606
2.
[Role of transient receptor potential vanilloid 1 in airway inflammation in asthmatic mice].
Zhongguo Dang Dai Er Ke Za Zhi
; 18(9): 874-878, 2016 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-27655547
3.
[Investigation and OCRL mutation analysis of a family with oculocerebrorenal syndrome of Lowe].
Zhongguo Dang Dai Er Ke Za Zhi
; 16(4): 366-9, 2014 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-24750831
4.
[Site-directed mutagenesis and protein expression of SCN5A gene associated with congenital long QT syndrome].
Zhongguo Dang Dai Er Ke Za Zhi
; 15(3): 223-6, 2013 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-23498767
5.
[Clinical manifestations and gene mutations of a Chinese family with MYH9-related syndrome].
Zhongguo Dang Dai Er Ke Za Zhi
; 14(9): 678-82, 2012 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-22989438
6.
[Site-directed mutagenesis and protein expression of KCNQ2 gene associated with neonatal convulsions].
Zhongguo Dang Dai Er Ke Za Zhi
; 13(8): 611-6, 2011 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-21849107
7.
[WASP gene mutation analysis of a family of X-linked thrombocytopenia].
Zhongguo Dang Dai Er Ke Za Zhi
; 12(10): 784-7, 2010 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-20959042
8.
[Linkage analysis and gene mapping of one Chinese family with benign familial infantile convulsions].
Zhongguo Dang Dai Er Ke Za Zhi
; 12(2): 89-92, 2010 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-20199718
9.
Phenytoin-responsive epileptic encephalopathy with a tandem duplication involving FGF12.
Neurol Genet
; 3(1): e133, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-28144627
10.
Site-directed mutagenesis of neonatal convulsions associated KCNQ2 gene and its protein expression.
Transl Pediatr
; 1(2): 91-8, 2012 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26835270
11.
[Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three].
Zhonghua Er Ke Za Zhi
; 47(12): 926-30, 2009 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-20193146
12.
[A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family].
Zhonghua Er Ke Za Zhi
; 44(7): 487-91, 2006 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-17044971
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