-
1
-
-
0023449599
-
Familial multiple endocrine neoplasia type 1: A new look at pathophysiology
-
Brandi ML, Marx SJ, Aurbach GD, Fitzpatrick LA. 1987 Familial multiple endocrine neoplasia type 1: a new look at pathophysiology. Endocr Rev. 8:391-405.
-
(1987)
Endocr Rev
, vol.8
, pp. 391-405
-
-
Brandi, M.L.1
Marx, S.J.2
Aurbach, G.D.3
Fitzpatrick, L.A.4
-
2
-
-
0023828816
-
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
-
Larsson C, Skogseid B, Öberg K, Nakamura Y, Nordenskjöld M. 1988 Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature. 332:85-87.
-
(1988)
Nature
, vol.332
, pp. 85-87
-
-
Larsson, C.1
Skogseid, B.2
Öberg, K.3
Nakamura, Y.4
Nordenskjöld, M.5
-
3
-
-
0024399727
-
Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1
-
Friedman E, Sakaguchi K, Bale AE, et al. 1989 Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1. N Engl J Med. 321:213-218.
-
(1989)
N Engl J Med
, vol.321
, pp. 213-218
-
-
Friedman, E.1
Sakaguchi, K.2
Bale, A.E.3
-
4
-
-
0024399557
-
Multiple endocrine neoplasia type 1 (MEN-1)
-
Oberg K, Skogseid B, Eriksson B. 1989 Multiple endocrine neoplasia type 1 (MEN-1). Acta Oncol. 28:383-387.
-
(1989)
Acta Oncol
, vol.28
, pp. 383-387
-
-
Oberg, K.1
Skogseid, B.2
Eriksson, B.3
-
5
-
-
0024394627
-
Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11
-
Thakker RV, Bouloux P, Wooding C, et al. 1989 Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11. N Engl J Med. 321:60-68.
-
(1989)
N Engl J Med
, vol.321
, pp. 60-68
-
-
Thakker, R.V.1
Bouloux, P.2
Wooding, C.3
-
6
-
-
0025265337
-
Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors
-
Bystrom C, Larsson C, Blomberg C, et al. 1990 Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors. Proc Natl Acad Sci USA. 87:1968-1972.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 1968-1972
-
-
Bystrom, C.1
Larsson, C.2
Blomberg, C.3
-
7
-
-
0028908904
-
RFLP analysis of human chromosome 11 region q13 in multiple symmetric lipomatosis and multiple endocrine neoplasia type 1-associated lipomas
-
Morelli A, Falchetti A, Weinstein L, et al. 1995 RFLP analysis of human chromosome 11 region q13 in multiple symmetric lipomatosis and multiple endocrine neoplasia type 1-associated lipomas. Biochem Biophys Res Commun. 207:363-368.
-
(1995)
Biochem Biophys Res Commun
, vol.207
, pp. 363-368
-
-
Morelli, A.1
Falchetti, A.2
Weinstein, L.3
-
8
-
-
0027491108
-
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1)
-
Brandi ML, Weber G, Svensson A, et al. 1993 Homozygotes for the autosomal dominant neoplasia syndrome (MEN1). Am J Hum Genet. 53:1167-1172.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1167-1172
-
-
Brandi, M.L.1
Weber, G.2
Svensson, A.3
-
9
-
-
0015834582
-
Isolation of high molecular-weight DNA from mammalian cells
-
Gross-Bellard J, Oudet P, Chambon P. 1973 Isolation of high molecular-weight DNA from mammalian cells. Eur J Biochem. 36:32-38.
-
(1973)
Eur J Biochem
, vol.36
, pp. 32-38
-
-
Gross-Bellard, J.1
Oudet, P.2
Chambon, P.3
-
10
-
-
0023665343
-
A rapid method for the purification of DNA from blood
-
Jeanpierre M. 1987 A rapid method for the purification of DNA from blood. Nucleic Acids Res. 15:9615.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 9615
-
-
Jeanpierre, M.1
-
11
-
-
0027468554
-
Dinucleotide repeat polymorphism at the D11S480 locus
-
Moffat MF. 1993 Dinucleotide repeat polymorphism at the D11S480 locus. Hum Mol Genet. 2:492.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 492
-
-
Moffat, M.F.1
-
12
-
-
0026523066
-
A minisatellite and a microsatellite polymorphism within 1.5 Kb at the human muscle glycogen phosphorylnse (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95
-
Iwasaki H, Stewart PW, Dilley WG, et al. 1992 A minisatellite and a microsatellite polymorphism within 1.5 Kb at the human muscle glycogen phosphorylnse (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95. Genomics. 13:7-15.
-
(1992)
Genomics
, vol.13
, pp. 7-15
-
-
Iwasaki, H.1
Stewart, P.W.2
Dilley, W.G.3
-
13
-
-
0025947340
-
Isolation, localization and physical mapping of a highly polymorphic locus on human chromosome 11q13
-
Eubanks JH, Selleri L, Hart R, Rosette C, Evans GA. 1991 Isolation, localization and physical mapping of a highly polymorphic locus on human chromosome 11q13. Genomics. 11:720-729.
-
(1991)
Genomics
, vol.11
, pp. 720-729
-
-
Eubanks, J.H.1
Selleri, L.2
Hart, R.3
Rosette, C.4
Evans, G.A.5
-
14
-
-
0030040625
-
Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas
-
Tahara H, Smith AP, Gaz RD, et al. 1996 Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas. Cancer Res. 56:599-605.
-
(1996)
Cancer Res
, vol.56
, pp. 599-605
-
-
Tahara, H.1
Smith, A.P.2
Gaz, R.D.3
-
15
-
-
0026589155
-
Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13
-
Young RP, Sharp PA, Lynch JR, et al. 1992 Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13. J Med Genet. 29:236-238.
-
(1992)
J Med Genet
, vol.29
, pp. 236-238
-
-
Young, R.P.1
Sharp, P.A.2
Lynch, J.R.3
-
16
-
-
0028555313
-
Histologic features of parathyroid hyperplasia in multiple endocrine neoplasia type I. Diagnostic and surgical implications
-
Amorosi A, Nesi G, Spini S, Tonelli F, Falchetti A, Brandi ML. 1994 Histologic features of parathyroid hyperplasia in multiple endocrine neoplasia type I. Diagnostic and surgical implications. Acta Chir Austriaca. [Suppl 112]26:13-15.
-
(1994)
Acta Chir Austriaca. [Suppl 112]
, vol.26
, pp. 13-15
-
-
Amorosi, A.1
Nesi, G.2
Spini, S.3
Tonelli, F.4
Falchetti, A.5
Brandi, M.L.6
-
17
-
-
8544221951
-
Multiple endocrine neoplasia type 1: A model for the analysis of tumor clonality and its biological significance
-
Brandi ML, White R, eds. New York: Raven Press
-
Amorosi A, Cicchi P, Tonelli F, Brandi ML. 1991 Multiple endocrine neoplasia type 1: a model for the analysis of tumor clonality and its biological significance. In: Brandi ML, White R, eds. Hereditary tumors. New York: Raven Press; 89-98.
-
(1991)
Hereditary Tumors
, pp. 89-98
-
-
Amorosi, A.1
Cicchi, P.2
Tonelli, F.3
Brandi, M.L.4
-
18
-
-
0027434702
-
Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11
-
Falchetti A, Bale AE, Amorosi A, et al. 1993 Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11. J Clin Endocrinol Metab. 76:139-144.
-
(1993)
J Clin Endocrinol Metab
, vol.76
, pp. 139-144
-
-
Falchetti, A.1
Bale, A.E.2
Amorosi, A.3
-
19
-
-
0023022848
-
The parathyroid gland in health and disease
-
Ghandur-Mnaymneh L, Cassady J, Hajianpour MA, Paz J, Reiss E. 1986 The parathyroid gland in health and disease. Am J Hum Pathol. 125:292-299.
-
(1986)
Am J Hum Pathol
, vol.125
, pp. 292-299
-
-
Ghandur-Mnaymneh, L.1
Cassady, J.2
Hajianpour, M.A.3
Paz, J.4
Reiss, E.5
-
20
-
-
0026895234
-
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
-
Stone EM, Nichols BE, Streb LM, Kimura AE, Sheffield VC. 1992a Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13. Nat Genet. 1:246-250.
-
(1992)
Nat Genet
, vol.1
, pp. 246-250
-
-
Stone, E.M.1
Nichols, B.E.2
Streb, L.M.3
Kimura, A.E.4
Sheffield, V.C.5
-
21
-
-
0027018441
-
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13
-
Stone EM, Kimura AE, Folk JC, et al. 1992b Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13. Hum Mol Genet. 1:685-689.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 685-689
-
-
Stone, E.M.1
Kimura, A.E.2
Folk, J.C.3
-
22
-
-
0026662677
-
The gene for Best's macular dystrophy is located at 11q13 in a Swedish family
-
Forsman K, Graff C, Nordstrom S, et al. 1992 The gene for Best's macular dystrophy is located at 11q13 in a Swedish family. Clin Genet. 42:156-159.
-
(1992)
Clin Genet
, vol.42
, pp. 156-159
-
-
Forsman, K.1
Graff, C.2
Nordstrom, S.3
-
23
-
-
0026756530
-
The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533
-
Li Y, Muller B, Fuhrman C, et al. 1992 The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533. Am J Hum Genet. 51:749-754.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 749-754
-
-
Li, Y.1
Muller, B.2
Fuhrman, C.3
-
24
-
-
0028128537
-
Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous
-
Leppert M, Baird L, Anderson K, Otterud B, Lupski JR, Lewis RA. 1992 Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous. Nat Genet. 7:108-112.
-
(1992)
Nat Genet
, vol.7
, pp. 108-112
-
-
Leppert, M.1
Baird, L.2
Anderson, K.3
Otterud, B.4
Lupski, J.R.5
Lewis, R.A.6
-
25
-
-
0029010785
-
Frequent loss of chromosome arm 1p DNA in parathyroid adenomas
-
Cryns V, Yi SM, Tahara H, Gaz RD, Arnold A. 1992 Frequent loss of chromosome arm 1p DNA in parathyroid adenomas. Genes Chromosom Cancer. 13:9-17.
-
(1992)
Genes Chromosom Cancer
, vol.13
, pp. 9-17
-
-
Cryns, V.1
Yi, S.M.2
Tahara, H.3
Gaz, R.D.4
Arnold, A.5
-
26
-
-
0027944348
-
Variable regions of chromosome 11 loss in different pathological tissues of a patient with the multiple endocrine neoplasia type 1 syndrome
-
Beckers A, Abs R, Reyniers E, et al. 1994 Variable regions of chromosome 11 loss in different pathological tissues of a patient with the multiple endocrine neoplasia type 1 syndrome. J Clin Endocrinol Metab. 79:1498-1502.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 1498-1502
-
-
Beckers, A.1
Abs, R.2
Reyniers, E.3
-
27
-
-
0027015438
-
Sublocalization of multiple endocrine neoplasia type 1 gene
-
Larsson C, Weber G, Janson M. 1992 Sublocalization of multiple endocrine neoplasia type 1 gene. Henry Ford Hosp Med J. 40(Nos 3 & 4):159-161.
-
(1992)
Henry Ford Hosp Med J
, vol.40
, Issue.3-4
, pp. 159-161
-
-
Larsson, C.1
Weber, G.2
Janson, M.3
-
28
-
-
0030298007
-
Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13
-
Courseaux A, Grosgeorge J, Gaudray P, et al. 1996 Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. Cenomics. 37:354-365.
-
(1996)
Cenomics
, vol.37
, pp. 354-365
-
-
Courseaux, A.1
Grosgeorge, J.2
Gaudray, P.3
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