-
1
-
-
0000319647
-
Genetic aspects of adenomatosis of endocrine glands
-
Wermer, P. (1954) Genetic aspects of adenomatosis of endocrine glands. The American Journal of Medicine 16, 363-371.
-
(1954)
The American Journal of Medicine
, vol.16
, pp. 363-371
-
-
Wermer, P.1
-
3
-
-
0030963446
-
Positional cloning of the gene for multiple endocrine neoplasiatype 1
-
Chandrasekharappa, S.C., Guru, S.C., Manickam, P. et al. (1997) Positional cloning of the gene for multiple endocrine neoplasiatype 1. Science 276, 404-407.
-
(1997)
Science
, vol.276
, pp. 404-407
-
-
Chandrasekharappa, S.C.1
Guru, S.C.2
Manickam, P.3
-
4
-
-
33745125712
-
Tumor suppressor menin: The essential role of nuclear localization signal domains in coordinating gene expression
-
DOI 10.1038/sj.onc.1209400, PII 1209400
-
La, P., Desmond, A., Hou, Z. et al. (2006) Tumour suppressor menin: the essential role of nuclear localization signal domains in coordinating gene expression. Oncogene 25, 3537-3546. (Pubitemid 43901675)
-
(2006)
Oncogene
, vol.25
, Issue.25
, pp. 3537-3546
-
-
La, P.1
Desmond, A.2
Hou, Z.3
Silva, A.C.4
Schnepp, R.W.5
Hua, X.6
-
5
-
-
33847072634
-
In search of tumor suppressing functions of menin
-
DOI 10.1016/j.mce.2006.12.032, PII S0303720706005892, Adrenal/Molecular Steroidogenesis Conference 2006 AMS 2006
-
Yang, Y.&Hua, X. (2007) In search of tumour suppressing functions of menin. Molecular and Cellular Endocrinology 265-266, 34-41. (Pubitemid 46273978)
-
(2007)
Molecular and Cellular Endocrinology
, vol.265-266
, Issue.SUPPL.
, pp. 34-41
-
-
Yang, Y.1
Hua, X.2
-
6
-
-
33646474127
-
Genome-wide analysis of menin binding provides insights into MEN1 tumourigenesis
-
Scacheri, P.C., Davis, S., Odom, D.T. et al. (2006) Genome-wide analysis of menin binding provides insights into MEN1 tumourigenesis. PLoS Genetics 2, e51.
-
(2006)
PLoS Genetics
, vol.2
-
-
Scacheri, P.C.1
Davis, S.2
Odom, D.T.3
-
7
-
-
0038695861
-
Functional studies of the MEN1 gene
-
DOI 10.1046/j.1365-2796.2003.01165.x
-
Chandrasekharappa, S.C. & Teh, B.T. (2003) Functional studies of the MEN1 gene. Journal of Internal Medicine 253, 606-615. (Pubitemid 36649092)
-
(2003)
Journal of Internal Medicine
, vol.253
, Issue.6
, pp. 606-615
-
-
Chandrasekharappa, S.C.1
Teh, B.T.2
-
8
-
-
38149112594
-
Multiple endocrine neoplasia type 1 (MEN1): Analysis of 1336 mutations reported in the first decade following identification of the gene
-
Lemos, M.C. & Thakker, R.V. (2008) Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene. Human Mutation 29, 22-32.
-
(2008)
Human Mutation
, vol.29
, pp. 22-32
-
-
Lemos, M.C.1
Thakker, R.V.2
-
9
-
-
34548805701
-
Clinical testing for mutations in the MEN1 gene in Sweden: A report on 200 unrelated cases
-
DOI 10.1210/jc.2007-0476
-
Tham, E., Grandell, U., Lindgren, E. et al. (2007) Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases. Journal of Clinical Endocrinology and Metabolism 92, 3389-3395. (Pubitemid 47435311)
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, vol.92
, Issue.9
, pp. 3389-3395
-
-
Tham, E.1
Grandell, U.2
Lindgren, E.3
Toss, G.4
Skogseid, B.5
Nordenskjold, M.6
-
10
-
-
39149128288
-
Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1
-
DOI 10.1111/j.1365-2265.2007.03045.x
-
Owens, M., Ellard, S. & Vaidya, B. (2008) Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1. Clinical Endocrinology (Oxford) 68, 350-354. (Pubitemid 351257851)
-
(2008)
Clinical Endocrinology
, vol.68
, Issue.3
, pp. 350-354
-
-
Owens, M.1
Ellard, S.2
Vaidya, B.3
-
11
-
-
2342500422
-
Molecular pathology of the MEN1 gene
-
DOI 10.1196/annals.1294.020
-
Agarwal, S.K., Lee, B.A., Sukhodolets, K.E. et al. (2004) Molecular pathology of the MEN1 gene. Annals of the New York Academy of Sciences 1014, 189-198. (Pubitemid 38594805)
-
(2004)
Annals of the New York Academy of Sciences
, vol.1014
, pp. 189-198
-
-
Agarwal, S.K.1
Burns, A.L.2
Sukhodolets, K.E.3
Kennedy, P.A.4
Obungu, V.H.5
Hickman, A.B.6
Mullendore, M.E.7
Whitten, I.8
Skarulis, M.C.9
Simonds, W.F.10
Mateo, C.11
Crabtree, J.S.12
Scacheri, P.C.13
Ji, Y.14
Novotny, E.A.15
Garrett-Beal, L.16
Ward, J.M.17
Libutti, S.K.18
Alexander, H.R.19
Cerrato, A.20
Parisi, M.J.21
Anna-A, S.S.22
Oliver, B.23
Chandrasekharappa, S.C.24
Collins, F.S.25
Spiegel, A.M.26
Marx, S.J.27
more..
-
12
-
-
0141457540
-
Functional characterization of a promoter region in the human MEN1 tumor suppressor gene
-
DOI 10.1016/j.jmb.2003.08.001
-
Fromaget, M., Vercherat, C., Zhang, C.X. et al. (2003) Functional characterization of a promoter region in the human MEN1 tumour suppressor gene. Journal of Molecular Biology 333, 87-102. (Pubitemid 37153267)
-
(2003)
Journal of Molecular Biology
, vol.333
, Issue.1
, pp. 87-102
-
-
Fromaget, M.1
Vercherat, C.2
Zhang, C.X.3
Zablewska, B.4
Gaudray, P.5
Chayvialle, J.-A.6
Calender, A.7
Cordier-Bussat, M.8
-
13
-
-
0041381430
-
Transcription regulation of the multiple endocrine neoplasia type 1 gene in human and mouse
-
DOI 10.1210/jc.2003-030288
-
Zablewska, B., Bylund, L., Mandic, S.A. et al. (2003) Transcription regulation of the multiple endocrine neoplasia type 1 gene in human and mouse. Journal of Clinical Endocrinology and Metabolism 88, 3845-3851. (Pubitemid 37034537)
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, Issue.8
, pp. 3845-3851
-
-
Zablewska, B.1
Bylund, L.2
Mandic, S.A.3
Fromaget, M.4
Gaudray, P.5
Weber, G.6
-
14
-
-
0030010591
-
Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumours
-
Nakayama, K., Ishida, N., Shirane, M. et al. (1996) Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumours. Cell 85, 707-720.
-
(1996)
Cell
, vol.85
, pp. 707-720
-
-
Nakayama, K.1
Ishida, N.2
Shirane, M.3
-
15
-
-
33750361636
-
Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans
-
DOI 10.1073/pnas.0603877103
-
Pellegata, N.S., Quintanilla-Martinez, L., Siggelkow, H. et al. (2006) Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proceedings of the National Academy of Sciences of the United States of America 103, 15558-15563. (Pubitemid 44625631)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, 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
Fend, F.7
Graw, J.8
Atkinson, M.J.9
-
16
-
-
77952463207
-
Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumours
-
Molatore, S., Kiermaier, E., Jung, C.B. et al. (2010) Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumours. Molecular Cancer 9, 116.
-
(2010)
Molecular Cancer
, vol.9
, pp. 116
-
-
Molatore, S.1
Kiermaier, E.2
Jung, C.B.3
-
17
-
-
33847294682
-
Distribution of menin-occupied regions in chromatin specifies a broad role of menin in transcriptional regulation
-
Agarwal, S.K., Impey, S., McWeeney, S. et al. (2007) Distribution of menin-occupied regions in chromatin specifies a broad role of menin in transcriptional regulation. Neoplasia 9, 101-107.
-
(2007)
Neoplasia
, vol.9
, pp. 101-107
-
-
Agarwal, S.K.1
Impey, S.2
McWeeney, S.3
-
18
-
-
58549111025
-
Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor- interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations
-
Igreja, S., Chahal, H.S., Akker, S.A. et al. (2009) Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor- interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations. Clinical Endocrinology (Oxford) 70, 259-264.
-
(2009)
Clinical Endocrinology (Oxford)
, vol.70
, pp. 259-264
-
-
Igreja, S.1
Chahal, H.S.2
Akker, S.A.3
-
19
-
-
79951672207
-
p27kip1: A new multiple endocrine neoplasia gene?
-
Marinoni, I. & Pellegata, N.S. (2011) p27kip1: a new multiple endocrine neoplasia gene? Neuroendocrinology 93, 19-28.
-
(2011)
Neuroendocrinology
, vol.93
, pp. 19-28
-
-
Marinoni, I.1
Pellegata, N.S.2
-
20
-
-
77956581284
-
MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations
-
Georgitsi, M. (2010) MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations. Best Practice & Research Clinical Endocrinology & Metabolism 24, 425-437.
-
(2010)
Best Practice & Research Clinical Endocrinology & Metabolism
, vol.24
, pp. 425-437
-
-
Georgitsi, M.1
-
21
-
-
0034926789
-
Multiple endocrine neoplasia type 1: Genetic and clinical aspects
-
Calender, A., Cadiot, G. & Mignon, M. (2001) [Multiple endocrine neoplasia type 1: genetic and clinical aspects]. Gastroenterologie Clinique et Biologique 25(4 Suppl), B38-B48.
-
(2001)
Gastroenterologie Clinique et Biologique
, vol.25
, Issue.4 SUPPL.
-
-
Calender, A.1
Cadiot, G.2
Mignon, M.3
-
22
-
-
34249860559
-
Kip1 mutations
-
DOI 10.1210/jc.2006-2563
-
Ozawa, A., Agarwal, S.K., Mateo, C.M. et al. (2007) The parathyroid/ pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations. Journal of Clinical Endocrinology and Metabolism 92, 1948-1951. (Pubitemid 46997215)
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, 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
Quigley, C.M.7
Simonds, W.F.8
Weinstein, L.S.9
Chandrasekharappa, S.C.10
Collins, F.S.11
Spiegel, A.M.12
Marx, S.J.13
-
23
-
-
34447560185
-
Kip1 mutation in multiple endocrine neoplasia
-
DOI 10.1210/jc.2006-2843
-
Georgitsi, M., Raitila, A., Karhu, A. et al. (2007) Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia. Journal of Clinical Endocrinology and Metabolism 92, 3321-3325. (Pubitemid 47236408)
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, vol.92
, Issue.8
, pp. 3321-3325
-
-
Georgitsi, M.1
Raitila, A.2
Karhu, A.3
Van Der, L.R.B.4
Aalfs, C.M.5
Sane, T.6
Vierimaa, O.7
Makinen, M.J.8
Tuppurainen, K.9
Paschke, R.10
Gimm, O.11
Koch, C.A.12
Gundogdu, S.13
Lucassen, A.14
Tischkowitz, M.15
Izatt, L.16
Aylwin, S.17
Bano, G.18
Hodgson, S.19
De Menis, E.20
Launonen, V.21
Vahteristo, P.22
Aaltonen, L.A.23
more..
-
24
-
-
78651492268
-
Familial pituitary adenomas
-
Vandeva, S., Vasilev, V., Vroonen, L. et al. (2010) Familial pituitary adenomas. Annales d'endocrinologie (Paris) 71, 479-485.
-
(2010)
Annales d'Endocrinologie (Paris)
, vol.71
, pp. 479-485
-
-
Vandeva, S.1
Vasilev, V.2
Vroonen, L.3
-
25
-
-
77956572234
-
The genetics of pituitary adenomas
-
Vandeva, S., Jaffrain-Rea, M.L., Daly, A.F. et al. (2010) The genetics of pituitary adenomas. Best Practice & Research Clinical Endocrinology & Metabolism 24, 461-476.
-
(2010)
Best Practice & Research Clinical Endocrinology & Metabolism
, vol.24
, pp. 461-476
-
-
Vandeva, S.1
Jaffrain-Rea, M.L.2
Daly, A.F.3
-
26
-
-
33744486595
-
Pituitary adenoma predisposition caused by germline mutations in the AIP gene
-
DOI 10.1126/science.1126100
-
Vierimaa, O., Georgitsi, M., Lehtonen, R. et al. (2006) Pituitary adenoma predisposition caused by germline mutations in the AIP gene. Science 312, 1228-1230. (Pubitemid 43801151)
-
(2006)
Science
, vol.312
, Issue.5777
, pp. 1228-1230
-
-
Vierimaa, O.1
Georgitsi, M.2
Lehtonen, R.3
Vahteristo, P.4
Kokko, A.5
Raitila, A.6
Tuppurainen, K.7
Ebeling, T.M.L.8
Salmela, P.I.9
Paschke, R.10
Gundogdu, S.11
De Menis, E.12
Makinen, M.J.13
Launonen, V.14
Karhu, A.15
Aaltonen, L.A.16
-
27
-
-
53749085204
-
Large genomic deletions in AIP in pituitary adenoma predisposition
-
Georgitsi, M., Heliovaara, E., Paschke, R. et al. (2008) Large genomic deletions in AIP in pituitary adenoma predisposition. Journal of Clinical Endocrinology and Metabolism 93, 4146-4151.
-
(2008)
Journal of Clinical Endocrinology and Metabolism
, vol.93
, pp. 4146-4151
-
-
Georgitsi, M.1
Heliovaara, E.2
Paschke, R.3
-
28
-
-
85047682409
-
Consensus: Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
DOI 10.1210/jc.86.12.5658
-
Brandi, M.L., Gagel, R.F., Angeli, A. et al. (2001) Guidelines for diagnosis and therapy of MEN type 1 and type 2. Journal of Clinical Endocrinology and Metabolism 86, 5658-5671. (Pubitemid 33152604)
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, 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
Conte-Devolx, B.7
Falchetti, A.8
Gheri, R.G.9
Libroia, A.10
Lips, C.J.M.11
Lombardi, G.12
Mannelli, M.13
Pacini, F.14
Ponder, B.A.J.15
Raue, F.16
Skogseid, B.17
Tamburrano, G.18
Thakker, R.V.19
Thompson, N.W.20
Tomassetti, P.21
Tonelli, F.22
Wells Jr., S.A.23
Marx, S.J.24
more..
-
29
-
-
74049094783
-
Diagnostic challenges due to phenocopies: Lessons from Multiple Endocrine Neoplasia type1 (MEN1)
-
Turner, J.J., Christie, P.T., Pearce, S.H. et al. (2010) Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1). Human Mutation 31, E1089-E1101.
-
(2010)
Human Mutation
, vol.31
-
-
Turner, J.J.1
Christie, P.T.2
Pearce, S.H.3
-
30
-
-
77956634043
-
The MENX syndrome and p27: Relationships with multiple endocrine neoplasia
-
Molatore, S. & Pellegata, N.S. (2010) The MENX syndrome and p27: relationships with multiple endocrine neoplasia. Progress in Brain Research 182, 295-320.
-
(2010)
Progress in Brain Research
, vol.182
, pp. 295-320
-
-
Molatore, S.1
Pellegata, N.S.2
-
31
-
-
35548967589
-
The clinical, pathological, and genetic features of familial isolated pituitary adenomas
-
DOI 10.1530/EJE-07-0348
-
Beckers, A. & Daly, A.F. (2007) The clinical, pathological, and genetic features of familial isolated pituitary adenomas. European Journal of Endocrinology 157, 371-382. (Pubitemid 350018439)
-
(2007)
European Journal of Endocrinology
, vol.157
, Issue.4
, pp. 371-382
-
-
Beckers, A.1
Daly, A.F.2
-
32
-
-
34249862215
-
Germline mutation in the aryl hydrocarbon receptor interacting protein gene in familial somatotropinoma
-
DOI 10.1210/jc.2006-2394
-
Toledo, R.A., Lourenco D.M. Jr, Liberman, B. et al. (2007) Germline mutation in the aryl hydrocarbon receptor interacting protein gene in familial somatotropinoma. Journal of Clinical Endocrinology and Metabolism 92, 1934-1937. (Pubitemid 46997212)
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, vol.92
, Issue.5
, pp. 1934-1937
-
-
Toledo, R.A.1
Lourenco Jr., D.M.2
Liberman, B.3
Cunha-Neto, M.B.C.4
Cavalcanti, M.G.5
Moyses, C.B.6
Toledo, S.P.A.7
Dahia, P.L.M.8
-
33
-
-
77953595980
-
Isolated familial somatotropinoma: 11q13-loh and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumourigenesis
-
Toledo, R.A., Mendonca, B.B., Fragoso, M.C. et al. (2010) Isolated familial somatotropinoma: 11q13-loh and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumourigenesis. Clinics (Sao Paulo) 65, 407-415.
-
(2010)
Clinics (Sao Paulo)
, vol.65
, pp. 407-415
-
-
Toledo, R.A.1
Mendonca, B.B.2
Fragoso, M.C.3
-
34
-
-
0032787809
-
Genetic and clinical analysis in 10 Spanish patients with multiple endocrine neoplasia type 1
-
DOI 10.1038/sj.ejhg.5200336
-
Cebrian, A. et al. (1999) Genetic and clinical analysis in 10 Spanish patients with multiple endocrine neoplasia type 1. European Journal of Human Genetics, 7, 585-589. (Pubitemid 29378035)
-
(1999)
European Journal of Human Genetics
, vol.7
, Issue.5
, pp. 585-589
-
-
Cebrian, A.1
Herrera-Pombo, J.L.2
Diez, J.J.3
Sanchez-Vilar, O.4
Lara, J.I.5
Vazquez, C.6
Pico, A.7
Osorio, A.8
Martinez-Delgado, B.9
Benitez, J.10
Robledo, M.11
-
35
-
-
0041777670
-
Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients
-
Cebrian, A. et al. (2003) Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients. Journal of Medical Genetics, 40, e72.
-
(2003)
Journal of Medical Genetics
, vol.40
-
-
Cebrian, A.1
-
36
-
-
0032231708
-
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders
-
DOI 10.1086/301953
-
Giraud, S. et al. (1998) Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders. American Journal of Human Genetics, 63, 455-467. (Pubitemid 30418627)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.2
, pp. 455-467
-
-
Giraud, S.1
Zhang, C.X.2
Serova-Sinilnikova, O.3
Wautot, V.4
Salandre, J.5
Buisson, N.6
Waterlot, C.7
Bauters, C.8
Porchet, N.9
Aubert, J.-P.10
Emy, P.11
Cadiot, G.12
Delemer, B.13
Chabre, O.14
Niccoli, P.15
Leprat, F.16
Duron, F.17
Emperauger, B.18
Cougard, P.19
Goudet, P.20
Sarfati, E.21
Riou, J.-P.22
Guichard, S.23
Rodier, M.24
Meyrier, A.25
Caron, P.26
Vantyghem, M.-C.27
Assayag, M.28
Peix, J.-L.29
Pugeat, M.30
Rohmer, V.31
Vallotton, M.32
Lenoir, G.33
Gaudray, P.34
Proye, C.35
Conte-Devolx, B.36
Chanson, P.37
Shugart, Y.Y.38
Goldgar, D.39
Murat, A.40
Calender, A.41
more..
-
37
-
-
0035973079
-
10 Swiss kindreds with multiple endocrine neoplasia type 1: Assessment of screening methods
-
Clerici, T. et al. (2001) 10 Swiss kindreds with multiple endocrine neoplasia type 1: assessment of screening methods. Swiss Medical Weekly, 131, 381-386. (Pubitemid 32750871)
-
(2001)
Swiss Medical Weekly
, vol.131
, Issue.25-26
, pp. 381-386
-
-
Clerici, T..1
Schmid, C..2
Komminoth, P.3
Lange, J.4
Spinas, G.A.5
Brandle, M.6
-
38
-
-
0030963446
-
Positional cloning of the gene for multiple endocrine neoplasia-type 1
-
Chandrasekharappa, S.C. et al. (1997) Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science, 276, 404-407.
-
(1997)
Science
, vol.276
, pp. 404-407
-
-
Chandrasekharappa, S.C.1
-
39
-
-
8544266010
-
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene
-
DOI 10.1093/hmg/6.7.1177
-
Lemmens, I. et al. (1997) Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1. Human Molecular Genetics, 6, 1177-1183. (Pubitemid 27308405)
-
(1997)
Human Molecular Genetics
, vol.6
, Issue.7
, pp. 1177-1183
-
-
Lemmens, I.1
Van De, V.W.J.M.2
Kas, K.3
Zhang, C.X.4
Giraud, S.5
Wautot, V.6
Buisson, N.7
De Witte, K.8
Salandre, J.9
Lenoir, G.10
Pugeat, M.11
Calender, A.12
Parente, F.13
Quincey, D.14
Gaudray, P.15
De Wit, M.J.16
Lips, C.J.M.17
Hoppener, J.W.M.18
Khodaei, S.19
Grant, A.L.20
Weber, G.21
Kytola, S.22
Teh, B.T.23
Farnebo, F.24
Phelan, C.25
Hayward, N.26
Larsson, C.27
Pannett, A.A.J.28
Forbes, S.A.29
Bassett, J.H.D.30
Thakker, R.V.31
more..
-
40
-
-
15144346400
-
Alterations of the MEN1 gene in sporadic parathyroid tumors
-
DOI 10.1210/jc.83.8.2627
-
Farnebo, F. et al. (1998) Alterations of the MEN1 gene in sporadic parathyroid tumors. Journal of Clinical Endocrinology and Metabolism, 83, 2627-2630. (Pubitemid 28493751)
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, 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
Thompson, N.W.7
Hoog, A.8
Weber, G.9
Farnebo, L.-O.10
Larsson, C.11
-
41
-
-
13844318139
-
Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory
-
DOI 10.1097/01.GIM.0000153663.62300.F8
-
Klein, R.D., Salih, S., Bessoni, J. et al. (2005) Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory. Genetics in Medicine, 7, 131-138. (Pubitemid 40261839)
-
(2005)
Genetics in Medicine
, vol.7
, Issue.2
, pp. 131-138
-
-
Klein, R.D.1
Salih, S.2
Bessoni, J.3
Bale, A.E.4
-
42
-
-
0031756105
-
Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidism
-
DOI 10.1002/(SICI)1096-8628(19981116)80:3<221::AID-AJMG8>3.0.CO;2-1
-
Fujimori, M. et al. (1998) Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidism. American Journal of Medical Genetics, 80, 221-222. (Pubitemid 28533532)
-
(1998)
American Journal of Medical Genetics
, vol.80
, Issue.3
, pp. 221-222
-
-
Fujimori, M.1
Shirahama, S.2
Sakurai, A.3
Hashizume, K.4
Hama, Y.5
Ito, K.-I.6
Shingu, K.7
Kobayashi, S.8
Amano, J.9
Fukushima, Y.10
-
43
-
-
0031725337
-
Menin mutations in MEN1 patients
-
Mayr, B., Brabant, G. & von zur, M.A. (1998) Menin mutations in MEN1 patients. Journal of Clinical Endocrinology and Metabolism, 83, 3004-3005.
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, pp. 3004-3005
-
-
Mayr, B.1
Brabant, G.2
Von Zur, M.A.3
-
44
-
-
17344363260
-
Characterization of mutations in patients with multiple endocrine neoplasia type 1
-
DOI 10.1086/301729
-
Bassett, J.H. et al. (1998) Characterization of mutations in patients with multiple endocrine neoplasia type 1. American Journal of Human Genetics, 62, 232-244. (Pubitemid 28110764)
-
(1998)
American Journal of Human Genetics
, vol.62
, Issue.2
, pp. 232-244
-
-
Bassett, J.H.D.1
Forbes, S.A.2
Pannett, A.A.J.3
Lloyd, S.E.4
Christie, P.T.5
Wooding, C.6
Harding, B.7
Besser, G.M.8
Edwards, C.R.9
Monson, J.P.10
Sampson, J.11
Wass, J.A.H.12
Wheeler, M.H.13
Thakker, R.V.14
-
45
-
-
8544279953
-
Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states
-
DOI 10.1093/hmg/6.7.1169
-
Agarwal, S.K. et al. (1997) Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Human Molecular Genetics, 6, 1169-1175. (Pubitemid 27308404)
-
(1997)
Human Molecular Genetics
, vol.6
, Issue.7
, pp. 1169-1175
-
-
Agarwal, S.K.1
Kester, M.B.2
Debelenko, L.V.3
Heppner, C.4
Emmert-Buck, M.R.5
Skarulis, M.C.6
Doppman, J.L.7
Kim, Y.S.8
Lubensky, I.A.9
Zhuang, Z.10
Green, J.S.11
Guru, S.C.12
Manickam, P.13
Olufemi, S.-E.14
Liotta, L.A.15
Chandrasekharappa, S.C.16
Collins, F.S.17
Spiegel, A.M.18
Lee, B.A.19
Marx, S.J.20
more..
-
46
-
-
0032920224
-
Multiple endocrine neoplasia type 1 (MEN1): Clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop)
-
DOI 10.1046/j.1365-2265.1999.00648.x
-
Valdes, N. et al. (1999) Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop). Clinical Endocrinology (Oxford), 50, 309-313. (Pubitemid 29166709)
-
(1999)
Clinical Endocrinology
, vol.50
, Issue.3
, pp. 309-313
-
-
Valdes, N.1
Perez, D.N.G.2
Alvarez, V.3
Castano, L.4
Diaz-Cadorniga, F.5
Aller, J.6
Coto, E.7
-
47
-
-
19944430556
-
A report of a national mutation testing service for the MEN1 gene: Clinical presentations and implications for mutation testing
-
DOI 10.1136/jmg.2003.017319
-
Cardinal, J.W. et al. (2005) A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing. Journal of Medical Genetics, 42, 69-74. (Pubitemid 40187124)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.1
, pp. 69-74
-
-
Cardinal, J.W.1
Bergman, L.2
Hayward, N.3
Sweet, A.4
Warner, J.5
Marks, L.6
Learoyd, D.7
Dwight, T.8
Robinson, B.9
Epstein, M.10
Smith, M.11
Teh, B.T.12
Cameron, D.P.13
Prins, J.B.14
-
48
-
-
0036232062
-
Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions
-
DOI 10.1046/j.1365-2265.2002.01505.x
-
Cavaco, B.M. et al. (2002) Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions. Clinical Endocrinology (Oxford), 56, 465-473. (Pubitemid 34429621)
-
(2002)
Clinical Endocrinology
, vol.56
, Issue.4
, pp. 465-473
-
-
Cavaco, B.M.1
Domingues, R.2
Bacelar, M.C.3
Cardoso, H.4
Barros, L.5
Gomes, L.6
Ruas, M.M.A.7
Agapito, A.8
Garrao, A.9
Pannett, A.A.J.10
Silva, J.L.11
Sobrinho, L.G.12
Thakker, R.V.13
Leite, V.14
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