-
1
-
-
0026003074
-
Activating mutations of the stimulatory G protein in the McCune-Albright syndrome
-
Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome. N Engl J Med 1991;325:1688-95.
-
(1991)
N Engl J Med
, vol.325
, pp. 1688-1695
-
-
Weinstein, L.S.1
Shenker, A.2
Gejman, P.V.3
Merino, M.J.4
Friedman, E.5
Spiegel, A.M.6
-
2
-
-
35148856270
-
The spectrum of McCune Albright syndrome
-
Zacharin M. The spectrum of McCune Albright syndrome. Pediatr Endocrinol Rev 2007;(4 Suppl 4):412-18.
-
(2007)
Pediatr Endocrinol Rev
, Issue.4 SUPPL. 4
, pp. 412-418
-
-
Zacharin, M.1
-
3
-
-
13644254142
-
Paediatric management of endocrine complications in McCune-Albright syndrome
-
Zacharin M. Paediatric management of endocrine complications in McCune-Albright syndrome. J Pediatr Endocrinol Metab 2005;18:33-41.
-
(2005)
J Pediatr Endocrinol Metab
, vol.18
, pp. 33-41
-
-
Zacharin, M.1
-
4
-
-
0028323562
-
An unusual presentation of McCune-Albright syndrome confirmed by an activating mutation of the Gs alpha-subunit from a bone lesion
-
Malchoff CD, Reardon G, MacGillivray DC, Yamase H, Rogol AD, Malchoff DM. An unusual presentation of McCune-Albright syndrome confirmed by an activating mutation of the Gs alpha-subunit from a bone lesion. J Clin Endocrinol Metab 1994;78:803-6.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 803-806
-
-
Malchoff, C.D.1
Reardon, G.2
MacGillivray, D.C.3
Yamase, H.4
Rogol, A.D.5
Malchoff, D.M.6
-
5
-
-
0015834582
-
Isolation of high-molecular-weight DNA from mammalian cells
-
Gross-Bellard M, Oudet P, Chambon P. Isolation of high-molecular-weight DNA from mammalian cells. Eur J Biochem 1973;36:32-8.
-
(1973)
Eur J Biochem
, vol.36
, pp. 32-38
-
-
Gross-Bellard, M.1
Oudet, P.2
Chambon, P.3
-
6
-
-
33749454373
-
An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus
-
Chow E, Meldrum CJ, Crooks R, Macrae F, Spigelman AD, Scott RJ. An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus. Clin Genet 2006;70:409-14.
-
(2006)
Clin Genet
, vol.70
, pp. 409-414
-
-
Chow, E.1
Meldrum, C.J.2
Crooks, R.3
Macrae, F.4
Spigelman, A.D.5
Scott, R.J.6
-
7
-
-
0031974516
-
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
-
Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, Müller O, Back W, Zimmer M. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat Genet 1998;18:38-43.
-
(1998)
Nat Genet
, vol.18
, pp. 38-43
-
-
Jenne, D.E.1
Reimann, H.2
Nezu, J.3
Friedel, W.4
Loff, S.5
Jeschke, R.6
Müller, O.7
Back, W.8
Zimmer, M.9
-
8
-
-
0030779964
-
Polymerase chain reaction-based technique for the selective enrichment and analysis of mosaic arg201 mutations in G alpha s from patients with fibrous dysplasia of bone
-
Candeliere GA, Roughley PJ, Glorieux FH. Polymerase chain reaction-based technique for the selective enrichment and analysis of mosaic arg201 mutations in G alpha s from patients with fibrous dysplasia of bone. Bone 1997;21:201-6.
-
(1997)
Bone
, vol.21
, pp. 201-206
-
-
Candeliere, G.A.1
Roughley, P.J.2
Glorieux, F.H.3
-
9
-
-
0015191808
-
Albright's syndrome-thirty years later. (Polyostotic fibrous dysplasia)
-
MacMahon HE. Albright's syndrome-thirty years later. (Polyostotic fibrous dysplasia). Pathol Annu 1971;6:81-146.
-
(1971)
Pathol Annu
, vol.6
, pp. 81-146
-
-
MacMahon, H.E.1
-
11
-
-
3142679707
-
McCune-Albright syndrome associated with pituitary microadenoma: patient report
-
Chen CJ, Liu JY, Cheng SN, Chang FW, Yuh YS. McCune-Albright syndrome associated with pituitary microadenoma: patient report. J Pediatr Endocrinol Metab 2004;17:365-9.
-
(2004)
J Pediatr Endocrinol Metab
, vol.17
, pp. 365-369
-
-
Chen, C.J.1
Liu, J.Y.2
Cheng, S.N.3
Chang, F.W.4
Yuh, Y.S.5
-
12
-
-
0030739305
-
Hyperthyroidism in McCune-Albright syndrome with a review of thyroid abnormalities sixty years after the first report
-
Mastorakos G, Mitsiades NS, Doufas AG, Koutras DA. Hyperthyroidism in McCune-Albright syndrome with a review of thyroid abnormalities sixty years after the first report. Thyroid 1997;7:433-9.
-
(1997)
Thyroid
, vol.7
, pp. 433-439
-
-
Mastorakos, G.1
Mitsiades, N.S.2
Doufas, A.G.3
Koutras, D.A.4
-
13
-
-
0033504785
-
Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome
-
Kirk JM, Brain CE, Carson DJ, Hyde JC, Grant DB. Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome. J Pediatr 1999;134:789-92.
-
(1999)
J Pediatr
, vol.134
, pp. 789-792
-
-
Kirk, J.M.1
Brain, C.E.2
Carson, D.J.3
Hyde, J.C.4
Grant, D.B.5
-
14
-
-
7444264668
-
Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males
-
Wasniewska M, De Luca F, Bertelloni S, Matarazzo P, Weber g, Crisafulli g, Valenzise M, Lala R. Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males. J Pediatr 2004;145:670-2.
-
(2004)
J Pediatr
, vol.145
, pp. 670-672
-
-
Wasniewska, M.1
De Luca, F.2
Bertelloni, S.3
Matarazzo, P.4
Weber, G.5
Crisafulli, G.6
Valenzise, M.7
Lala, R.8
-
15
-
-
0024404145
-
GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours
-
Landis CA, Masters SB, Spada A, Pace AM, Bourne HR, Vallar L. GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours. Nature 1989;340:692-6.
-
(1989)
Nature
, vol.340
, pp. 692-696
-
-
Landis, C.A.1
Masters, S.B.2
Spada, A.3
Pace, A.M.4
Bourne, H.R.5
Vallar, L.6
-
16
-
-
0038030796
-
Cushing's syndrome secondary to adrenocorticotropinindependent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene
-
Fragoso MC, Domenice S, Latronico AC, Martin RM, Pereira MA, Zerbini MC, Lucon AM, Mendonca BB. Cushing's syndrome secondary to adrenocorticotropinindependent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene. J Clin Endocrinol Metab 2003;88:2147-51.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 2147-2151
-
-
Fragoso, M.C.1
Domenice, S.2
Latronico, A.C.3
Martin, R.M.4
Pereira, M.A.5
Zerbini, M.C.6
Lucon, A.M.7
Mendonca, B.B.8
-
17
-
-
0141452998
-
Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations
-
Collins MT, Sarlis NJ, Merino MJ, Monroe J, Crawford SE, Krakoff JA, Guthrie LC, Bonat S, Robey PG, Shenker A. Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations. J Clin Endocrinol Metab 2003;88:4413-17.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 4413-4417
-
-
Collins, M.T.1
Sarlis, N.J.2
Merino, M.J.3
Monroe, J.4
Crawford, S.E.5
Krakoff, J.A.6
Guthrie, L.C.7
Bonat, S.8
Robey, P.G.9
Shenker, A.10
-
18
-
-
0030830109
-
Recurrent ovarian cyst and mutation of the Gs alpha gene in ovarian cyst fluid cells: what is the link with McCune-Albright syndrome?
-
Pienkowski C, Lumbroso S, Bieth E, Sultan C, Rochiccioli P, Tauber M. Recurrent ovarian cyst and mutation of the Gs alpha gene in ovarian cyst fluid cells: what is the link with McCune-Albright syndrome? Acta Paediatr 1997;86:1019-21.
-
(1997)
Acta Paediatr
, vol.86
, pp. 1019-1021
-
-
Pienkowski, C.1
Lumbroso, S.2
Bieth, E.3
Sultan, C.4
Rochiccioli, P.5
Tauber, M.6
-
19
-
-
34347391261
-
CREB-a real culprit in oncogenesis
-
Siu YT, Jin DY. CREB-a real culprit in oncogenesis. FEBS J 2007;274:3224-32.
-
(2007)
FEBS J
, vol.274
, pp. 3224-3232
-
-
Siu, Y.T.1
Jin, D.Y.2
-
20
-
-
19144366774
-
Risk of colorectal neoplasm in patients with acromegaly and its relationship with serum growth hormone levels
-
Matano Y, Okada T, Suzuki A, Yoneda T, Takeda Y, Mabuchi H. Risk of colorectal neoplasm in patients with acromegaly and its relationship with serum growth hormone levels. Am J Gastroenterol 2005;100:1154-60.
-
(2005)
Am J Gastroenterol
, vol.100
, pp. 1154-1160
-
-
Matano, Y.1
Okada, T.2
Suzuki, A.3
Yoneda, T.4
Takeda, Y.5
Mabuchi, H.6
|