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No association between polymorphisms and haplotypes of COL1A1 and COL1A2 gene...

Hu(Wei-wei),He(Jin-wei),Zhang(Hao),Wang(Ch... Acta Pharmacol Sin 2011-10-24

...COL1A2 genes affected the onset of fracture in postmenopausal Chinese women.,SNPs in COL1A1 and COL1A2 genes were identi...

Elevated CCN2 expression in scleroderma: a putative role for the TGFβ accesso...

Holmes(Alan M),Ponticos(Markella),Shi-Wen(... J Cell Commun Signal 2011-11-10

...COL1A2) and CCN2. Previously we have shown elevated expression of the TGFβ accessory receptor, endoglin on Systemic Scle...

Smad interacting protein 1 as a regulator of skin fibrosis in pathological sc...

Zhang(Zhan-Feng),Zhang(Yan-Gang),Hu(Da-Hai... Burns 2011-07-22

...COL1A2) and directly correlates with the mRNA level of matrix metalloproteinase-1 (MMP1). Overexpression of SIP1 in kelo...

The protective effects of long-term oral administration of marine collagen hy...

Liang(Jiang),Pei(Xinrong),Zhang(Zhaofeng),... J Food Sci 2011-08-23

...COL1A2 and COL3A1) through activating Smad signaling pathway with up-regulated TGF-βRII (TβRII) expression level. Meanwh...

Osteopontin modulates inflammation, mucin production, and gene expression sig...

Sabo-Attwood(Tara),Ramos-Nino(Maria E),Eug... Am J Pathol 2011-08-26

...Col1a2, Timp1, Tnc, Eln, and Col3a1) linked to fibrosis via initiation and cross talk between IL-1β and epidermal growth...

A microRNA circuit mediates transforming growth factor-β1 autoregulation in r...

Kato(Mitsuo),Arce(Laura),Wang(Mei),Putta(S... Kidney Int 2011-12-07

...Col1a2, Col4a1, and TGF-β1 in mouse mesangial cells, and in mouse kidney cortex. Thus, miRNA-regulated circuits may ampl...

Genetics of bone diseases: Paget's disease, fibrous dysplasia, osteopetrosis,...

Michou(Laetitia),Brown(Jacques P) Joint Bone Spine 2011-08-30

...COL1A2 genes are found in over 90% of patients. The recent identification of mutations in the CRTAP, LEPRE1, and PPIB ge...

Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrom...

Kelley(Brian P),Malfait(Fransiska),Bonafe(... J Bone Miner Res 2011-05-25

...COL1A2) encoding the chains of type I collagen. Bruck syndrome is a recessive disorder featuring congenital contractures...

Collagen gene polymorphisms influence fracture risk and bone mass acquisition...

Blades(H Z),Arundel(P),Carlino(W A),Dalton... Bone 2011-01-24

...COL1A2, bone mass acquisition, and childhood fractures are unclear. We recruited 394 children and adolescents aged 4 to ...

Cranial base abnormalities in osteogenesis imperfecta: phenotypic and genotyp...

Cheung(Moira S),Arponen(Heidi),Roughley(Pe... J Bone Miner Res 2011-04-28

...COL1A2 mutations, and in 17% of patients with splice-site mutations affecting either COL1A1 or COL1A2. However, multivar...

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