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Increased Expression of Several Collagen Genes is Associated with Drug Resist...

Januchowski(Radosław),Świerczewska(Monika)... J Cancer 2016-07-08

...COL1A2, COL15A1 and COL21A1. 3. Gene with a very high level of expression: COL3A1. Expression of collagen (COL) proteins...

Targeting the annulus fibrosus of the intervertebral disc: Col1a2-Cre(ER)T mi...

Bedore(Jake),Quesnel(Katherine),Quinonez(D... J Cell Commun Signal 2016-05-27

...Col1a2-Cre(ER)T;ROSA26mTmG mice possessing a tamoxifen-dependent Cre recombinase driven by a Cola2 promoter and distal e...

Osteogenesis imperfecta caused by PPIB mutation with severe phenotype and con...

Rush(Eric T),Caldwell(Kathleen S),Kreikeme... J Pediatr Genet 2016-09-14

...COL1A2. A number of other genes causative of this disorder have been found, including PPIB, which forms one subunit of t...

Molecular cloning of type I collagen cDNA and nutritional regulation of type ...

Yu(E M),Liu(B H),Wang(G J),Yu(D G),Xie(J),... J Anim Physiol Anim Nutr (B... 2015-03-30

...COL1A2) on the basis of our isolation of COL1A1. The COL1A2 cDNA was found to be 4899 bp in length and included a 4059-b...

Two Japanese familial cases of Caffey disease with and without the common COL...

Kitaoka(Taichi),Miyoshi(Yoko),Namba(Noriyu... Eur J Pediatr 2015-02-04

...COL1A2 genes and measured bone mineral density in two Japanese familial cases of Caffey disease. The index case and two ...

Targeting the LRP5 pathway improves bone properties in a mouse model of osteo...

Jacobsen(Christina M),Barber(Lauren A),Ayt... J Bone Miner Res 2015-06-09

...Col1a2(+/p.G610C) mice, which model human type IV OI. We found that Col1a2(+/p.G610C) ;Lrp5(+/p.A214V) offspring had sig...

Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogen...

Stephen(Joshi),Shukla(Anju),Dalal(Ashwin),... Am J Med Genet A 2015-01-13

...COL1A2 genes. Since these two genes are very large, there are no data about mutations in Indian patients with OI. We sel...

Induced ablation of Bmp1 and Tll1 produces osteogenesis imperfecta in mice.

Muir(Alison M),Ren(Yinshi),Butz(Delana Hop... Hum Mol Genet 2015-01-12

...COL1A2, whereas rarer recessive OI is often caused by mutations in genes encoding collagen I-interacting proteins. Recen...

p38 MAP kinase inhibitor suppresses transforming growth factor-β2-induced typ...

Inoue-Mochita(Miyuki),Inoue(Toshihiro),Fuj... PLoS One 2015-12-15

...COL1A2. These effects were significantly inhibited by SB203580, but not Y-27632. Additionally, Y-27632 did not significa...

Genetic screening of a pedigree with osteogenesis imperfecta type Ⅰ and ident...

Rong(Li),Yuanping(Guo),Jingxin(Pan),Yibin(... Yi Chuan 2015-03-24

...COL1A2 (Collagen, type Ⅰ, alpha 2) genes in a child with OI type Ⅰ were screened using PCR-DNA direct sequencing. The re...

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