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44篇 您的检索式：作者名="KERELY J"

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	题名	作者	年代	出处	被引量
1	X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein显示文摘	Kere J Srivastava AK Montonen O	1996	Nature Genet1996，13，4：	1
2	X - linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein 显示文摘	Kere J Srivastava AK Montonen O	1996	Nature Genet1996，13，：	1
3	X - linked anhidrotic ( hypohidrotic) ectodermal dysp lasia is caused by mutation in a novel transmembrane protein 显示文摘	Kere J Strivastavaa K Montonen O	1996	Nat Genet1996，13，4：	1
4	Positionally cloned susceptibility genes in allergy and asthma显示文摘	Kere J Laitinen T	2004	Curr Opin Immunol2004，16，：	1
5	Mapping and identifying genes for asthma and psoriasis 显示文摘	Kere J	2005	Philos Trans R Soc Lond B Biol Sci2005，360，1460：	1
6	X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein显示文摘	Kere J Srivastava AK Montonen O Zonana J Thomas N Ferguson B	1996	Nat Genet1996，13，4：	1
7	X-linked anhidrotic ectodermal dysplasia is caused by mutation in a novel transmembrane protein显示文摘	Kere J Srivastava AK Montonen O	1996	Nature Genetics1996，13，：	1
8	Positionally cloned susceptibility genes inallergy and asthma显示文摘	Kere J Laitinen T	2004	Curr Opin Immunol2004，16，6：	1
9	Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells显示文摘	Ezer S Bayes M Elomaa O Schlessinger D Kere J	1999	Hum Mol Genet1999，8，11：	1
10	Characterizing high- speed oscilloscopes 显示文摘	RUSH K DRAVING S KERELY J	1990	IEEE Spectrum September1990，27，：	1
11	Ectodysplasin,a protein required for epithelial morphogenesis,is a novel TNF homologue and promotes cell-matrix adhesion显示文摘	Mikkola ML Pispa J Pekkanen M Paulin L Nieminen P Kere J	1999	Mech Dev1999，88，2：	1
12	Characterizing high-speed oscilloscopes 显示文摘	RUSH K DRAVING S KERELY J	1990	IEEE Spectrum1990，1990，：	1
13	Familial amyloidosis, Finnish type: G654 mutation of the gelsolin gene in Finnish families and an unrelated American family显示文摘	de la Chapelle A Kere J Sack GH Jr Tolvanen R Maury CPJ	1992	Genomics1992，13，：	1
14	Determination of chlorantraniliprole residues in crops by liquid chromatography coupled with atmospheric pressure chemical ionization mass spectrometry/mass spectrometry 显示文摘	Grant J Rodgers C A Chic kering C D	2010	Journal of AOAC Intema- tional2010，，：	1
15	Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein显示文摘	Elomaa O Pulkkinen K Hannelius U Mikkola M Saarialho-Kere U Kere J	2001	Hum Mol Genet2001，10，9：	1
16	Genetic Disorders of MembraneTransport OL Congenital chloride diarrhea显示文摘	Kere J Lohi H Hoglund P	1999	Am J Physiol1999，276，11：	1
17	Positionally cloned susceptibility genes in allergy and asthma显示文摘	Kere J Laitinen T	2004	Curr Opin Immunol2004，16，：	1
18	SLC26A3 mutations incongenital chloride diarrhea 显示文摘	Makela S Kere J Holmberg C	2002	Hum Mutat2002，20，6：	1
19	early maternal smoking childhood wheezing显示文摘	Panasevich S Lindgren C Kere J	2010	Clin Exp Allergy2010，40，3：	1
20	X-linked anhidrotic(hypohidrotic)ectodermal dysplasia is cansed by mulation in a novel transmembrane protein显示文摘	Kere J Srivastava AK	1996	Nature Genet1996，13，4：	1

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