Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Omar Hauache"'
Autor:
Ana Claudia Ramalho, Marise Lazaretti-Castro, Omar Hauache, José Gilberto Vieira, Edmilson Takata, Francisco Cafalli, Fernando Tavares
Publikováno v:
São Paulo Medical Journal, Vol 119, Iss 2, Pp 48-53
CONTEXT: It is believed that about 25% of menopausal women in the USA will exhibit some kind of fracture as a consequence of osteoporosis. Fractures of the proximal femur are associated with a greater number of deaths and disabilities and higher medi
Externí odkaz:
https://doaj.org/article/3b63046aac5148988e0a320f5be588cb
Publikováno v:
Endocrinology. 141:4156-4163
Naturally occurring mutations identified in subjects with autosomal dominant hypocalcemia (ADH) and the calcimimetic compound, R-568, have both been reported to increase Ca2+ sensitivity of the Ca2+ receptor (CaR). To gain insight into their mechanis
Publikováno v:
Journal of Biological Chemistry. 275:16382-16389
The 612-residue extracellular domain of the human Ca(2+) receptor (hCaR) has been speculated to consist of a Venus's-flytrap domain (VFT) and a cysteine-rich domain. We studied the function of the hCaR Cys-rich domain by using mutagenesis and chimera
Publikováno v:
Endocrine. 13:63-70
We studied the activity of mutants involving the aminoterminal extracellular, seven-transmembrane (7TM) and carboxy-terminal tail domains of the human Ca2+ receptor to gain insight into the functional interactions between these domains during recepto
Autor:
Allen M. Spiegel, Paul K. Goldsmith, Benjamin C. Hauschild, Peter J. Steinbach, Omar Hauache, Kausik Ray
Publikováno v:
Journal of Biological Chemistry. 274:27642-27650
We analyzed the effect of substituting serine for each of the 19 cysteine residues within the amino-terminal extracellular domain of the human Ca(2+) receptor on cell surface expression and receptor dimerization. C129S, C131S, C437S, C449S, and C482S
Publikováno v:
FEBS letters. 448(1)
A missense mutation, A843E, in the seventh transmembrane domain of the human Ca2+ receptor, identified in a subject with autosomal dominant hypocalcemia, was found to cause a constitutive activation while at the same time lowering the maximal respons