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20篇 您的检索式：作者名="Doding J"

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	题名	作者	年代	出处	被引量
1	The complex genetics of Kallmann syndrome KALl, FCFRI , FCF8, PROKR2, PROK2 显示文摘	HARDELIN J P DODE C	2008	Sex Dev2008，2，45：	1
2	Loss of function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘	DODE C LEVILLIERS J DUPONT J M	2001	Proc Natl Acad Sci2001，98，13：	1
3	Loss of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘	DODE C LEVILLIERS J DUPON J	2003	NatGenet2003，33，4：	1
4	Diseases in- volving the Golgi calcium pump 显示文摘	Vanoevelen J Dode L Raeymaekers L	2007	Subeell Biochem2007，45，：	1
5	Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘	Dode C Levilliers J Dupont JM	2003	Nat Genet2003，33，4：	1
6	Kallmann syndrome : mutations in the genes encoding prokineticin-2 and prokineticin receptor-2 显示文摘	Dode C Teixeira L Levilliers J	2006	Plos Genet2006，2，10：	1
7	Effect of Hailey-Hailey Disease mutations on the function of a new variant of human secretory pathway Ca2+/Mn2+-ATPase (hSPCA1)显示文摘	Fairclough RJ Dode L Vanoevelen J	2003	J Biol Chem2003，278，24：	1
8	Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘	Dode C Levilliers J Dupont J M	2003	Nat Genet2003，33，4：	1
9	Kallmann syndrome:mutations in the genes encoding prokineticin-2 and prokineticin receptor-2显示文摘	Dode C Teixeira L Levilliers J	2006	PLo S Genet2006，2，10：	1
10	Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘	Levilliers J Dupont JM	2003	Nat Genet2003，33，4：	1
11	Kallmann syndrome:fibroblast growth factor signaling insufficiency?显示文摘	Dode C Hardelin J P	2004	J Mol Med(Berl)2004，82，11：	1
12	Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokinetiein receptor-2显示文摘	Dode C Teixeira L Levilliers J	2006	PLoS Genet2006，2，10：	1
13	Early or delayed enteral feeding for preterm growth-restricted infants: a randomized tri- M 显示文摘	Leaf A Doding J Kempley S	2012	Pediatrics2012，129，5：	1
14	The nature of pep- tides presented by an HLA class I low expression allele显示文摘	Hinrichs J Foil D Bade Doding C	2010	Haematologica2010，95，8：	1
15	Early or delayed enteral feeding for preterm growth-restricted infants: a randomized trial 显示文摘	Leaf A Doding J Kempley S	2012	Pediatrics2012，129，5：	1
16	The secretory pathway Ca2+/Mn2+-ATPase 2 is a Golgi-localized pump with high affinity for Ca2+ ions显示文摘	Vanoevelen J Dode L Van Baelen K		0，，24：	1
17	Early or delayed enteral feeding for preterm growth-restricted infants:a randomized trial显示文摘	Leaf A Doding J Kempley S		0，，5：	1
18	Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘	DODE C LEVILLIERS J DUPONT J M	2003	Nat Genet2003，33，：	1
19	Cytosolic Ca2+ signals depending on the functional state of the Golgi in HeLa cells显示文摘	Vanoevelen J Raeymaekers L Dode L		0，，：	1
20	Kalhnann syndrome eaused by mutations in the PROK2 and PROKR2 genes: pathophysiolo-gy and genotype-phenotype correlations显示文摘	Sarfati J Dode C Young J	2010	Front Horm Res2010，39，：	1

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