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Marfan-like skeletal phenotype in the tight skin (Tsk) mouse.

Barisic-Dujmovic(Tatjana),Boban(Ivana),Adams… Calcif Tissue Int 2007-12-13

...Col1a1, BSP and OC was examined in marrow stromal cell cultures at various time points. A decrease in the rate of matura...

A clinical, histologic, and molecular study of 9 cases of congenital dermatofib…

Maire(Georges),Fraitag(Sylvie),Galmiche(Loui… Arch Dermatol 2007-03-16

...COL1A1-PDGFB) was detected by means of reverse transcriptase-polymerase chain reaction or fluorescence in situ hybridiza...

Expression and role of interleukin-6 in distraction osteogenesis.

Cho(T-J),Kim(J A),Chung(C Y),Yoo(W J),Gerste… Calcif Tissue Int 2007-08-20

...COL1A1 and osteopontin were not changed by IL-6 or its blocking antibody, but the alkaline phosphatase activities of MC3...

Epistatic interactions between genomic regions containing the COL1A1 gene and g…

Yang(Tie-Lin),Shen(Hui),Xiong(Dong-Hai),Xiao… Ann Hum Genet 2007-04-11

...COL1A1 (collagen type I alpha 1) gene and the genomic regions containing genes regulating osteoclast differentiation (e....

Target genes of myostatin loss-of-function in muscles of late bovine fetuses.

Cassar-Malek(Isabelle),Passelaigue(Florent),… BMC Genomics 2007-09-28

...COL1A1 and COL1A2, and up-regulation of COL4A2) and decreased adipocyte differentiation (down-regulation of C1QTNF3). Th...

Oxidative remodeling in pressure overload induced chronic heart failure.

Henderson(Brooke C),Tyagi(Neetu),Ovechkin(Al… Eur J Heart Fail 2007-09-20

...Col1a1 with 129 s background) mice. At 4 weeks, post surgery, functional parameters were measured. Left ventricle (LV) t...

Type III collagen is essential for growth acceleration of human osteoblastic ce…

Maehata(Yojiro),Takamizawa(Shinji),Ozawa(Shi… Matrix Biol 2007-09-19

...COL1A1 or COL1A2 messenger RNA levels. Transfection of MG-63 cells with siRNA for COL3A1 but not with that for COL1A1 de...

Expanding the phenotypic spectrum of Caffey disease.

Suphapeetiporn(K),Tongkobpetch(S),Mahayosnon… Clin Genet 2007-06-14

...COL1A1 was found in affected individuals, further confirming the autosomal dominance of Caffey disease that is caused by...

Osteogenesis imperfecta:epidemiology and pathophysiology.

Martin(Elizabeth),Shapiro(Jay R) Curr Osteoporos Rep 2007-12-18

...COL1A1 and COL1A2 mutations. Three new phenotypes have been added, of which one, type VII, is the result of mutations of...

Clinical and genetic analysis of two Tunisian otosclerosis families.

Ali(Insaf Bel Hadj),Thys(Melissa),Beltaief(N… Am J Med Genet A 2007-08-27

...COL1A1 and COL1A2, and NOG gene. In the family LK, linkage to all known loci was excluded. However, the family LS shows ...

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