-
1
-
-
33748966446
-
Role of calcium-sensing receptor in mineral ion metabolism and inherited disorders of calcium-sensing
-
Chattopadhyay N, Brown EM: Role of calcium-sensing receptor in mineral ion metabolism and inherited disorders of calcium-sensing. Mol Genet Metab 2006; 89: 189-202.
-
(2006)
Mol Genet Metab
, vol.89
, pp. 189-202
-
-
Chattopadhyay, N.1
Brown, E.M.2
-
2
-
-
1442277000
-
Diseases associated with the extracellular calcium-sensing receptor
-
Thakker RV: Diseases associated with the extracellular calcium-sensing receptor. Cell Calcium 2004; 35: 275-282.
-
(2004)
Cell Calcium
, vol.35
, pp. 275-282
-
-
Thakker, R.V.1
-
3
-
-
0024422565
-
Familial benign (hypocalciuric) hypercalcemia. A troublesome mimic of mild primary hyperparathyroidism
-
Heath 3rd H: Familial benign (hypocalciuric) hypercalcemia. A troublesome mimic of mild primary hyperparathyroidism. Endocrinol Metab Clin North Am 1989; 18: 723-740.
-
(1989)
Endocrinol Metab Clin North Am
, vol.18
, pp. 723-740
-
-
Heath III, H.1
-
4
-
-
0030453451
-
Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis
-
Pearce SH, Wooding C, Davies M et al: Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis. Clin Endocrinol (Oxf) 1996; 45: 675-680.
-
(1996)
Clin Endocrinol (Oxf)
, vol.45
, pp. 675-680
-
-
Pearce, S.H.1
Wooding, C.2
Davies, M.3
-
5
-
-
0027787680
-
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyper-parathyroidism
-
Pollak MR, Brown EM, Chou YH et al: Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyper-parathyroidism. Cell 1993; 75: 1297-1303.
-
(1993)
Cell
, vol.75
, pp. 1297-1303
-
-
Pollak, M.R.1
Brown, E.M.2
Chou, Y.H.3
-
6
-
-
18744429143
-
The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families
-
Chou YH, Brown EM, Levi T et al: The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families. Nat Genet 1992; 1: 295-300.
-
(1992)
Nat Genet
, vol.1
, pp. 295-300
-
-
Chou, Y.H.1
Brown, E.M.2
Levi, T.3
-
7
-
-
0029967961
-
Functional characterization of calcium-sensing receptor mutations expressed in human embryonic kidney cells
-
Pearce SH, Bai M, Quinn SJ et al: Functional characterization of calcium-sensing receptor mutations expressed in human embryonic kidney cells. J Clin Invest 1996; 98: 1860-1866.
-
(1996)
J Clin Invest
, vol.98
, pp. 1860-1866
-
-
Pearce, S.H.1
Bai, M.2
Quinn, S.J.3
-
8
-
-
28244475075
-
The gene repertoire and the common evolutionary history of glutamate, pheromone (V2R), taste(1) and other related G protein-coupled receptors
-
Bjarnadottir TK, Fredriksson R, Schioth HB: The gene repertoire and the common evolutionary history of glutamate, pheromone (V2R), taste(1) and other related G protein-coupled receptors. Gene 2005; 362: 70-84.
-
(2005)
Gene
, vol.362
, pp. 70-84
-
-
Bjarnadottir, T.K.1
Fredriksson, R.2
Schioth, H.B.3
-
9
-
-
0038125588
-
Extracellular calcium sensing and signalling
-
Hofer AM, Brown EM: Extracellular calcium sensing and signalling. Nat Rev Mol Cell Biol 2003; 4: 530-538.
-
(2003)
Nat Rev Mol Cell Biol
, vol.4
, pp. 530-538
-
-
Hofer, A.M.1
Brown, E.M.2
-
10
-
-
0028037143
-
Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation
-
Pollak MR, Brown EM, Estep HL et al: Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation. Nat Genet 1994; 8: 303-307.
-
(1994)
Nat Genet
, vol.8
, pp. 303-307
-
-
Pollak, M.R.1
Brown, E.M.2
Estep, H.L.3
-
11
-
-
10144256536
-
A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor
-
Pearce SH, Williamson C, Kifor O et al: A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor. N Engl J Med 1996; 335: 1115-1122.
-
(1996)
N Engl J Med
, vol.335
, pp. 1115-1122
-
-
Pearce, S.H.1
Williamson, C.2
Kifor, O.3
-
12
-
-
0037469737
-
Activation of the MAP kinase cascade by exogenous calcium-sensing receptor
-
Hobson SA, Wright J, Lee F et al: Activation of the MAP kinase cascade by exogenous calcium-sensing receptor. Mol Cell Endocrinol 2003; 200: 189-198.
-
(2003)
Mol Cell Endocrinol
, vol.200
, pp. 189-198
-
-
Hobson, S.A.1
Wright, J.2
Lee, F.3
-
13
-
-
37349016937
-
Familial isolated primary hyperparathyroid-ism caused by mutations of the MEN1 gene
-
Hannan FM, Nesbit MA, Christie PT et al: Familial isolated primary hyperparathyroid-ism caused by mutations of the MEN1 gene. Nat Clin Pract Endocrinol Metab 2008; 4: 53-58.
-
(2008)
Nat Clin Pract Endocrinol Metab
, vol.4
, pp. 53-58
-
-
Hannan, F.M.1
Nesbit, M.A.2
Christie, P.T.3
-
14
-
-
0036959850
-
Identification and functional characterization of novel calcium-sensing receptor mutations in familial hypocalciuric hypercalcemia and autosomal dominant hypocalcemia
-
D'Souza-Li L, Yang B, Canaff L et al: Identification and functional characterization of novel calcium-sensing receptor mutations in familial hypocalciuric hypercalcemia and autosomal dominant hypocalcemia. J Clin Endocrinol Metab 2002; 87: 1309-1318.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 1309-1318
-
-
D'Souza-Li, L.1
Yang, B.2
Canaff, L.3
-
15
-
-
0027517161
-
Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: Evidence for locus heterogeneity
-
Heath 3rd H, Jackson CE, Otterud B et al: Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity. Am J Hum Genet 1993; 53: 193-200.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 193-200
-
-
Heath III, H.1
Jackson, C.E.2
Otterud, B.3
-
16
-
-
0026732656
-
Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemia
-
McMurtry CT, Schranck FW, Walkenhorst DA et al: Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemia. Am J Med 1992; 93: 247-258.
-
(1992)
Am J Med
, vol.93
, pp. 247-258
-
-
McMurtry, C.T.1
Schranck, F.W.2
Walkenhorst, D.A.3
-
17
-
-
0033366514
-
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13
-
Lloyd SE, Pannett AA, Dixon PH et al: Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13. Am J Hum Genet 1999; 64: 189-195.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 189-195
-
-
Lloyd, S.E.1
Pannett, A.A.2
Dixon, P.H.3
-
18
-
-
0029073170
-
Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH
-
Trump D, Whyte MP, Wooding C et al: Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH. Hum Genet 1995; 96: 183-187.
-
(1995)
Hum Genet
, vol.96
, pp. 183-187
-
-
Trump, D.1
Whyte, M.P.2
Wooding, C.3
-
19
-
-
0028866218
-
An integrated metric physical map of human chromosome 19
-
Ashworth LK, Batzer MA, Brandriff B et al: An integrated metric physical map of human chromosome 19. Nat Genet 1995; 11: 422-427.
-
(1995)
Nat Genet
, vol.11
, pp. 422-427
-
-
Ashworth, L.K.1
Batzer, M.A.2
Brandriff, B.3
-
20
-
-
0028231090
-
The 1993-1994 Genethon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A et al: The 1993-1994 Genethon human genetic linkage map. Nat Genet 1994; 7: 246-339.
-
(1994)
Nat Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
-
21
-
-
1842536305
-
The DNA sequence and biology of human chromosome 19
-
Grimwood J, Gordon LA, Olsen A et al: The DNA sequence and biology of human chromosome 19. Nature 2004; 428: 529-535.
-
(2004)
Nature
, vol.428
, pp. 529-535
-
-
Grimwood, J.1
Gordon, L.A.2
Olsen, A.3
-
23
-
-
38549092091
-
Database resources of the National Center for Biotechnology Information
-
Wheeler DL, Barrett T, Benson DA et al: Database resources of the National Center for Biotechnology Information. Nucleic Acids Res 2008; 36: D13-D21.
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Wheeler, D.L.1
Barrett, T.2
Benson, D.A.3
-
24
-
-
26444453686
-
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypopar-athyroidism
-
Bowl MR, Nesbit MA, Harding B et al: An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypopar-athyroidism. J Clin Invest 2005; 115: 2822-2831.
-
(2005)
J Clin Invest
, vol.115
, pp. 2822-2831
-
-
Bowl, M.R.1
Nesbit, M.A.2
Harding, B.3
-
25
-
-
0026865130
-
A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism
-
Parkinson DB, Thakker RV: A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism. Nat Genet 1992; 1: 149-152.
-
(1992)
Nat Genet
, vol.1
, pp. 149-152
-
-
Parkinson, D.B.1
Thakker, R.V.2
-
26
-
-
0030724008
-
Identification of putative transmembrane receptor sequences homologous to the calcium-sensing G-protein-coupled receptor
-
Hinson TK, Damodaran TV, Chen J et al: Identification of putative transmembrane receptor sequences homologous to the calcium-sensing G-protein-coupled receptor. Genomics 1997; 45: 279-289.
-
(1997)
Genomics
, vol.45
, pp. 279-289
-
-
Hinson, T.K.1
Damodaran, T.V.2
Chen, J.3
-
27
-
-
23244440415
-
Composition and evolution of the V2r vomeronasal receptor gene repertoire in mice and rats
-
Yang H, Shi P, Zhang YP et al: Composition and evolution of the V2r vomeronasal receptor gene repertoire in mice and rats. Genomics 2005; 86: 306-315.
-
(2005)
Genomics
, vol.86
, pp. 306-315
-
-
Yang, H.1
Shi, P.2
Zhang, Y.P.3
-
28
-
-
0030219837
-
Detailed comparative map of human chromosome 19q and related regions of the mouse genome
-
Stubbs L, Carver EA, Shannon ME et al: Detailed comparative map of human chromosome 19q and related regions of the mouse genome. Genomics 1996; 35: 499-508.
-
(1996)
Genomics
, vol.35
, pp. 499-508
-
-
Stubbs, L.1
Carver, E.A.2
Shannon, M.E.3
-
29
-
-
0038336902
-
Centrally administered tuberoinfundibular peptide of 39 residues inhibits arginine vasopressin release in conscious rats
-
Sugimura Y, Murase T, Ishizaki S et al: Centrally administered tuberoinfundibular peptide of 39 residues inhibits arginine vasopressin release in conscious rats. Endocrinology 2003; 144: 2791-2796.
-
(2003)
Endocrinology
, vol.144
, pp. 2791-2796
-
-
Sugimura, Y.1
Murase, T.2
Ishizaki, S.3
-
30
-
-
34249307514
-
Arginine (CGC) codon targeting in the human prostacyclin receptor gene (PTGIR) and G-protein coupled receptors (GPCR)
-
Stitham J, Arehart EJ, Gleim S et al: Arginine (CGC) codon targeting in the human prostacyclin receptor gene (PTGIR) and G-protein coupled receptors (GPCR). Gene 2007; 396: 180-187.
-
(2007)
Gene
, vol.396
, pp. 180-187
-
-
Stitham, J.1
Arehart, E.J.2
Gleim, S.3
-
31
-
-
15944413784
-
Distinction in gene expression profiles demonstrated in parathyroid adenomas by high-density oligoarray technology
-
Forsberg L, Bjorck E, Hashemi J et al: Distinction in gene expression profiles demonstrated in parathyroid adenomas by high-density oligoarray technology. Eur J Endocrinol 2005; 152: 459-470.
-
(2005)
Eur J Endocrinol
, vol.152
, pp. 459-470
-
-
Forsberg, L.1
Bjorck, E.2
Hashemi, J.3
-
32
-
-
34249656324
-
Sphingosine kinase type 2 activation by ERK-mediated phosphorylation
-
Hait NC, Bellamy A, Milstien S et al: Sphingosine kinase type 2 activation by ERK-mediated phosphorylation. J Biol Chem 2007; 282: 12058-12065.
-
(2007)
J Biol Chem
, vol.282
, pp. 12058-12065
-
-
Hait, N.C.1
Bellamy, A.2
Milstien, S.3
-
34
-
-
0036843752
-
Calnuc an EF-hand Ca(2+)-binding protein, is stored and processed in the Golgi and secreted by the constitutive-like pathway in AtT20 cells
-
Lavoie C, Meerloo T, Lin P et al: Calnuc, an EF-hand Ca(2+)-binding protein, is stored and processed in the Golgi and secreted by the constitutive-like pathway in AtT20 cells. Mol Endocrinol 2002; 16: 2462-2474.
-
(2002)
Mol Endocrinol
, vol.16
, pp. 2462-2474
-
-
Lavoie, C.1
Meerloo, T.2
Lin, P.3
-
35
-
-
34548436576
-
Histidine-rich Ca-binding protein interacts with sarcoplasmic reticulum Ca-ATPase
-
Arvanitis DA, Vafiadaki E, Fan GC et al: Histidine-rich Ca-binding protein interacts with sarcoplasmic reticulum Ca-ATPase. Am J Physiol Heart Circ Physiol 2007; 293: H1581-H1589.
-
(2007)
Am J Physiol Heart Circ Physiol
, vol.293
-
-
Arvanitis, D.A.1
Vafiadaki, E.2
Fan, G.C.3
-
36
-
-
33646772541
-
A proteomic approach reveals transient association of reticulocalbin-3, a novel member of the CREC family, with the precursor of subtilisin-like proprotein convertase, PACE4
-
Tsuji A, Kikuchi Y, Sato Y et al: A proteomic approach reveals transient association of reticulocalbin-3, a novel member of the CREC family, with the precursor of subtilisin-like proprotein convertase, PACE4. Biochem J 2006; 396: 51-59.
-
(2006)
Biochem J
, vol.396
, pp. 51-59
-
-
Tsuji, A.1
Kikuchi, Y.2
Sato, Y.3
-
37
-
-
34548246116
-
The calcium-sensing receptor changes cell shape via a beta-arrestin-1 ARNO ARF6 ELMO protein network
-
Bouschet T, Martin S, Kanamarlapudi V et al: The calcium-sensing receptor changes cell shape via a beta-arrestin-1 ARNO ARF6 ELMO protein network. J Cell Sci 2007; 120: 2489-2497.
-
(2007)
J Cell Sci
, vol.120
, pp. 2489-2497
-
-
Bouschet, T.1
Martin, S.2
Kanamarlapudi, V.3
-
38
-
-
34447622294
-
Ras effector pathways modulate scatter factor-stimulated NF-kappaB signaling and protection against DNA damage
-
Fan S, Meng Q, Laterra JJ et al: Ras effector pathways modulate scatter factor-stimulated NF-kappaB signaling and protection against DNA damage. Oncogene 2007; 26: 4774-4796.
-
(2007)
Oncogene
, vol.26
, pp. 4774-4796
-
-
Fan, S.1
Meng, Q.2
Laterra, J.J.3
-
39
-
-
21744434727
-
Chromosomal rearrangements are associated with higher rates of molecular evolution in mammals
-
Marques-Bonet T, Navarro A: Chromosomal rearrangements are associated with higher rates of molecular evolution in mammals. Gene 2005; 353: 147-154.
-
(2005)
Gene
, vol.353
, pp. 147-154
-
-
Marques-Bonet, T.1
Navarro, A.2
|