主页文献库搜索
Gene expression profiles reflect sclerosing cholangitis activity in abcb4 (-/...

Nakken(Karl E),Nygard(Stale),Haaland(Teres... Scand J Gastroenterol 2009-06-23

...Col1a2 and Col4a1 genes paralleled the unequal SC activities of CA- and UDCA-fed abcb4 (-/-) mice.,The numbers of differ...

Comparative phenotypic analysis of articular chondrocytes cultured within typ...

Freyria(Anne-Marie),Ronzière(Marie-Claire)... Tissue Eng Part A 2009-09-10

...COL1A2 mRNA and alpha10/alpha11 integrin subunit mRNA, was comparatively better sustained in type I collagen sponges whe...

Combination of microarray profiling and protein-protein interaction databases...

Wong(Fen-Hwa),Huang(Chi-Ying F),Su(Li-Jen)... Int J Oncol 2009-02-24

...COL1A2, MMP9, CD44, FN1, TGFBI, PXN, SPARC and VWF) were associated with tumor metastasis and formed a highly interactiv...

Polymorphism rs42524 of COL1A2 and sporadic intracranial aneurysms in the Chi...

Zhu(Yufang),Li(Weiju),Ge(Mingxu),Xu(Shangc... J Neurosurg 2009-01-07

...COL1A2 and the occurrence of sporadic IAs in Chinese patients.,The polymorphism rs42524 of the COL1A2 gene was identifie...

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia...

Barron(Martin J),McDonnell(Sinead T),Macki... Orphanet J Rare Dis 2009-01-27

...COL1A2, underlie this condition. All other forms of DGI and DD, except DD-1, appear to result from mutations in the gene...

Connective tissue and related disorders and preterm birth: clues to genes con...

Anum(E A),Hill(L D),Pandya(A),Strauss(J F) Placenta 2009-05-14

...COL1A2, TNXB, PLOD1, ADAMTS2, CRTAP, LEPRE1 and ZMPSTE24. Marfan syndrome, caused by FBN1 mutations, and polymorphisms i...

Chondroitin sulphate decreases collagen synthesis in normal and scleroderma f...

Renard(Emmanuelle),Chadjichristos(Christos... J Cell Mol Med 2009-03-25

...COL1A2) in either physiological or pathological situations, such as scleroderma, are not completely known. In this study...

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.

Baldridge(Dustin),Schwarze(Ulrike),Morello... Hum Mutat 2009-01-08

Autosomal dominant osteogenesis imperfecta (OI) is caused by mutations in the genes (COL1A1 or COL1A2) encoding the chai...

Expression of collagen types I, II and III in juvenile angiofibromas.

Gramann(M),Wendler(O),Haeberle(L),Schick(B... Cells Tissues Organs 2009-06-25

...Col1A2 (p < 0.001) and Col3A1 (p < 0.001) mRNA levels in JAs, compared with NM. Western blot analysis and immunohistoche...

CpG hypermethylation of collagen type I alpha 2 contributes to proliferation ...

Mori(Katsuhisa),Enokida(Hideki),Kagara(Ich... Int J Oncol 2009-08-18

...COL1A2) gene was the most up-regulated among the 30,144 genes screened. We hypothesize that inactivation of the COL1A2 g...

上一页 54 55 56 57 58 59 60 61 62 下一页 58 / 共 110

联系地址

山东省济南市章丘区文博路2号

齐鲁师范学院 genelibs生信实验室

山东省济南市高新区舜华路750号

大学科技园北区F座4单元2楼

电话: 0531-88819269

微信公众号

关注微信订阅号,实时查看信息,关注医学生物学动态。


商务邮箱

E-mail: [email protected]