The PTH/PTHrP receptor in Jansen's metaphyseal chondrodysplasia

被引:25
作者
Calvi, LM
Schipani, E [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Endocrine Unit, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
关键词
D O I
10.1007/BF03343773
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:545 / 554
页数:10
相关论文
共 64 条
[1]   EXPRESSION CLONING OF A COMMON RECEPTOR FOR PARATHYROID-HORMONE AND PARATHYROID HORMONE-RELATED PEPTIDE FROM RAT OSTEOBLAST-LIKE CELLS - A SINGLE RECEPTOR STIMULATES INTRACELLULAR ACCUMULATION OF BOTH CAMP AND INOSITOL TRISPHOSPHATES AND INCREASES INTRACELLULAR FREE CALCIUM [J].
ABOUSAMRA, AB ;
JUPPNER, H ;
FORCE, T ;
FREEMAN, MW ;
KONG, XF ;
SCHIPANI, E ;
URENA, P ;
RICHARDS, J ;
BONVENTRE, JV ;
POTTS, JT ;
KRONENBERG, HM ;
SEGRE, GV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :2732-2736
[2]  
[Anonymous], 1997, Metabolic Bone Disease
[3]   OSTEOBLAST AND CHONDROBLAST DIFFERENTIATION [J].
AUBIN, JE ;
LIU, F ;
MALAVAL, L ;
GUPTA, AK .
BONE, 1995, 17 (02) :S77-S83
[4]   Mutations in the Ca2+-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism [J].
Baron, J ;
Winer, KK ;
Yanovski, JA ;
Cunningham, AW ;
Laue, L ;
Zimmerman, D ;
Cutler, GB .
HUMAN MOLECULAR GENETICS, 1996, 5 (05) :601-606
[5]   Expression of the parathyroid hormone receptor and correlation with other osteoblastic parameters in fetal rat osteoblasts [J].
Bos, MP ;
vanderMeer, JM ;
Feyen, JHM ;
HerrmannErlee, MPM .
CALCIFIED TISSUE INTERNATIONAL, 1996, 58 (02) :95-100
[6]  
BROADUS A, 1994, PARATHYROIDS BASIC C, P311
[7]   THE JANSEN TYPE OF METAPHYSEAL CHONDRODYSPLASIA - CONFIRMATION OF DOMINANT INHERITANCE AND REVIEW OF RADIOGRAPHIC MANIFESTATIONS IN THE NEWBORN AND ADULT [J].
CHARROW, J ;
POZNANSKI, AK .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (02) :321-327
[8]   The parathyroid hormone parathyroid hormone-related peptide receptor coordinates endochondral bone development by directly controlling chondrocyte differentiation [J].
Chung, UI ;
Lanske, B ;
Lee, KC ;
Li, E ;
Kronenberg, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13030-13035
[9]  
de Haas W H, 1969, J Bone Joint Surg Br, V51, P290
[10]   HETEROZYGOUS MISSENSE MUTATION IN THE RHODOPSIN GENE AS A CAUSE OF CONGENITAL STATIONARY NIGHT BLINDNESS [J].
DRYJA, TP ;
BERSON, EL ;
RAO, VR ;
OPRIAN, DD .
NATURE GENETICS, 1993, 4 (03) :280-283