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18篇 您的检索式:作者名="Cleiren"
    题名 作者 年代 出处 被引量
1Binding-site identification and genotypic profiling of hepatitis C virus polymerasc inhibitors显示文摘Pauwels F Mostmans W Quirynen L M Mm van derHelm L Boutton C W Rueff A Cleiren E Rab 0,,:1
2The Binding Between Sclerostin and LRP5 is Altered by DKK1 and by High-Bone Mass LRP5 Mutations显示文摘Wendy Balemans Elke Piters Erna Cleiren Minrong Ai Liesbeth Wesenbeeck Matthew L. Warman Wim Hul 2008Calcified Tissue International2008,,6:1
3Six novel miasense mutations in the LDL receptorrelated protein 5 (LRP5) gene in different conditions with an increased bone density显示文摘Van Wesenbeeck L Cleiren E Gram J 0,,:1
4Psychological functioning of recently bereaved, middle-aged women : the fast 13 months 显示文摘Beem EE Maes S Cleiren M 2000Psychol Rep2000,87,1:1
5The binding between sclerostin and LRP5 is altered by Dkk-1 and by high-bone mass LRP5 mutation 显示文摘BALEMANS W PITERS E CLEIREN E 2008Calcif Tissue Int2008,82,6:1
6Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an Increased bone density显示文摘 Cleiren E Gram J 2003Am J Hum Genet2003,72,:1
7Albers-Schonberg disease (autosomal dominant osteopetrosis,type Ⅱ)results from mutations in the ClCN7 chloride channel gene显示文摘Cleiren E Beniehou O Van HE 2001Hum Molec Genet2001,10,25:1
8Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density显示文摘Van Wesenbeeck L Cleiren E Gram J 2003Am J Hum Genet2003,72,3:1
9Albers-Schonberg disease (autosomal dominant osteopetrosis,type Ⅱ) results from mutations in the ClCN7 chloride channel gene显示文摘CLEIREN E BENICHOU O VAN Hul E 2001Hum Mol Genet2001,10,:1
10Six novel missense mutations in the LDL recepter-related protein 5 (LRPS) gene in different conditions with increased bone density显示文摘Van wL Cleiren E Gram J 0,,03:1
11Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density显示文摘Van Wesenbeeck L Cleiren E Gram J 2003Am J Hum Genet2003,72,3:1
12The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)显示文摘Wim W Cleiren E Homfray T 2000J Med Genet2000,37,12:1
13The binding between Sclerostin and LRP5 is altered by DKKI and by highbone mass LRP5 mutations 显示文摘Balemans W Piters E Cleiren E 2008Calcif Tissue Int2008,82,6:1
14The binding between sclerostin and LRP5 is altered by DKKI and by high-bone mass LRP5 mutations 显示文摘Balemans W Piters E Cleiren E 2008Calcif Tissue Int2008,82,6:1
15Psychological functioning of re-cently bereaved,middle-aged women:the first 13 months显示文摘Beem EE Maes S Cleiren M 2000Psychol Rep2000,87,1:1
16Ibers- Schonberg dis- ease (autosomal dominant osteopetrosis,type 显示文摘Cleiren E Benichou O Van Hul E 2001Hum Mol Gen- et2001,10,:1
17Six novel mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density 显示文摘van Wesenbeeck L Cleiren E Gram J 2003Am J Hum Genet2003,72,:1
18Albers - Schonberg disease ( autosomal dominant osteopetrosis, type II) results from mutations in the CLCN7 chloride channel gene 显示文摘Cleiren E Benichou O van Hul E 2001Hum Mol Genet2001,10,25:1
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