-
1
-
-
33846429183
-
Clinical lessons from the calcium-sensing receptor
-
Brown EM Clinical lessons from the calcium-sensing receptor. Nat Clin Pract Endocrinol Metab 2007, 3(2):122-133.
-
(2007)
Nat Clin Pract Endocrinol Metab
, vol.3
, Issue.2
, pp. 122-133
-
-
Brown, E.M.1
-
2
-
-
33748462857
-
The diagnosis and management of asymptomatic primary hyperparathyroidism
-
Silverberg SJ, Bilezikian JP The diagnosis and management of asymptomatic primary hyperparathyroidism. Nat Clin Pract Endocrinol Metab 2006, 2(9):494-503.
-
(2006)
Nat Clin Pract Endocrinol Metab
, vol.2
, Issue.9
, pp. 494-503
-
-
Silverberg, S.J.1
Bilezikian, J.P.2
-
3
-
-
0035097021
-
Clinical review 122: parathyroid carcinoma
-
Shane E Clinical review 122: parathyroid carcinoma. J Clin Endocrinol Metab 2001, 86(2):485-493.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, Issue.2
, pp. 485-493
-
-
Shane, E.1
-
4
-
-
1642367247
-
The parathyroid glands
-
Churchill Livingstone, Philadelphia, V. LiVolsi, S. Asa (Eds.)
-
Apel RL, Asa SL The parathyroid glands. Endocrine Pathology 2002, 103-147. Churchill Livingstone, Philadelphia. V. LiVolsi, S. Asa (Eds.).
-
(2002)
Endocrine Pathology
, pp. 103-147
-
-
Apel, R.L.1
Asa, S.L.2
-
5
-
-
0034700450
-
Hyperparathyroid and hypoparathyroid disorders
-
Marx SJ Hyperparathyroid and hypoparathyroid disorders. N Engl J Med 2000, 343(25):1863-1875.
-
(2000)
N Engl J Med
, vol.343
, Issue.25
, pp. 1863-1875
-
-
Marx, S.J.1
-
6
-
-
85047682409
-
Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
Brandi ML, Gagel RF, Angeli A, Bilezikian JP, Beck-Peccoz P, Bordi C, et al. Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 2001, 86(12):5658-5671.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, Issue.12
, pp. 5658-5671
-
-
Brandi, M.L.1
Gagel, R.F.2
Angeli, A.3
Bilezikian, J.P.4
Beck-Peccoz, P.5
Bordi, C.6
-
7
-
-
0030963446
-
Positional cloning of the gene for multiple endocrine neoplasia-type 1
-
Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, et al. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science 1997, 276(5311):404-407.
-
(1997)
Science
, vol.276
, Issue.5311
, pp. 404-407
-
-
Chandrasekharappa, S.C.1
Guru, S.C.2
Manickam, P.3
Olufemi, S.E.4
Collins, F.S.5
Emmert-Buck, M.R.6
-
8
-
-
13844318139
-
Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory
-
Klein RD, Salih S, Bessoni J, Bale AE Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory. Genet Med 2005, 7(2):131-138.
-
(2005)
Genet Med
, vol.7
, Issue.2
, pp. 131-138
-
-
Klein, R.D.1
Salih, S.2
Bessoni, J.3
Bale, A.E.4
-
9
-
-
13444304438
-
Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing
-
Ellard S, Hattersley AT, Brewer CM, Vaidya B Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing. Clin Endocrinol (Oxf) 2005, 62(2):169-175.
-
(2005)
Clin Endocrinol (Oxf)
, vol.62
, Issue.2
, pp. 169-175
-
-
Ellard, S.1
Hattersley, A.T.2
Brewer, C.M.3
Vaidya, B.4
-
10
-
-
0041777670
-
Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients
-
Cebrian A, Ruiz-Llorente S, Cascon A, Pollan M, Diez JJ, Pico A, et al. Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients. J Med Genet 2003, 40(5):e72.
-
(2003)
J Med Genet
, vol.40
, Issue.5
-
-
Cebrian, A.1
Ruiz-Llorente, S.2
Cascon, A.3
Pollan, M.4
Diez, J.J.5
Pico, A.6
-
11
-
-
0038434530
-
Multiple endocrine neoplasia type 1 (MEN1): genetic and clinical analysis in the Southern Chinese
-
Tso AW, Rong R, Lo CY, Tan KC, Tiu SC, Wat NM, et al. Multiple endocrine neoplasia type 1 (MEN1): genetic and clinical analysis in the Southern Chinese. Clin Endocrinol (Oxf) 2003, 59(1):129-135.
-
(2003)
Clin Endocrinol (Oxf)
, vol.59
, Issue.1
, pp. 129-135
-
-
Tso, A.W.1
Rong, R.2
Lo, C.Y.3
Tan, K.C.4
Tiu, S.C.5
Wat, N.M.6
-
12
-
-
0032900482
-
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases
-
Poncin J, Abs R, Velkeniers B, Bonduelle M, Abramowicz M, Legros JJ, et al. Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases. Hum Mutat 1999, 13(1):54-60.
-
(1999)
Hum Mutat
, vol.13
, Issue.1
, pp. 54-60
-
-
Poncin, J.1
Abs, R.2
Velkeniers, B.3
Bonduelle, M.4
Abramowicz, M.5
Legros, J.J.6
-
13
-
-
0032756819
-
Screening for MEN1 mutations in patients with atypical endocrine neoplasia
-
discussion 103-4.
-
Dackiw AP, Cote GJ, Fleming JB, Schultz PN, Stanford P, Vassilopoulou-Sellin R, et al. Screening for MEN1 mutations in patients with atypical endocrine neoplasia. Surgery 1999, 126(6):1097-1103. discussion 103-4.
-
(1999)
Surgery
, vol.126
, Issue.6
, pp. 1097-1103
-
-
Dackiw, A.P.1
Cote, G.J.2
Fleming, J.B.3
Schultz, P.N.4
Stanford, P.5
Vassilopoulou-Sellin, R.6
-
14
-
-
0033774112
-
Identification of MEN1 gene mutations in families with MEN 1 and related disorders
-
Bergman L, Teh B, Cardinal J, Palmer J, Walters M, Shepherd J, et al. Identification of MEN1 gene mutations in families with MEN 1 and related disorders. Br J Cancer 2000, 83(8):1009-1014.
-
(2000)
Br J Cancer
, vol.83
, Issue.8
, pp. 1009-1014
-
-
Bergman, L.1
Teh, B.2
Cardinal, J.3
Palmer, J.4
Walters, M.5
Shepherd, J.6
-
15
-
-
0007756054
-
Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1
-
Hai N, Aoki N, Shimatsu A, Mori T, Kosugi S Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1. Clin Endocrinol (Oxf) 2000, 52(4):509-518.
-
(2000)
Clin Endocrinol (Oxf)
, vol.52
, Issue.4
, pp. 509-518
-
-
Hai, N.1
Aoki, N.2
Shimatsu, A.3
Mori, T.4
Kosugi, S.5
-
16
-
-
34249860559
-
The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations
-
Ozawa A, Agarwal SK, Mateo CM, Burns AL, Rice TS, Kennedy PA, et al. The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations. J Clin Endocrinol Metab 2007, 92(5):1948-1951.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, Issue.5
, pp. 1948-1951
-
-
Ozawa, A.1
Agarwal, S.K.2
Mateo, C.M.3
Burns, A.L.4
Rice, T.S.5
Kennedy, P.A.6
-
17
-
-
0036606022
-
Recessive transmission of a multiple endocrine neoplasia syndrome in the rat
-
Fritz A, Walch A, Piotrowska K, Rosemann M, Schaffer E, Weber K, et al. Recessive transmission of a multiple endocrine neoplasia syndrome in the rat. Cancer Res 2002, 62(11):3048-3051.
-
(2002)
Cancer Res
, vol.62
, Issue.11
, pp. 3048-3051
-
-
Fritz, A.1
Walch, A.2
Piotrowska, K.3
Rosemann, M.4
Schaffer, E.5
Weber, K.6
-
18
-
-
33750361636
-
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans
-
Pellegata NS, Quintanilla-Martinez L, Siggelkow H, Samson E, Bink K, Hofler H, et al. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci U S A 2006, 103(42):15558-15563.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, Issue.42
, pp. 15558-15563
-
-
Pellegata, N.S.1
Quintanilla-Martinez, L.2
Siggelkow, H.3
Samson, E.4
Bink, K.5
Hofler, H.6
-
19
-
-
77956581284
-
MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations.
-
Georgitsi M, MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations. Best Pract Res Clin Endocrinol Metab. 24(3):425-37.
-
Best Pract Res Clin Endocrinol Metab.
, vol.24
, Issue.3
-
-
Georgitsi, M.1
-
20
-
-
66849137159
-
Rare germline mutations in cyclin-dependent kinase inhibitor genes in MEN1 and related states
-
Agarwal SK, Mateo CM, Marx SJ Rare germline mutations in cyclin-dependent kinase inhibitor genes in MEN1 and related states. J Clin Endocrinol Metab 2009.
-
(2009)
J Clin Endocrinol Metab
-
-
Agarwal, S.K.1
Mateo, C.M.2
Marx, S.J.3
-
21
-
-
78650184526
-
Update multiple endocrine neoplasia type 2
-
Raue F, Frank-Raue K Update multiple endocrine neoplasia type 2. Fam Cancer 2010, 9(3):449-457.
-
(2010)
Fam Cancer
, vol.9
, Issue.3
, pp. 449-457
-
-
Raue, F.1
Frank-Raue, K.2
-
23
-
-
0032894774
-
RET proto-oncogene in the development of human cancer
-
Eng C RET proto-oncogene in the development of human cancer. J Clin Oncol 1999, 17(1):380-393.
-
(1999)
J Clin Oncol
, vol.17
, Issue.1
, pp. 380-393
-
-
Eng, C.1
-
24
-
-
31544434233
-
Polymorphisms in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A
-
Lesueur F, Cebrian A, Robledo M, Niccoli-Sire P, Svensson KA, Pinson S, et al. Polymorphisms in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A. Cancer Res 2006, 66(2):1177-1180.
-
(2006)
Cancer Res
, vol.66
, Issue.2
, pp. 1177-1180
-
-
Lesueur, F.1
Cebrian, A.2
Robledo, M.3
Niccoli-Sire, P.4
Svensson, K.A.5
Pinson, S.6
-
25
-
-
19944434120
-
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome
-
Bradley KJ, Hobbs MR, Buley ID, Carpten JD, Cavaco BM, Fares JE, et al. Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. J Intern Med 2005, 257(1):18-26.
-
(2005)
J Intern Med
, vol.257
, Issue.1
, pp. 18-26
-
-
Bradley, K.J.1
Hobbs, M.R.2
Buley, I.D.3
Carpten, J.D.4
Cavaco, B.M.5
Fares, J.E.6
-
26
-
-
15144343105
-
Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families
-
Teh BT, Farnebo F, Twigg S, Hoog A, Kytola S, Korpi-Hyovalti E, et al. Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families. J Clin Endocrinol Metab 1998, 83(6):2114-2120.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, Issue.6
, pp. 2114-2120
-
-
Teh, B.T.1
Farnebo, F.2
Twigg, S.3
Hoog, A.4
Kytola, S.5
Korpi-Hyovalti, E.6
-
27
-
-
0032899239
-
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31
-
Williamson C, Cavaco BM, Jauch A, Dixon PH, Forbes S, Harding B, et al. Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31. J Bone Miner Res 1999, 14(2):230-239.
-
(1999)
J Bone Miner Res
, vol.14
, Issue.2
, pp. 230-239
-
-
Williamson, C.1
Cavaco, B.M.2
Jauch, A.3
Dixon, P.H.4
Forbes, S.5
Harding, B.6
-
28
-
-
18744385803
-
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
-
Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 2002, 32(4):676-680.
-
(2002)
Nat Genet
, vol.32
, Issue.4
, pp. 676-680
-
-
Carpten, J.D.1
Robbins, C.M.2
Villablanca, A.3
Forsberg, L.4
Presciuttini, S.5
Bailey-Wilson, J.6
-
29
-
-
58249097267
-
Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism
-
Masi G, Barzon L, Iacobone M, Viel G, Porzionato A, Macchi V, et al. Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism. Endocr Relat Cancer 2008, 15(4):1115-1126.
-
(2008)
Endocr Relat Cancer
, vol.15
, Issue.4
, pp. 1115-1126
-
-
Masi, G.1
Barzon, L.2
Iacobone, M.3
Viel, G.4
Porzionato, A.5
Macchi, V.6
-
30
-
-
77149133985
-
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors
-
Newey PJ, Bowl MR, Cranston T, Thakker RV Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors. Hum Mutat 2010, 31(3):295-307.
-
(2010)
Hum Mutat
, vol.31
, Issue.3
, pp. 295-307
-
-
Newey, P.J.1
Bowl, M.R.2
Cranston, T.3
Thakker, R.V.4
-
31
-
-
0038332150
-
Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism
-
Pannett AA, Kennedy AM, Turner JJ, Forbes SA, Cavaco BM, Bassett JH, et al. Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. Clin Endocrinol (Oxf) 2003, 58(5):639-646.
-
(2003)
Clin Endocrinol (Oxf)
, vol.58
, Issue.5
, pp. 639-646
-
-
Pannett, A.A.1
Kennedy, A.M.2
Turner, J.J.3
Forbes, S.A.4
Cavaco, B.M.5
Bassett, J.H.6
-
32
-
-
33644943454
-
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours
-
Bradley KJ, Cavaco BM, Bowl MR, Harding B, Cranston T, Fratter C, et al. Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. Clin Endocrinol (Oxf) 2006, 64(3):299-306.
-
(2006)
Clin Endocrinol (Oxf)
, vol.64
, Issue.3
, pp. 299-306
-
-
Bradley, K.J.1
Cavaco, B.M.2
Bowl, M.R.3
Harding, B.4
Cranston, T.5
Fratter, C.6
-
33
-
-
33746855998
-
Familial isolated hyperparathyroidism is linked to a 1.7Mb region on chromosome 2p13.3-14
-
Warner JV, Nyholt DR, Busfield F, Epstein M, Burgess J, Stranks S, et al. Familial isolated hyperparathyroidism is linked to a 1.7Mb region on chromosome 2p13.3-14. J Med Genet 2006, 43(3):e12.
-
(2006)
J Med Genet
, vol.43
, Issue.3
-
-
Warner, J.V.1
Nyholt, D.R.2
Busfield, F.3
Epstein, M.4
Burgess, J.5
Stranks, S.6
-
34
-
-
40149084169
-
Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations
-
Egbuna OI, Brown EM Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations. Best Pract Res Clin Rheumatol 2008, 22(1):129-148.
-
(2008)
Best Pract Res Clin Rheumatol
, vol.22
, Issue.1
, pp. 129-148
-
-
Egbuna, O.I.1
Brown, E.M.2
-
35
-
-
0028220464
-
Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype
-
Pollak MR, Chou YH, Marx SJ, Steinmann B, Cole DE, Brandi ML, et al. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype. J Clin Invest 1994, 93(3):1108-1112.
-
(1994)
J Clin Invest
, vol.93
, Issue.3
, pp. 1108-1112
-
-
Pollak, M.R.1
Chou, Y.H.2
Marx, S.J.3
Steinmann, B.4
Cole, D.E.5
Brandi, M.L.6
-
36
-
-
0035522894
-
Two genetic hits (more or less) to cancer
-
Knudson AG Two genetic hits (more or less) to cancer. Nat Rev Cancer 2001, 1(2):157-162.
-
(2001)
Nat Rev Cancer
, vol.1
, Issue.2
, pp. 157-162
-
-
Knudson, A.G.1
-
37
-
-
0028204821
-
Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma
-
Cryns VL, Thor A, Xu HJ, Hu SX, Wierman ME, Vickery AL, et al. Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma. N Engl J Med 1994, 330(11):757-761.
-
(1994)
N Engl J Med
, vol.330
, Issue.11
, pp. 757-761
-
-
Cryns, V.L.1
Thor, A.2
Xu, H.J.3
Hu, S.X.4
Wierman, M.E.5
Vickery, A.L.6
-
38
-
-
0025183139
-
Genetic abnormalities in sporadic parathyroid adenomas
-
Friedman E, Bale AE, Marx SJ, Norton JA, Arnold A, Tu T, et al. Genetic abnormalities in sporadic parathyroid adenomas. J Clin Endocrinol Metab 1990, 71(2):293-297.
-
(1990)
J Clin Endocrinol Metab
, vol.71
, Issue.2
, pp. 293-297
-
-
Friedman, E.1
Bale, A.E.2
Marx, S.J.3
Norton, J.A.4
Arnold, A.5
Tu, T.6
-
39
-
-
0028946265
-
Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia
-
Arnold A, Brown MF, Urena P, Gaz RD, Sarfati E, Drueke TB Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia. J Clin Invest 1995, 95(5):2047-2053.
-
(1995)
J Clin Invest
, vol.95
, Issue.5
, pp. 2047-2053
-
-
Arnold, A.1
Brown, M.F.2
Urena, P.3
Gaz, R.D.4
Sarfati, E.5
Drueke, T.B.6
-
40
-
-
0030755071
-
Somatic mutation of the MEN1 gene in parathyroid tumours
-
Heppner C, Kester MB, Agarwal SK, Debelenko LV, Emmert-Buck MR, Guru SC, et al. Somatic mutation of the MEN1 gene in parathyroid tumours. Nat Genet 1997, 16(4):375-378.
-
(1997)
Nat Genet
, vol.16
, Issue.4
, pp. 375-378
-
-
Heppner, C.1
Kester, M.B.2
Agarwal, S.K.3
Debelenko, L.V.4
Emmert-Buck, M.R.5
Guru, S.C.6
-
41
-
-
0031759392
-
Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism
-
Carling T, Correa P, Hessman O, Hedberg J, Skogseid B, Lindberg D, et al. Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism. J Clin Endocrinol Metab 1998, 83(8):2960-2963.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, Issue.8
, pp. 2960-2963
-
-
Carling, T.1
Correa, P.2
Hessman, O.3
Hedberg, J.4
Skogseid, B.5
Lindberg, D.6
-
42
-
-
15144346400
-
Alterations of the MEN1 gene in sporadic parathyroid tumors
-
Farnebo F, Teh BT, Kytola S, Svensson A, Phelan C, Sandelin K, et al. Alterations of the MEN1 gene in sporadic parathyroid tumors. J Clin Endocrinol Metab 1998, 83(8):2627-2630.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, Issue.8
, pp. 2627-2630
-
-
Farnebo, F.1
Teh, B.T.2
Kytola, S.3
Svensson, A.4
Phelan, C.5
Sandelin, K.6
-
43
-
-
0037168952
-
Biallelic inactivation by somatic mutations of the MEN1 gene in sporadic parathyroid tumors
-
Tanaka C, Uchino S, Noguchi S, Nishioka T, Yamasaki H, Hashimoto K, et al. Biallelic inactivation by somatic mutations of the MEN1 gene in sporadic parathyroid tumors. Cancer Lett 2002, 175(2):175-179.
-
(2002)
Cancer Lett
, vol.175
, Issue.2
, pp. 175-179
-
-
Tanaka, C.1
Uchino, S.2
Noguchi, S.3
Nishioka, T.4
Yamasaki, H.5
Hashimoto, K.6
-
44
-
-
0032539632
-
Menin, the product of the MEN1 gene, is a nuclear protein
-
Guru SC, Goldsmith PK, Burns AL, Marx SJ, Spiegel AM, Collins FS, et al. Menin, the product of the MEN1 gene, is a nuclear protein. Proc Natl Acad Sci U S A 1998, 95(4):1630-1634.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, Issue.4
, pp. 1630-1634
-
-
Guru, S.C.1
Goldsmith, P.K.2
Burns, A.L.3
Marx, S.J.4
Spiegel, A.M.5
Collins, F.S.6
-
45
-
-
10344233731
-
Direct binding of DNA by tumor suppressor menin
-
La P, Silva AC, Hou Z, Wang H, Schnepp RW, Yan N, et al. Direct binding of DNA by tumor suppressor menin. J Biol Chem 2004, 279(47):49045-49054.
-
(2004)
J Biol Chem
, vol.279
, Issue.47
, pp. 49045-49054
-
-
La, P.1
Silva, A.C.2
Hou, Z.3
Wang, H.4
Schnepp, R.W.5
Yan, N.6
-
46
-
-
22444445436
-
Menin molecular interactions: insights into normal functions and tumorigenesis
-
Agarwal SK, Kennedy PA, Scacheri PC, Novotny EA, Hickman AB, Cerrato A, et al. Menin molecular interactions: insights into normal functions and tumorigenesis. Horm Metab Res 2005, 37(6):369-374.
-
(2005)
Horm Metab Res
, vol.37
, Issue.6
, pp. 369-374
-
-
Agarwal, S.K.1
Kennedy, P.A.2
Scacheri, P.C.3
Novotny, E.A.4
Hickman, A.B.5
Cerrato, A.6
-
47
-
-
0033534510
-
Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription
-
Agarwal SK, Guru SC, Heppner C, Erdos MR, Collins RM, Park SY, et al. Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription. Cell 1999, 96(1):143-152.
-
(1999)
Cell
, vol.96
, Issue.1
, pp. 143-152
-
-
Agarwal, S.K.1
Guru, S.C.2
Heppner, C.3
Erdos, M.R.4
Collins, R.M.5
Park, S.Y.6
-
48
-
-
0035957357
-
Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling
-
Kaji H, Canaff L, Lebrun JJ, Goltzman D, Hendy GN Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling. Proc Natl Acad Sci U S A 2001, 98(7):3837-3842.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, Issue.7
, pp. 3837-3842
-
-
Kaji, H.1
Canaff, L.2
Lebrun, J.J.3
Goltzman, D.4
Hendy, G.N.5
-
49
-
-
0037821661
-
Multiple tumor suppressor pathways negatively regulate telomerase
-
Lin SY, Elledge SJ Multiple tumor suppressor pathways negatively regulate telomerase. Cell 2003, 113(7):881-889.
-
(2003)
Cell
, vol.113
, Issue.7
, pp. 881-889
-
-
Lin, S.Y.1
Elledge, S.J.2
-
50
-
-
20044380143
-
Menin and MLL cooperatively regulate expression of cyclin-dependent kinase inhibitors
-
Milne TA, Hughes CM, Lloyd R, Yang Z, Rozenblatt-Rosen O, Dou Y, et al. Menin and MLL cooperatively regulate expression of cyclin-dependent kinase inhibitors. Proc Natl Acad Sci U S A 2005, 102(3):749-754.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, Issue.3
, pp. 749-754
-
-
Milne, T.A.1
Hughes, C.M.2
Lloyd, R.3
Yang, Z.4
Rozenblatt-Rosen, O.5
Dou, Y.6
-
51
-
-
0035970092
-
A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors
-
Crabtree JS, Scacheri PC, Ward JM, Garrett-Beal L, Emmert-Buck MR, Edgemon KA, et al. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors. Proc Natl Acad Sci U S A 2001, 98(3):1118-1123.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, Issue.3
, pp. 1118-1123
-
-
Crabtree, J.S.1
Scacheri, P.C.2
Ward, J.M.3
Garrett-Beal, L.4
Emmert-Buck, M.R.5
Edgemon, K.A.6
-
52
-
-
72549106938
-
Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia
-
Harding B, Lemos MC, Reed AA, Walls GV, Jeyabalan J, Bowl MR, et al. Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia. Endocr Relat Cancer 2009, 16(4):1313-1327.
-
(2009)
Endocr Relat Cancer
, vol.16
, Issue.4
, pp. 1313-1327
-
-
Harding, B.1
Lemos, M.C.2
Reed, A.A.3
Walls, G.V.4
Jeyabalan, J.5
Bowl, M.R.6
-
53
-
-
10744233863
-
Parathyroid gland-specific deletion of the mouse Men1 gene results in parathyroid neoplasia and hypercalcemic hyperparathyroidism
-
Libutti SK, Crabtree JS, Lorang D, Burns AL, Mazzanti C, Hewitt SM, et al. Parathyroid gland-specific deletion of the mouse Men1 gene results in parathyroid neoplasia and hypercalcemic hyperparathyroidism. Cancer Res 2003, 63(22):8022-8028.
-
(2003)
Cancer Res
, vol.63
, Issue.22
, pp. 8022-8028
-
-
Libutti, S.K.1
Crabtree, J.S.2
Lorang, D.3
Burns, A.L.4
Mazzanti, C.5
Hewitt, S.M.6
-
54
-
-
79953853401
-
Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas
-
Costa-Guda J, Marinoni I, Molatore S, Pellegata NS, Arnold A Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas. J Clin Endocrinol Metab 2011, 96(4):E701-E706.
-
(2011)
J Clin Endocrinol Metab
, vol.96
, Issue.4
-
-
Costa-Guda, J.1
Marinoni, I.2
Molatore, S.3
Pellegata, N.S.4
Arnold, A.5
-
55
-
-
0030040625
-
Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas
-
Tahara H, Smith AP, Gas RD, Cryns VL, Arnold A Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas. Cancer Res 1996, 56(3):599-605.
-
(1996)
Cancer Res
, vol.56
, Issue.3
, pp. 599-605
-
-
Tahara, H.1
Smith, A.P.2
Gas, R.D.3
Cryns, V.L.4
Arnold, A.5
-
56
-
-
0031784957
-
Novel chromosomal abnormalities identified by comparative genomic hybridization in parathyroid adenomas
-
Palanisamy N, Imanishi Y, Rao PH, Tahara H, Chaganti RS, Arnold A Novel chromosomal abnormalities identified by comparative genomic hybridization in parathyroid adenomas. J Clin Endocrinol Metab 1998, 83(5):1766-1770.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, Issue.5
, pp. 1766-1770
-
-
Palanisamy, N.1
Imanishi, Y.2
Rao, P.H.3
Tahara, H.4
Chaganti, R.S.5
Arnold, A.6
-
57
-
-
1542359453
-
Reduced p18INK4c, p21CIP1/WAF1 and p27KIP1 mRNA levels in tumours of primary and secondary hyperparathyroidism
-
Buchwald PC, Akerstrom G, Westin G Reduced p18INK4c, p21CIP1/WAF1 and p27KIP1 mRNA levels in tumours of primary and secondary hyperparathyroidism. Clin Endocrinol (Oxf) 2004, 60(3):389-393.
-
(2004)
Clin Endocrinol (Oxf)
, vol.60
, Issue.3
, pp. 389-393
-
-
Buchwald, P.C.1
Akerstrom, G.2
Westin, G.3
-
58
-
-
0031594658
-
Expression of p27kip1 and Ki-67 in benign and malignant thyroid tumors
-
Erickson LA, Jin L, Wollan PC, Thompson GB, van Heerden J, Lloyd RV Expression of p27kip1 and Ki-67 in benign and malignant thyroid tumors. Mod Pathol 1998, 11(2):169-174.
-
(1998)
Mod Pathol
, vol.11
, Issue.2
, pp. 169-174
-
-
Erickson, L.A.1
Jin, L.2
Wollan, P.C.3
Thompson, G.B.4
van Heerden, J.5
Lloyd, R.V.6
-
59
-
-
0036378184
-
Reduced p21, p27 and vitamin D receptor in the nodular hyperplasia in patients with advanced secondary hyperparathyroidism
-
Tokumoto M, Tsuruya K, Fukuda K, Kanai H, Kuroki S, Hirakata H Reduced p21, p27 and vitamin D receptor in the nodular hyperplasia in patients with advanced secondary hyperparathyroidism. Kidney Int 2002, 62(4):1196-1207.
-
(2002)
Kidney Int
, vol.62
, Issue.4
, pp. 1196-1207
-
-
Tokumoto, M.1
Tsuruya, K.2
Fukuda, K.3
Kanai, H.4
Kuroki, S.5
Hirakata, H.6
-
60
-
-
0042532260
-
Understanding p27(kip1) deregulation in cancer: down-regulation or mislocalization
-
Viglietto G, Motti ML, Fusco A Understanding p27(kip1) deregulation in cancer: down-regulation or mislocalization. Cell Cycle 2002, 1(6):394-400.
-
(2002)
Cell Cycle
, vol.1
, Issue.6
, pp. 394-400
-
-
Viglietto, G.1
Motti, M.L.2
Fusco, A.3
-
61
-
-
32044441426
-
How to decrease p27Kip1 levels during tumor development
-
Koff A How to decrease p27Kip1 levels during tumor development. Cancer Cell 2006, 9(2):75-76.
-
(2006)
Cancer Cell
, vol.9
, Issue.2
, pp. 75-76
-
-
Koff, A.1
-
62
-
-
15844415946
-
Enhanced growth of mice lacking the cyclin-dependent kinase inhibitor function of p27(Kip1)
-
Kiyokawa H, Kineman RD, Manova-Todorova KO, Soares VC, Hoffman ES, Ono M, et al. Enhanced growth of mice lacking the cyclin-dependent kinase inhibitor function of p27(Kip1). Cell 1996, 85(5):721-732.
-
(1996)
Cell
, vol.85
, Issue.5
, pp. 721-732
-
-
Kiyokawa, H.1
Kineman, R.D.2
Manova-Todorova, K.O.3
Soares, V.C.4
Hoffman, E.S.5
Ono, M.6
-
63
-
-
15844384256
-
A syndrome of multiorgan hyperplasia with features of gigantism, tumorigenesis, and female sterility in p27(Kip1)-deficient mice
-
Fero ML, Rivkin M, Tasch M, Porter P, Carow CE, Firpo E, et al. A syndrome of multiorgan hyperplasia with features of gigantism, tumorigenesis, and female sterility in p27(Kip1)-deficient mice. Cell 1996, 85(5):733-744.
-
(1996)
Cell
, vol.85
, Issue.5
, pp. 733-744
-
-
Fero, M.L.1
Rivkin, M.2
Tasch, M.3
Porter, P.4
Carow, C.E.5
Firpo, E.6
-
64
-
-
0030010591
-
Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumors
-
Nakayama K, Ishida N, Shirane M, Inomata A, Inoue T, Shishido N, et al. Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumors. Cell 1996, 85(5):707-720.
-
(1996)
Cell
, vol.85
, Issue.5
, pp. 707-720
-
-
Nakayama, K.1
Ishida, N.2
Shirane, M.3
Inomata, A.4
Inoue, T.5
Shishido, N.6
-
65
-
-
0033864297
-
Functional collaboration between different cyclin-dependent kinase inhibitors suppresses tumor growth with distinct tissue specificity
-
Franklin DS, Godfrey VL, O'Brien DA, Deng C, Xiong Y Functional collaboration between different cyclin-dependent kinase inhibitors suppresses tumor growth with distinct tissue specificity. Mol Cell Biol 2000, 20(16):6147-6158.
-
(2000)
Mol Cell Biol
, vol.20
, Issue.16
, pp. 6147-6158
-
-
Franklin, D.S.1
Godfrey, V.L.2
O'Brien, D.A.3
Deng, C.4
Xiong, Y.5
-
66
-
-
33846907737
-
P18Ink4c, but not p27Kip1, collaborates with Men1 to suppress neuroendocrine organ tumors
-
Bai F, Pei XH, Nishikawa T, Smith MD, Xiong Y p18Ink4c, but not p27Kip1, collaborates with Men1 to suppress neuroendocrine organ tumors. Mol Cell Biol 2007, 27(4):1495-1504.
-
(2007)
Mol Cell Biol
, vol.27
, Issue.4
, pp. 1495-1504
-
-
Bai, F.1
Pei, X.H.2
Nishikawa, T.3
Smith, M.D.4
Xiong, Y.5
-
67
-
-
0142213734
-
Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma
-
Shattuck TM, Valimaki S, Obara T, Gaz RD, Clark OH, Shoback D, et al. Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. N Engl J Med 2003, 349(18):1722-1729.
-
(2003)
N Engl J Med
, vol.349
, Issue.18
, pp. 1722-1729
-
-
Shattuck, T.M.1
Valimaki, S.2
Obara, T.3
Gaz, R.D.4
Clark, O.H.5
Shoback, D.6
-
68
-
-
24344498667
-
HRPT2 mutational analysis of typical sporadic parathyroid adenomas
-
Krebs LJ, Shattuck TM, Arnold A HRPT2 mutational analysis of typical sporadic parathyroid adenomas. J Clin Endocrinol Metab 2005, 90(9):5015-5017.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, Issue.9
, pp. 5015-5017
-
-
Krebs, L.J.1
Shattuck, T.M.2
Arnold, A.3
-
69
-
-
0041328511
-
HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours
-
Howell VM, Haven CJ, Kahnoski K, Khoo SK, Petillo D, Chen J, et al. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J Med Genet 2003, 40(9):657-663.
-
(2003)
J Med Genet
, vol.40
, Issue.9
, pp. 657-663
-
-
Howell, V.M.1
Haven, C.J.2
Kahnoski, K.3
Khoo, S.K.4
Petillo, D.5
Chen, J.6
-
70
-
-
8744299920
-
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors
-
Cetani F, Pardi E, Borsari S, Viacava P, Dipollina G, Cianferotti L, et al. Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors. J Clin Endocrinol Metab 2004, 89(11):5583-5591.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, Issue.11
, pp. 5583-5591
-
-
Cetani, F.1
Pardi, E.2
Borsari, S.3
Viacava, P.4
Dipollina, G.5
Cianferotti, L.6
-
71
-
-
33747668789
-
Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance
-
Guarnieri V, Scillitani A, Muscarella LA, Battista C, Bonfitto N, Bisceglia M, et al. Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance. J Clin Endocrinol Metab 2006, 91(8):2827-2832.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, Issue.8
, pp. 2827-2832
-
-
Guarnieri, V.1
Scillitani, A.2
Muscarella, L.A.3
Battista, C.4
Bonfitto, N.5
Bisceglia, M.6
-
73
-
-
33646555522
-
Parafibromin/Hyrax activates Wnt/Wg target gene transcription by direct association with beta-catenin/Armadillo
-
Mosimann C, Hausmann G, Basler K Parafibromin/Hyrax activates Wnt/Wg target gene transcription by direct association with beta-catenin/Armadillo. Cell 2006, 125(2):327-341.
-
(2006)
Cell
, vol.125
, Issue.2
, pp. 327-341
-
-
Mosimann, C.1
Hausmann, G.2
Basler, K.3
-
74
-
-
0033545845
-
The cyclin D1 gene is a target of the beta-catenin/LEF-1 pathway
-
Shtutman M, Zhurinsky J, Simcha I, Albanese C, D'Amico M, Pestell R, et al. The cyclin D1 gene is a target of the beta-catenin/LEF-1 pathway. Proc Natl Acad Sci U S A 1999, 96(10):5522-5527.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, Issue.10
, pp. 5522-5527
-
-
Shtutman, M.1
Zhurinsky, J.2
Simcha, I.3
Albanese, C.4
D'Amico, M.5
Pestell, R.6
-
75
-
-
0033119801
-
Beta-catenin regulates expression of cyclin D1 in colon carcinoma cells
-
Tetsu O, McCormick F Beta-catenin regulates expression of cyclin D1 in colon carcinoma cells. Nature 1999, 398(6726):422-426.
-
(1999)
Nature
, vol.398
, Issue.6726
, pp. 422-426
-
-
Tetsu, O.1
McCormick, F.2
-
76
-
-
1942537708
-
The significance of the Wnt pathway in the pathology of human cancers
-
Karim R, Tse G, Putti T, Scolyer R, Lee S The significance of the Wnt pathway in the pathology of human cancers. Pathology 2004, 36(2):120-128.
-
(2004)
Pathology
, vol.36
, Issue.2
, pp. 120-128
-
-
Karim, R.1
Tse, G.2
Putti, T.3
Scolyer, R.4
Lee, S.5
-
77
-
-
42349096478
-
Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult mice
-
Wang P, Bowl MR, Bender S, Peng J, Farber L, Chen J, et al. Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult mice. Mol Cell Biol 2008, 28(9):2930-2940.
-
(2008)
Mol Cell Biol
, vol.28
, Issue.9
, pp. 2930-2940
-
-
Wang, P.1
Bowl, M.R.2
Bender, S.3
Peng, J.4
Farber, L.5
Chen, J.6
-
78
-
-
33746808398
-
Wnt/beta-catenin signaling in development and disease
-
Clevers H Wnt/beta-catenin signaling in development and disease. Cell 2006, 127(3):469-480.
-
(2006)
Cell
, vol.127
, Issue.3
, pp. 469-480
-
-
Clevers, H.1
-
79
-
-
0030949463
-
Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC
-
Morin PJ, Sparks AB, Korinek V, Barker N, Clevers H, Vogelstein B, et al. Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC. Science 1997, 275(5307):1787-1790.
-
(1997)
Science
, vol.275
, Issue.5307
, pp. 1787-1790
-
-
Morin, P.J.1
Sparks, A.B.2
Korinek, V.3
Barker, N.4
Clevers, H.5
Vogelstein, B.6
-
80
-
-
13644269949
-
Wnt signalling and the mechanistic basis of tumour development
-
Ilyas M Wnt signalling and the mechanistic basis of tumour development. J Pathol 2005, 205(2):130-144.
-
(2005)
J Pathol
, vol.205
, Issue.2
, pp. 130-144
-
-
Ilyas, M.1
-
81
-
-
33751524195
-
Accumulation of non-phosphorylated {beta}-catenin and c-myc in primary and uremic secondary hyperparathyroid tumors
-
Bjorklund P, Akerstrom G, Westin G Accumulation of non-phosphorylated {beta}-catenin and c-myc in primary and uremic secondary hyperparathyroid tumors. J Clin Endocrinol Metab 2006.
-
(2006)
J Clin Endocrinol Metab
-
-
Bjorklund, P.1
Akerstrom, G.2
Westin, G.3
-
82
-
-
46349098659
-
Stabilizing mutation of CTNNB1/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients
-
Bjorklund P, Lindberg D, Akerstrom G, Westin G Stabilizing mutation of CTNNB1/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients. Mol Cancer 2008, 7:53.
-
(2008)
Mol Cancer
, vol.7
, pp. 53
-
-
Bjorklund, P.1
Lindberg, D.2
Akerstrom, G.3
Westin, G.4
-
83
-
-
0033753426
-
Nuclear accumulation of b-catenin in human endocrine tumors: association with Ki-67 (MIB-1) proliferative activity
-
Semba S, Kusumi R, Moriya T, Sasano H Nuclear accumulation of b-catenin in human endocrine tumors: association with Ki-67 (MIB-1) proliferative activity. Endocr Pathol 2000, 11(3):243-250.
-
(2000)
Endocr Pathol
, vol.11
, Issue.3
, pp. 243-250
-
-
Semba, S.1
Kusumi, R.2
Moriya, T.3
Sasano, H.4
-
84
-
-
34147126074
-
Absence of stabilizing mutations of beta-catenin encoded by CTNNB1 exon 3 in a large series of sporadic parathyroid adenomas
-
Costa-Guda J, Arnold A Absence of stabilizing mutations of beta-catenin encoded by CTNNB1 exon 3 in a large series of sporadic parathyroid adenomas. J Clin Endocrinol Metab 2007, 92(4):1564-1566.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, Issue.4
, pp. 1564-1566
-
-
Costa-Guda, J.1
Arnold, A.2
-
85
-
-
64549160727
-
Loss of expression for the Wnt pathway components adenomatous polyposis coli and glycogen synthase kinase 3-beta in parathyroid carcinomas
-
Juhlin CC, Haglund F, Villablanca A, Forsberg L, Sandelin K, Branstrom R, et al. Loss of expression for the Wnt pathway components adenomatous polyposis coli and glycogen synthase kinase 3-beta in parathyroid carcinomas. Int J Oncol 2009, 34(2):481-492.
-
(2009)
Int J Oncol
, vol.34
, Issue.2
, pp. 481-492
-
-
Juhlin, C.C.1
Haglund, F.2
Villablanca, A.3
Forsberg, L.4
Sandelin, K.5
Branstrom, R.6
-
86
-
-
77449145777
-
Beta-catenin activation is not involved in sporadic parathyroid carcinomas and adenomas
-
Cetani F, Pardi E, Banti C, Collecchi P, Viacava P, Borsari S, et al. Beta-catenin activation is not involved in sporadic parathyroid carcinomas and adenomas. Endocr Relat Cancer 2010, 17(1):1-6.
-
(2010)
Endocr Relat Cancer
, vol.17
, Issue.1
, pp. 1-6
-
-
Cetani, F.1
Pardi, E.2
Banti, C.3
Collecchi, P.4
Viacava, P.5
Borsari, S.6
-
87
-
-
77957041830
-
Lack of S37A CTNNB1/beta-catenin mutations in a Swedish cohort of 98 parathyroid adenomas
-
Haglund F, Andreasson A, Nilsson IL, Hoog A, Larsson C, Juhlin CC Lack of S37A CTNNB1/beta-catenin mutations in a Swedish cohort of 98 parathyroid adenomas. Clin Endocrinol (Oxf) 2010, 73(4):552-553.
-
(2010)
Clin Endocrinol (Oxf)
, vol.73
, Issue.4
, pp. 552-553
-
-
Haglund, F.1
Andreasson, A.2
Nilsson, I.L.3
Hoog, A.4
Larsson, C.5
Juhlin, C.C.6
-
88
-
-
0036511411
-
Immunohistochemistry of cyclin D1 and beta-catenin, and mutational analysis of exon 3 of beta-catenin gene in parathyroid adenomas
-
Ikeda S, Ishizaki Y, Shimizu Y, Fujimori M, Ojima Y, Okajima M, et al. Immunohistochemistry of cyclin D1 and beta-catenin, and mutational analysis of exon 3 of beta-catenin gene in parathyroid adenomas. Int J Oncol 2002, 20(3):463-466.
-
(2002)
Int J Oncol
, vol.20
, Issue.3
, pp. 463-466
-
-
Ikeda, S.1
Ishizaki, Y.2
Shimizu, Y.3
Fujimori, M.4
Ojima, Y.5
Okajima, M.6
-
89
-
-
0001835323
-
Molecular basis of primary hyperparathyroidism
-
Academic Press, San Diego, J.P. Bilezikian (Ed.)
-
Arnold A Molecular basis of primary hyperparathyroidism. The Parathyroids. 2001, 331-347. Academic Press, San Diego. 2nd ed. J.P. Bilezikian (Ed.).
-
(2001)
The Parathyroids.
, pp. 331-347
-
-
Arnold, A.1
-
90
-
-
0025806904
-
A novel cyclin encoded by a bcl1-linked candidate oncogene
-
Motokura T, Bloom T, Kim HG, Juppner H, Ruderman JV, Kronenberg HM, et al. A novel cyclin encoded by a bcl1-linked candidate oncogene. Nature 1991, 350(6318):512-515.
-
(1991)
Nature
, vol.350
, Issue.6318
, pp. 512-515
-
-
Motokura, T.1
Bloom, T.2
Kim, H.G.3
Juppner, H.4
Ruderman, J.V.5
Kronenberg, H.M.6
-
91
-
-
70350029364
-
Molecular genetics of parathyroid disease
-
Westin G, Bjorklund P, Akerstrom G Molecular genetics of parathyroid disease. World J Surg 2009, 33(11):2224-2233.
-
(2009)
World J Surg
, vol.33
, Issue.11
, pp. 2224-2233
-
-
Westin, G.1
Bjorklund, P.2
Akerstrom, G.3
-
92
-
-
0029940779
-
Cyclin D1/PRAD1 expression in parathyroid adenomas: an immunohistochemical study
-
Hsi ED, Zukerberg LR, Yang WI, Arnold A Cyclin D1/PRAD1 expression in parathyroid adenomas: an immunohistochemical study. J Clin Endocrinol Metab 1996, 81(5):1736-1739.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, Issue.5
, pp. 1736-1739
-
-
Hsi, E.D.1
Zukerberg, L.R.2
Yang, W.I.3
Arnold, A.4
-
93
-
-
0032938805
-
Expression of cyclin D1 in parathyroid carcinomas, adenomas, and hyperplasias: a paraffin immunohistochemical study
-
Vasef MA, Brynes RK, Sturm M, Bromley C, Robinson RA Expression of cyclin D1 in parathyroid carcinomas, adenomas, and hyperplasias: a paraffin immunohistochemical study. Mod Pathol 1999, 12(4):412-416.
-
(1999)
Mod Pathol
, vol.12
, Issue.4
, pp. 412-416
-
-
Vasef, M.A.1
Brynes, R.K.2
Sturm, M.3
Bromley, C.4
Robinson, R.A.5
-
94
-
-
0032954756
-
Expression of PRAD1/cyclin D1, retinoblastoma gene products, and Ki67 in parathyroid hyperplasia caused by chronic renal failure versus primary adenoma
-
Tominaga Y, Tsuzuki T, Uchida K, Haba T, Otsuka S, Ichimori T, et al. Expression of PRAD1/cyclin D1, retinoblastoma gene products, and Ki67 in parathyroid hyperplasia caused by chronic renal failure versus primary adenoma. Kidney Int 1999, 55(4):1375-1383.
-
(1999)
Kidney Int
, vol.55
, Issue.4
, pp. 1375-1383
-
-
Tominaga, Y.1
Tsuzuki, T.2
Uchida, K.3
Haba, T.4
Otsuka, S.5
Ichimori, T.6
-
95
-
-
0029443097
-
The cyclin D1/PRAD1 oncogene in human neoplasia
-
Arnold A The cyclin D1/PRAD1 oncogene in human neoplasia. J Investig Med 1995, 43(6):543-549.
-
(1995)
J Investig Med
, vol.43
, Issue.6
, pp. 543-549
-
-
Arnold, A.1
-
96
-
-
23044508946
-
Cyclin D1 in breast cancer pathogenesis
-
Arnold A, Papanikolaou A Cyclin D1 in breast cancer pathogenesis. J Clin Oncol 2005, 23(18):4215-4224.
-
(2005)
J Clin Oncol
, vol.23
, Issue.18
, pp. 4215-4224
-
-
Arnold, A.1
Papanikolaou, A.2
-
97
-
-
0035014450
-
Primary hyperparathyroidism caused by parathyroid-targeted overexpression of cyclin D1 in transgenic mice
-
Imanishi Y, Hosokawa Y, Yoshimoto K, Schipani E, Mallya S, Papanikolaou A, et al. Primary hyperparathyroidism caused by parathyroid-targeted overexpression of cyclin D1 in transgenic mice. J Clin Invest 2001, 107(9):1093-1102.
-
(2001)
J Clin Invest
, vol.107
, Issue.9
, pp. 1093-1102
-
-
Imanishi, Y.1
Hosokawa, Y.2
Yoshimoto, K.3
Schipani, E.4
Mallya, S.5
Papanikolaou, A.6
-
98
-
-
36849054642
-
Mitochondrial DNA mutations in oxyphilic and chief cell parathyroid adenomas
-
Costa-Guda J, Tokura T, Roth SI, Arnold A Mitochondrial DNA mutations in oxyphilic and chief cell parathyroid adenomas. BMC Endocr Disord 2007, 7:8.
-
(2007)
BMC Endocr Disord
, vol.7
, pp. 8
-
-
Costa-Guda, J.1
Tokura, T.2
Roth, S.I.3
Arnold, A.4
-
99
-
-
0007099343
-
The cytology of the normal parathyroid glands of man and Virginia deer; a light and electron microscopic study with morphologic evidence of secretory activity
-
Munger BL, Roth SI The cytology of the normal parathyroid glands of man and Virginia deer; a light and electron microscopic study with morphologic evidence of secretory activity. J Cell Biol 1963, 16:379-400.
-
(1963)
J Cell Biol
, vol.16
, pp. 379-400
-
-
Munger, B.L.1
Roth, S.I.2
-
100
-
-
0029995894
-
Role of the RET proto-oncogene in sporadic hyperparathyroidism and in hyperparathyroidism of multiple endocrine neoplasia type 2
-
Pausova Z, Soliman E, Amizuka N, Janicic N, Konrad EM, Arnold A, et al. Role of the RET proto-oncogene in sporadic hyperparathyroidism and in hyperparathyroidism of multiple endocrine neoplasia type 2. J Clin Endocrinol Metab 1996, 81(7):2711-2718.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, Issue.7
, pp. 2711-2718
-
-
Pausova, Z.1
Soliman, E.2
Amizuka, N.3
Janicic, N.4
Konrad, E.M.5
Arnold, A.6
-
101
-
-
10144256536
-
A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor
-
Pearce SH, Williamson C, Kifor O, Bai M, Coulthard MG, Davies M, et al. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor. N Engl J Med 1996, 335(15):1115-1122.
-
(1996)
N Engl J Med
, vol.335
, Issue.15
, pp. 1115-1122
-
-
Pearce, S.H.1
Williamson, C.2
Kifor, O.3
Bai, M.4
Coulthard, M.G.5
Davies, M.6
-
102
-
-
0027787680
-
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
-
Pollak MR, Brown EM, Chou YH, Hebert SC, Marx SJ, Steinmann B, et al. Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Cell 1993, 75(7):1297-1303.
-
(1993)
Cell
, vol.75
, Issue.7
, pp. 1297-1303
-
-
Pollak, M.R.1
Brown, E.M.2
Chou, Y.H.3
Hebert, S.C.4
Marx, S.J.5
Steinmann, B.6
-
103
-
-
0032982710
-
No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas
-
Cetani F, Pinchera A, Pardi E, Cianferotti L, Vignali E, Picone A, et al. No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas. J Bone Miner Res 1999, 14(6):878-882.
-
(1999)
J Bone Miner Res
, vol.14
, Issue.6
, pp. 878-882
-
-
Cetani, F.1
Pinchera, A.2
Pardi, E.3
Cianferotti, L.4
Vignali, E.5
Picone, A.6
-
104
-
-
0028826364
-
Mutational analysis of the extracellular Ca(2+)-sensing receptor gene in human parathyroid tumors
-
Hosokawa Y, Pollak MR, Brown EM, Arnold A Mutational analysis of the extracellular Ca(2+)-sensing receptor gene in human parathyroid tumors. J Clin Endocrinol Metab 1995, 80(11):3107-3110.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, Issue.11
, pp. 3107-3110
-
-
Hosokawa, Y.1
Pollak, M.R.2
Brown, E.M.3
Arnold, A.4
-
105
-
-
0032764057
-
The effects of vitamin D insufficiency in patients with primary hyperparathyroidism
-
Silverberg SJ, Shane E, Dempster DW, Bilezikian JP The effects of vitamin D insufficiency in patients with primary hyperparathyroidism. Am J Med 1999, 107(6):561-567.
-
(1999)
Am J Med
, vol.107
, Issue.6
, pp. 561-567
-
-
Silverberg, S.J.1
Shane, E.2
Dempster, D.W.3
Bilezikian, J.P.4
-
106
-
-
0026693809
-
Sequences in the human parathyroid hormone gene that bind the 1,25-dihydroxyvitamin D3 receptor and mediate transcriptional repression in response to 1,25-dihydroxyvitamin D3
-
Demay MB, Kiernan MS, DeLuca HF, Kronenberg HM Sequences in the human parathyroid hormone gene that bind the 1,25-dihydroxyvitamin D3 receptor and mediate transcriptional repression in response to 1,25-dihydroxyvitamin D3. Proc Natl Acad Sci U S A 1992, 89(17):8097-8101.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, Issue.17
, pp. 8097-8101
-
-
Demay, M.B.1
Kiernan, M.S.2
DeLuca, H.F.3
Kronenberg, H.M.4
-
107
-
-
0033397335
-
Regulation of the parathyroid hormone gene by vitamin D, calcium and phosphate
-
Silver J, Yalcindag C, Sela-Brown A, Kilav R, Naveh-Many T Regulation of the parathyroid hormone gene by vitamin D, calcium and phosphate. Kidney Int Suppl 1999, 73:S2-S7.
-
(1999)
Kidney Int Suppl
, vol.73
-
-
Silver, J.1
Yalcindag, C.2
Sela-Brown, A.3
Kilav, R.4
Naveh-Many, T.5
-
108
-
-
0023676102
-
1,25(OH)2D3 inhibits hormone secretion and proliferation but not functional dedifferentiation of cultured bovine parathyroid cells
-
Nygren P, Larsson R, Johansson H, Ljunghall S, Rastad J, Akerstrom G 1,25(OH)2D3 inhibits hormone secretion and proliferation but not functional dedifferentiation of cultured bovine parathyroid cells. Calcif Tissue Int 1988, 43(4):213-218.
-
(1988)
Calcif Tissue Int
, vol.43
, Issue.4
, pp. 213-218
-
-
Nygren, P.1
Larsson, R.2
Johansson, H.3
Ljunghall, S.4
Rastad, J.5
Akerstrom, G.6
-
109
-
-
0022350156
-
1,25-Dihydroxyvitamin D3 suppresses parathyroid hormone secretion from bovine parathyroid cells in tissue culture
-
Cantley LK, Russell J, Lettieri D, Sherwood LM 1,25-Dihydroxyvitamin D3 suppresses parathyroid hormone secretion from bovine parathyroid cells in tissue culture. Endocrinology 1985, 117(5):2114-2119.
-
(1985)
Endocrinology
, vol.117
, Issue.5
, pp. 2114-2119
-
-
Cantley, L.K.1
Russell, J.2
Lettieri, D.3
Sherwood, L.M.4
-
110
-
-
23044453030
-
Vitamin D in normal and pathological parathyroid glands: new prospects for treating hyperparathyroidism (review)
-
Buchwald PC, Westin G, Akerstrom G Vitamin D in normal and pathological parathyroid glands: new prospects for treating hyperparathyroidism (review). Int J Mol Med 2005, 15(4):701-706.
-
(2005)
Int J Mol Med
, vol.15
, Issue.4
, pp. 701-706
-
-
Buchwald, P.C.1
Westin, G.2
Akerstrom, G.3
-
111
-
-
0031786539
-
Vitamin D receptor (VDR) and parathyroid hormone messenger ribonucleic acid levels correspond to polymorphic VDR alleles in human parathyroid tumors
-
Carling T, Rastad J, Akerstrom G, Westin G Vitamin D receptor (VDR) and parathyroid hormone messenger ribonucleic acid levels correspond to polymorphic VDR alleles in human parathyroid tumors. J Clin Endocrinol Metab 1998, 83(7):2255-2259.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, Issue.7
, pp. 2255-2259
-
-
Carling, T.1
Rastad, J.2
Akerstrom, G.3
Westin, G.4
-
112
-
-
0034455926
-
Reduced parathyroid vitamin D receptor messenger ribonucleic acid levels in primary and secondary hyperparathyroidism
-
Carling T, Rastad J, Szabo E, Westin G, Akerstrom G Reduced parathyroid vitamin D receptor messenger ribonucleic acid levels in primary and secondary hyperparathyroidism. J Clin Endocrinol Metab 2000, 85(5):2000-2003.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, Issue.5
, pp. 2000-2003
-
-
Carling, T.1
Rastad, J.2
Szabo, E.3
Westin, G.4
Akerstrom, G.5
-
113
-
-
33845492429
-
Mutational analysis of the vitamin D receptor does not support its candidacy as a tumor suppressor gene in parathyroid adenomas
-
Samander EH, Arnold A Mutational analysis of the vitamin D receptor does not support its candidacy as a tumor suppressor gene in parathyroid adenomas. J Clin Endocrinol Metab 2006, 91(12):5019-5021.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, Issue.12
, pp. 5019-5021
-
-
Samander, E.H.1
Arnold, A.2
-
114
-
-
17744385121
-
Vitamin D receptor as a candidate tumor- suppressor gene in severe hyperparathyroidism of uremia
-
Brown SB, Brierley TT, Palanisamy N, Salusky IB, Goodman W, Brandi ML, et al. Vitamin D receptor as a candidate tumor- suppressor gene in severe hyperparathyroidism of uremia. J Clin Endocrinol Metab 2000, 85(2):868-872.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, Issue.2
, pp. 868-872
-
-
Brown, S.B.1
Brierley, T.T.2
Palanisamy, N.3
Salusky, I.B.4
Goodman, W.5
Brandi, M.L.6
-
115
-
-
0026457022
-
Ras mutations in endocrine tumors: mutation detection by polymerase chain reaction-single strand conformation polymorphism
-
Yoshimoto K, Iwahana H, Fukuda A, Sano T, Katsuragi K, Kinoshita M, et al. ras mutations in endocrine tumors: mutation detection by polymerase chain reaction-single strand conformation polymorphism. Jpn J Cancer Res 1992, 83(10):1057-1062.
-
(1992)
Jpn J Cancer Res
, vol.83
, Issue.10
, pp. 1057-1062
-
-
Yoshimoto, K.1
Iwahana, H.2
Fukuda, A.3
Sano, T.4
Katsuragi, K.5
Kinoshita, M.6
-
116
-
-
0028179429
-
P53 abnormalities in human parathyroid carcinoma
-
Cryns VL, Rubio MP, Thor AD, Louis DN, Arnold A p53 abnormalities in human parathyroid carcinoma. J Clin Endocrinol Metab 1994, 78(6):1320-1324.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, Issue.6
, pp. 1320-1324
-
-
Cryns, V.L.1
Rubio, M.P.2
Thor, A.D.3
Louis, D.N.4
Arnold, A.5
-
117
-
-
0024514647
-
Allelotype of colorectal carcinomas
-
Vogelstein B, Fearon ER, Kern SE, Hamilton SR, Preisinger AC, Nakamura Y, et al. Allelotype of colorectal carcinomas. Science 1989, 244(4901):207-211.
-
(1989)
Science
, vol.244
, Issue.4901
, pp. 207-211
-
-
Vogelstein, B.1
Fearon, E.R.2
Kern, S.E.3
Hamilton, S.R.4
Preisinger, A.C.5
Nakamura, Y.6
-
118
-
-
0020042005
-
Parathyroid carcinoma: a clinical study of seven cases of functioning and two cases of nonfunctioning parathyroid cancer
-
Aldinger KA, Hickey RC, Ibanez ML, Samaan NA Parathyroid carcinoma: a clinical study of seven cases of functioning and two cases of nonfunctioning parathyroid cancer. Cancer 1982, 49(2):388-397.
-
(1982)
Cancer
, vol.49
, Issue.2
, pp. 388-397
-
-
Aldinger, K.A.1
Hickey, R.C.2
Ibanez, M.L.3
Samaan, N.A.4
-
119
-
-
0019985803
-
Parathyroid carcinoma, adenoma and hyperplasia in a case of chronic renal insufficiency on dialysis
-
Berland Y, Olmer M, Lebreuil G, Grisoli J Parathyroid carcinoma, adenoma and hyperplasia in a case of chronic renal insufficiency on dialysis. Clin Nephrol 1982, 18(3):154-158.
-
(1982)
Clin Nephrol
, vol.18
, Issue.3
, pp. 154-158
-
-
Berland, Y.1
Olmer, M.2
Lebreuil, G.3
Grisoli, J.4
-
120
-
-
0021265528
-
Parathyroid hyperplasia and carcinoma within one gland
-
Desch CE, Arsensis G, Woolf PD, May AG, Amatruda JM Parathyroid hyperplasia and carcinoma within one gland. Am J Med 1984, 77(1):131-134.
-
(1984)
Am J Med
, vol.77
, Issue.1
, pp. 131-134
-
-
Desch, C.E.1
Arsensis, G.2
Woolf, P.D.3
May, A.G.4
Amatruda, J.M.5
-
121
-
-
0020579080
-
Concurrent primary parathyroid hyperplasia and parathyroid carcinoma
-
Haghighi P, Astarita RW, Wepsic HT, Wolf PL Concurrent primary parathyroid hyperplasia and parathyroid carcinoma. Arch Pathol Lab Med 1983, 107(7):349-350.
-
(1983)
Arch Pathol Lab Med
, vol.107
, Issue.7
, pp. 349-350
-
-
Haghighi, P.1
Astarita, R.W.2
Wepsic, H.T.3
Wolf, P.L.4
-
122
-
-
0017716432
-
A case of parathyroid carcinoma concurred with hyperplasia: an electron microscopic study
-
Murayama T, Kawabe K, Tagami M A case of parathyroid carcinoma concurred with hyperplasia: an electron microscopic study. J Urol 1977, 118(1 Pt 1):126-127.
-
(1977)
J Urol
, vol.118
, Issue.1 PART 1
, pp. 126-127
-
-
Murayama, T.1
Kawabe, K.2
Tagami, M.3
-
123
-
-
0033304944
-
Alternative genetic pathways in parathyroid tumorigenesis
-
Farnebo F, Kytola S, Teh BT, Dwight T, Wong FK, Hoog A, et al. Alternative genetic pathways in parathyroid tumorigenesis. J Clin Endocrinol Metab 1999, 84(10):3775-3780.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, Issue.10
, pp. 3775-3780
-
-
Farnebo, F.1
Kytola, S.2
Teh, B.T.3
Dwight, T.4
Wong, F.K.5
Hoog, A.6
-
124
-
-
0033902799
-
Patterns of chromosomal imbalances in parathyroid carcinomas
-
Kytola S, Farnebo F, Obara T, Isola J, Grimelius L, Farnebo LO, et al. Patterns of chromosomal imbalances in parathyroid carcinomas. Am J Pathol 2000, 157(2):579-586.
-
(2000)
Am J Pathol
, vol.157
, Issue.2
, pp. 579-586
-
-
Kytola, S.1
Farnebo, F.2
Obara, T.3
Isola, J.4
Grimelius, L.5
Farnebo, L.O.6
-
125
-
-
0032191661
-
Comparative genomic hybridization analysis of human parathyroid tumors
-
Agarwal SK, Schrock E, Kester MB, Burns AL, Heffess CS, Ried T, et al. Comparative genomic hybridization analysis of human parathyroid tumors. Cancer Genet Cytogenet 1998, 106(1):30-36.
-
(1998)
Cancer Genet Cytogenet
, vol.106
, Issue.1
, pp. 30-36
-
-
Agarwal, S.K.1
Schrock, E.2
Kester, M.B.3
Burns, A.L.4
Heffess, C.S.5
Ried, T.6
-
126
-
-
0024543856
-
Ectopic production of parathyroid hormone by small cell lung cancer in a patient with hypercalcemia
-
Yoshimoto K, Yamasaki R, Sakai H, Tezuka U, Takahashi M, Iizuka M, et al. Ectopic production of parathyroid hormone by small cell lung cancer in a patient with hypercalcemia. J Clin Endocrinol Metab 1989, 68(5):976-981.
-
(1989)
J Clin Endocrinol Metab
, vol.68
, Issue.5
, pp. 976-981
-
-
Yoshimoto, K.1
Yamasaki, R.2
Sakai, H.3
Tezuka, U.4
Takahashi, M.5
Iizuka, M.6
-
127
-
-
0027309131
-
Production of parathyroid hormone by a malignant nonparathyroid tumor in a hypercalcemic patient
-
Strewler GJ, Budayr AA, Clark OH, Nissenson RA Production of parathyroid hormone by a malignant nonparathyroid tumor in a hypercalcemic patient. J Clin Endocrinol Metab 1993, 76(5):1373-1375.
-
(1993)
J Clin Endocrinol Metab
, vol.76
, Issue.5
, pp. 1373-1375
-
-
Strewler, G.J.1
Budayr, A.A.2
Clark, O.H.3
Nissenson, R.A.4
-
128
-
-
0027965648
-
A thymoma as a cause of true ectopic hyperparathyroidism
-
Rizzoli R, Pache JC, Didierjean L, Burger A, Bonjour JP A thymoma as a cause of true ectopic hyperparathyroidism. J Clin Endocrinol Metab 1994, 79(3):912-915.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, Issue.3
, pp. 912-915
-
-
Rizzoli, R.1
Pache, J.C.2
Didierjean, L.3
Burger, A.4
Bonjour, J.P.5
-
129
-
-
0025036356
-
Hypercalcemia and ectopic secretion of parathyroid hormone by an ovarian carcinoma with rearrangement of the gene for parathyroid hormone
-
Nussbaum SR, Gaz RD, Arnold A Hypercalcemia and ectopic secretion of parathyroid hormone by an ovarian carcinoma with rearrangement of the gene for parathyroid hormone. N Engl J Med 1990, 323(19):1324-1328.
-
(1990)
N Engl J Med
, vol.323
, Issue.19
, pp. 1324-1328
-
-
Nussbaum, S.R.1
Gaz, R.D.2
Arnold, A.3
-
130
-
-
32544450117
-
Hypercalcemia of malignancy due to ectopic transactivation of the parathyroid hormone gene
-
VanHouten JN, Yu N, Rimm D, Dotto J, Arnold A, Wysolmerski JJ, et al. Hypercalcemia of malignancy due to ectopic transactivation of the parathyroid hormone gene. J Clin Endocrinol Metab 2006, 91(2):580-583.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, Issue.2
, pp. 580-583
-
-
VanHouten, J.N.1
Yu, N.2
Rimm, D.3
Dotto, J.4
Arnold, A.5
Wysolmerski, J.J.6
|