-
1
-
-
0028204821
-
Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma
-
Abstract
-
Cryns, V.L., Thor, A., Xu Xu, S., Wierman, M.E., Vickery, A.L.J., Benedict, W.F. & Arnold, A. (1994) Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma. New England Journal of Medicine, 330, 757-761. (Abstract)
-
(1994)
New England Journal of Medicine
, vol.330
, pp. 757-761
-
-
Cryns, V.L.1
Thor, A.2
Xu Xu, S.3
Wierman, M.E.4
Vickery, A.L.J.5
Benedict, W.F.6
Arnold, A.7
-
2
-
-
0029010785
-
Frequent loss of chromosome arm 1p DNA in parathyroid adenomas
-
Cryns, V.L., Yi, S.M., Tahara, H., Gaz, R.D. & Arnold, A. (1995) Frequent loss of chromosome arm 1p DNA in parathyroid adenomas. Genes, Chromosomes Cancer, 13, 9-17.
-
(1995)
Genes, Chromosomes Cancer
, vol.13
, pp. 9-17
-
-
Cryns, V.L.1
Yi, S.M.2
Tahara, H.3
Gaz, R.D.4
Arnold, A.5
-
3
-
-
0027303248
-
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
-
Donis-Keller, H., Dou, S., Chi, D., Carlson, K.M., Toshima, K., Lairmore, T.C., Howe, J.R., Moley, J.F., Goodfellow, P. & Wells, S.A. (1993) Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Human Molecular Genetics, 2, 851-856.
-
(1993)
Human Molecular Genetics
, vol.2
, pp. 851-856
-
-
Donis-Keller, H.1
Dou, S.2
Chi, D.3
Carlson, K.M.4
Toshima, K.5
Lairmore, T.C.6
Howe, J.R.7
Moley, J.F.8
Goodfellow, P.9
Wells, S.A.10
-
4
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon, E.R. & Vogelstein, B. (1990) A genetic model for colorectal tumorigenesis. Cell, 61, 759-767.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
5
-
-
0027136050
-
Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: Results of long-term follow-up
-
Howe, J.R., Norton, J.A. & Wells, S.A. (1993) Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: results of long-term follow-up. Surgery, 114(6), 1070-1077.
-
(1993)
Surgery
, vol.114
, Issue.6
, pp. 1070-1077
-
-
Howe, J.R.1
Norton, J.A.2
Wells, S.A.3
-
6
-
-
0028196667
-
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families
-
McMahon, R., Mulligan, L.M., Healey, C.S., Payne, S.J., Ponder, M., Ferguson-Smith, M.A., Barton, D.E. & Ponder, B.A.J. (1994) Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families. Human Molecular Genetics, 3, 643-646.
-
(1994)
Human Molecular Genetics
, vol.3
, pp. 643-646
-
-
McMahon, R.1
Mulligan, L.M.2
Healey, C.S.3
Payne, S.J.4
Ponder, M.5
Ferguson-Smith, M.A.6
Barton, D.E.7
Ponder, B.A.J.8
-
7
-
-
0027231568
-
Germline mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan, L.M., Kwok, J.B.J., Healey, C.S., Elsdon, M.J., Eng, C., Gardner, E., Love, D.R., Mole, S.E., Moore, J.K., Papi, L., Ponder, M.A., Telenius, H., Tunnacliffe, A. & Ponder, B.A.J. (1993) Germline mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature, 363, 458-460.
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.J.2
Healey, C.S.3
Elsdon, M.J.4
Eng, C.5
Gardner, E.6
Love, D.R.7
Mole, S.E.8
Moore, J.K.9
Papi, L.10
Ponder, M.A.11
Telenius, H.12
Tunnacliffe, A.13
Ponder, B.A.J.14
-
8
-
-
0028199074
-
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FTMC
-
Mulligan, L.M., Eng, C., Healey, C.S., Clayton, D., Kwok, J.B.J., Gardner, E., Ponder, M.A., Frilling, A., Jackson, C.E., Lehnert, H., Neumann, H.P.H.,Thibodeau, S.N. & Ponder, B.A.J. (1994) Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FTMC. Nature Genetics, 6, 70-74.
-
(1994)
Nature Genetics
, vol.6
, pp. 70-74
-
-
Mulligan, L.M.1
Eng, C.2
Healey, C.S.3
Clayton, D.4
Kwok, J.B.J.5
Gardner, E.6
Ponder, M.A.7
Frilling, A.8
Jackson, C.E.9
Lehnert, H.10
Neumann, H.P.H.11
Thibodeau, S.N.12
Ponder, B.A.J.13
-
9
-
-
15844383259
-
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of u-calpain as the multiple endocrine neoplasia type 1 gene
-
Pang, J.T., Lloyd, S.E., Wooding, C., Farren, B., Pottinger, B., Harding, B., Leigh, S.E.A., Pook, M.A., Benham, F.J., Gillet, G.T., Taggert, R.T. & Thakker, R.V.C. (1996) Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of u-calpain as the multiple endocrine neoplasia type 1 gene. Human Genetics, 97, 732-741.
-
(1996)
Human Genetics
, vol.97
, pp. 732-741
-
-
Pang, J.T.1
Lloyd, S.E.2
Wooding, C.3
Farren, B.4
Pottinger, B.5
Harding, B.6
Leigh, S.E.A.7
Pook, M.A.8
Benham, F.J.9
Gillet, G.T.10
Taggert, R.T.11
Thakker, R.V.C.12
-
10
-
-
0029818901
-
Loss of heterozygosity studies of the retinoblastoma gene and breast cancer susceptibility (BRCA2) loci in pituitary, parathyroid, pancreatic and carcinoid tumours
-
Pearce, S.H., Trump, D., Wooding, C., Sheppard, M.N., Clayton, R.N. & Thakker, R.V. (1996) Loss of heterozygosity studies of the retinoblastoma gene and breast cancer susceptibility (BRCA2) loci in pituitary, parathyroid, pancreatic and carcinoid tumours. Clinical Endocrinology, 45, 195-200.
-
(1996)
Clinical Endocrinology
, vol.45
, pp. 195-200
-
-
Pearce, S.H.1
Trump, D.2
Wooding, C.3
Sheppard, M.N.4
Clayton, R.N.5
Thakker, R.V.6
-
11
-
-
0014331669
-
Study of a kindred of phaeochromocytoma, MTC, hyperparathyroidism and Cushing's disease: Multiple endocrine neoplasia type 2
-
Steiner, A.L., Goodman, A.D. & Powers, S.R. (1968) Study of a kindred of phaeochromocytoma, MTC, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia type 2. Medicine, 47, 371-409.
-
(1968)
Medicine
, vol.47
, pp. 371-409
-
-
Steiner, A.L.1
Goodman, A.D.2
Powers, S.R.3
-
12
-
-
0028958106
-
Hereditary hyperparathyroidism-jaw tumor syndrome: The endocrine tumour gene HRPT2 maps to chromosome 1q21-q31
-
Szabo, J., Heath, B., Hill, V.M., Jackson, C.E., Zarbo, R.J., Mallette, L.E., Chew, S.L., Besser, G.M., Thakker, R.V., Huff, V., Leppert, M.F. & Heath, H.I. (1995) Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumour gene HRPT2 maps to chromosome 1q21-q31. American Journal of Human Genetics, 56, 944-950.
-
(1995)
American Journal of Human Genetics
, vol.56
, pp. 944-950
-
-
Szabo, J.1
Heath, B.2
Hill, V.M.3
Jackson, C.E.4
Zarbo, R.J.5
Mallette, L.E.6
Chew, S.L.7
Besser, G.M.8
Thakker, R.V.9
Huff, V.10
Leppert, M.F.11
Heath, H.I.12
-
13
-
-
0027397923
-
The molecular genetics of the multiple endocrine neoplasia syndromes
-
Thakker, R.V. (1993) The molecular genetics of the multiple endocrine neoplasia syndromes. Clinical Endocrinology, 38, 1-14.
-
(1993)
Clinical Endocrinology
, vol.38
, pp. 1-14
-
-
Thakker, R.V.1
-
14
-
-
0027161684
-
Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations
-
Thakker, R.V., Pook, M.A., Wooding, C., Boscaro, M., Scanarini, M. & Clayton, R.N. (1993) Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. Journal of Clinical Investigation, 91, 2815-2821.
-
(1993)
Journal of Clinical Investigation
, vol.91
, pp. 2815-2821
-
-
Thakker, R.V.1
Pook, M.A.2
Wooding, C.3
Boscaro, M.4
Scanarini, M.5
Clayton, R.N.6
-
15
-
-
6844250962
-
Localisation of a tumour suppressor gene causing parathyroid tumours to chromosome 1p34-p36
-
Williamson, C., Pannett, A., Pang, J.T., McCarthy, M., Monson, J.P. & Thakker, R.V. (1995) Localisation of a tumour suppressor gene causing parathyroid tumours to chromosome 1p34-p36. Journal of Bone and Mineral Research, 10(supp 1), 64.
-
(1995)
Journal of Bone and Mineral Research
, vol.10
, Issue.1 SUPPL.
, pp. 64
-
-
Williamson, C.1
Pannett, A.2
Pang, J.T.3
McCarthy, M.4
Monson, J.P.5
Thakker, R.V.6
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