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27篇 您的检索式：作者名="Sobacchi"

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	题名	作者	年代	出处	被引量
1	The genetic and biochemical basis of Omenn syndrome显示文摘	Santagata S Villa A Sobacchi C	2000	Immunol Rev2000，178，：	1
2	Human osteoc-Jast- poor osteopetrosis with hypogammaglobulinemia due to TNFRSFIIA(RANK)mutations显示文摘	Guerrini MM Sobacchi C Cassani B	2008	Am J Hum Cenet2008，83，：	1
3	Prenatal diagnosis of RAG-deficient Omenn syndrome显示文摘	Villa A Bozzi F Sobacchi C	2000	Prenat Diagn2000，20，1：	1
4	Experimental assessment of pulsed corona discharge for treatment of VOC emissions显示文摘	Sobacchi M G Saveliev A V Fridman A A	2003	Plasma Chem Plasma Process2003，23，2：	1
5	Infantile Malignant, Autosomal Recessive Osteopetrosis: The Rich and The Poor显示文摘	Anna Villa Matteo M. Guerrini Barbara Cassani Alessandra Pangrazio Cristina Sobacchi	2009	Calcified Tissue International2009，，1：	1
6	Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations显示文摘	Guerrini MM Sobacchi C Cassani B Abinun M Kilic SS Pangrazio A Moratto D Mazzolari E Clayton-Smith J Orchard P Coxon FP Helfrich MH Crockett JC Mellis D Vellodi A Tezcan I N otarangelo L D R ogers MJ V ezzoni P V illa A F rattini A		0，，：	1
7	显示文摘	Villa A Sobacchi C Vezzoi P	2001	Curr Opin Allergy Clin Immunol2001，1，6：	1
8	显示文摘	Villa A Sobacchi c Nortarangelo LD	2001	Blood2001，97，1：	1
9	Osteoclast- poor human osteopetrosis due to mutations in the gene enco- ding RANKL显示文摘	Sobacchi C Frattini A Guerrini MM	2007	Nat Genet2007，39，：	1
10	Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSFI1A(RANK)mutations显示文摘	Guerrini MM Sobacchi C Cassarli B	2008	Am J Hum Genet2008，83，1：	1
11	Osteoclast-poor osteopetrosis due to mutations in the gene encoding RANKL 显示文摘	Sobacchi C Frattini A Guerrini MM	2007	Nat Geuet2007，39，3：	1
12	Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis显示文摘	Frattini A Orchard PJ Sobacchi C	2000	Nature Genet2000，25，：	1
13	The mutational spectrum of human malignant autosomal recessive osteopetrosis 显示文摘	Sobacchi C Frattini A Orchard P	2001	HumMolGenet2001，10，17：	1
14	Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of humanautosomal recessive osteopetrosis显示文摘	Frattini A Orchard PJ Sobacchi C	2000	Nat Genet2000，25，：	1
15	The mutational spectrum of human malignant autosomal recessive osteopetrosis 显示文摘	Sobacchi C Frattini A Orchard P	2001	Hum Mol Genet2001，10，17：	1
16	Defects in TCIRG1 subunit of the vacuo- lar proton pump are responsible for a sub- set of human autosomal recessive osteopet- rosis显示文摘	Frattini A Orchard PJ Sobacchi C	2000	Nat Genet2000，25，3：	1
17	Humarl osteo- clast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSFllA(RANK) mutations 显示文摘	Guerrini M M Sobacchi C Cassani B	2008	Am J Hum Genet2008，83，1：	1
18	Osteopetrosis : genetics, treatment and new insights into osteoclast func- tion显示文摘	Sobacchi C Schulz A Coxon FP	2013	Nat Rev Endocrinol2013，9，9：	1
19	Experimental assessment of pulsed corona discharge for treatment of VOC emissions 显示文摘	SOBACCHI M G SAYELIEV A V FRIDMAN A A	2003	Plasma Chemical and Plasma Process2003，23，2：	1
20	Osteopetrosis:genetics, treatment and new insights into osteoclast function显示文摘	Sobacchi C Schulz A Coxon FP	2013	Nat Rev Endocrinol2013，9，：	1

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