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1000 Results:AA:M H CHO 0.578 sec.
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361
Sustained phosphorylation of mutated FGFR3 is a crucial feature of genetic dwarfism and induces apoptosis in the ATDC5 chondrogenic cell line via PLCγ-activated STAT1
Sustained phosphorylation of mutated FGFR3 is a crucial feature of genetic dwarfism and induces apoptosis in the ATDC5 chondrogenic cell line via PLCγ-activated STAT1
Harada, D., | Elsevier Inc | 2007 ,
362
Association between an intronic apolipoprotein E polymorphism and bone mineral density in Singaporean Chinese females
Association between an intronic apolipoprotein E polymorphism and bone mineral density in Singaporean Chinese females
Tong, T. Y., | Elsevier Inc | 2010 ,
363
Hand2 regulates chondrogenesis in vitro and in vivo
Hand2 regulates chondrogenesis in vitro and in vivo
Abe, M., | Elsevier Inc | 2010 ,
364
Heparanase expression and activity influences chondrogenic and osteogenic processes during endochondral bone formation
Heparanase expression and activity influences chondrogenic and osteogenic processes during endochondral bone formation
Brown, A. J., | Elsevier Inc | 2008 ,
365
Bax deficiency in mice increases cartilage production during fracture repair through a mechanism involving increased chondrocyte proliferation without changes in apoptosis
Bax deficiency in mice increases cartilage production during fracture repair through a mechanism involving increased chondrocyte proliferation without changes in apoptosis
Rundle, C. H., | Elsevier Inc | 2008 ,
366
Roles of the endoplasmic reticulum stress transducer OASIS in fracture healing
Roles of the endoplasmic reticulum stress transducer OASIS in fracture healing
Funamoto, T, | Elsevier Inc | 2011 ,
367
Altered fracture callus formation in chondromodulin-I deficient mice
Altered fracture callus formation in chondromodulin-I deficient mice
Yukata, K., | Elsevier Inc | 2008 ,
368
Cortical bone health shows significant linkage to chromosomes 2p, 3p, and 17q in 10-year-old children
Cortical bone health shows significant linkage to chromosomes 2p, 3p, and 17q in 10-year-old children
Duren, D. L, | Elsevier Inc | 2011 ,
369
Association between serum cholesterol and bone mineral density
Association between serum cholesterol and bone mineral density
Makovey, J., | Elsevier Inc | 2009 ,
370
The primary site of the acrocephalic feature in Apert syndrome is a dwarf cranial base with accelerated chondrocytic differentiation due to aberrant activation of the FGFR2 signaling
The primary site of the acrocephalic feature in Apert syndrome is a dwarf cranial base with accelerated chondrocytic differentiation due to aberrant activation of the FGFR2 signaling
Nagata, M., | Elsevier Inc | 2011 ,
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