-
1
-
-
0017823411
-
Non-random centromere division: A mechanism of non-disjunction causing aneuploidy?
-
Méhes K. Non-random centromere division. a mechanism of non-disjunction causing aneuploidy? Hum Hered. 28:1978;255-260.
-
(1978)
Hum Hered
, vol.28
, pp. 255-260
-
-
Méhes, K.1
-
2
-
-
0020546228
-
Sequence of centromere separation: Occurrence, possible significance, and control
-
Vig B.K. Sequence of centromere separation. occurrence, possible significance, and control Cancer Genet Cytogenet. 8:1983;249-274.
-
(1983)
Cancer Genet Cytogenet
, vol.8
, pp. 249-274
-
-
Vig, B.K.1
-
3
-
-
0022631771
-
Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD)
-
Fitzgerald P.H., Archer S.A., Morris C.M. Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD). Hum Genet. 72:1986;58-62.
-
(1986)
Hum Genet
, vol.72
, pp. 58-62
-
-
Fitzgerald, P.H.1
Archer, S.A.2
Morris, C.M.3
-
4
-
-
0023933769
-
Parental centromere separation sequence and aneuploidy of the offspring
-
Banjnóczky K., Méhes K. Parental centromere separation sequence and aneuploidy of the offspring. Hum Genet. 78:1988;286-288.
-
(1988)
Hum Genet
, vol.78
, pp. 286-288
-
-
Banjnóczky, K.1
Méhes, K.2
-
5
-
-
0027443083
-
"premature anaphase" in a couple with recurrent miscarriages
-
Banjnóczky K., Gardó S. "Premature anaphase" in a couple with recurrent miscarriages. Hum Genet. 92:1993;388-390.
-
(1993)
Hum Genet
, vol.92
, pp. 388-390
-
-
Banjnóczky, K.1
Gardó, S.2
-
6
-
-
0028832160
-
Premature centromere division: A possible manifestation of chromosome instability
-
Méhes K., Bühler E.M. Premature centromere division. a possible manifestation of chromosome instability Am J Med Genet. 56:1995;76-79.
-
(1995)
Am J Med Genet
, vol.56
, pp. 76-79
-
-
Méhes, K.1
Bühler, E.M.2
-
7
-
-
0001610224
-
Multiple endocrine neoplasia type 1
-
L.J. DeGroot. Philadelphia: Saunders
-
Thakker R.V. Multiple endocrine neoplasia type 1. DeGroot L.J. Endocrinology. 1995;2815-2831 Saunders, Philadelphia.
-
(1995)
Endocrinology
, pp. 2815-2831
-
-
Thakker, R.V.1
-
8
-
-
0030963446
-
Positional cloning of the gene for multiple endocrine neoplasia type 1
-
Chandrasekharappa S.C., Guru S.C., Manickam P., Olufemi S.-E., Collins F.S., Emmert-Buck M.R., Debelenko L.V., Zhuang Z., Lubensky I.A., Liotta L.A., Crabtree J.S., Wang Y., Roe B.A., Weisemann J., Boguski M.S., Agarwal S.K., Kester M.B., Kim Y.S., Heppner C., Dong Q., Spiegel A.M., Burns A.L., Marx S.J. Positional cloning of the gene for multiple endocrine neoplasia type 1. Science. 276:1997;404-407.
-
(1997)
Science
, vol.276
, 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
Debelenko, L.V.7
Zhuang, Z.8
Lubensky, I.A.9
Liotta, L.A.10
Crabtree, J.S.11
Wang, Y.12
Roe, B.A.13
Weisemann, J.14
Boguski, M.S.15
Agarwal, S.K.16
Kester, M.B.17
Kim, Y.S.18
Heppner, C.19
Dong, Q.20
Spiegel, A.M.21
Burns, A.L.22
Marx, S.J.23
more..
-
9
-
-
8544279953
-
Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states
-
Argarwal S.K., Kester M.B., Debelenko L.V., Heppner C., Emmert-Buck M.R., Skarulis M.C., Doppman J.L., Kim Y.S., Lubensky I.A., Zhuang Z., Green J.S., Guru S.C., Manickam P., Olufemi S.-E., Liotta A.L., Chandrasekharappa S.C., Collins F.S., Spiegel A.M., Burns A.L., Marx S.J. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum Mol Genet. 6:1997;1169-1175.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1169-1175
-
-
Argarwal, 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, A.L.15
Chandrasekharappa, S.C.16
Collins, F.S.17
Spiegel, A.M.18
Burns, A.L.19
Marx, S.J.20
more..
-
10
-
-
17344363260
-
Characterization of mutations in patients with multiple endocrine neoplasia type 1
-
Bassett J.H., Forbes S.A., Pannett A.A., Lloyd S.E., Christie P.T., Wooding C., Harding B., Besser G.M., Edwards C.R., Monson J.P., Sampson J., Wass J.A., Wheeler M.H., Thakker R.V. Characterization of mutations in patients with multiple endocrine neoplasia type 1. Am J Hum Genet. 62:1998;232-244.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 232-244
-
-
Bassett, J.H.1
Forbes, S.A.2
Pannett, A.A.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.12
Wheeler, M.H.13
Thakker, R.V.14
-
11
-
-
0020531162
-
Chromosomal breakage in multiple endocrine adenomatosis (types I and II)
-
Gustavson K.-H., Jansson R., Öberg K. Chromosomal breakage in multiple endocrine adenomatosis (types I and II). Clin Genet. 23:1983;143-149.
-
(1983)
Clin Genet
, vol.23
, pp. 143-149
-
-
Gustavson, K.-H.1
Jansson, R.2
Öberg, K.3
-
12
-
-
0025850979
-
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1
-
Scappaticci S., Maraschio P., Del Ciotto N., Fossati G.S., Zonta A., Fraccaro M. Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. Cancer Genet Cytogenet. 52:1991;85-92.
-
(1991)
Cancer Genet Cytogenet
, vol.52
, pp. 85-92
-
-
Scappaticci, S.1
Maraschio, P.2
Del Ciotto, N.3
Fossati, G.S.4
Zonta, A.5
Fraccaro, M.6
-
13
-
-
0028922623
-
Chromosomal instability in multiple endocrine neoplasia type 1: Cytogenetic evaluation with DEB test
-
Tomassetti P., Cometa G., Del Vecchio E., Baserga M., Faccioli P., Bosoni D., Paolucci G., Barbara L. Chromosomal instability in multiple endocrine neoplasia type 1. cytogenetic evaluation with DEB test Cancer Genet Cytogenet. 79:1995;123-126.
-
(1995)
Cancer Genet Cytogenet
, vol.79
, pp. 123-126
-
-
Tomassetti, P.1
Cometa, G.2
Del Vecchio, E.3
Baserga, M.4
Faccioli, P.5
Bosoni, D.6
Paolucci, G.7
Barbara, L.8
-
14
-
-
0029840847
-
Genetic screening in hereditary multiple endocrine neoplasia type 1: Absence of a founder effect among Japanese families
-
Sakurai A., Katai M., Itakura Y., Nakajima K., Baba K., Hashizume K. Genetic screening in hereditary multiple endocrine neoplasia type 1. absence of a founder effect among Japanese families Jpn J Cancer Res. 87:1996;985-994.
-
(1996)
Jpn J Cancer Res
, vol.87
, pp. 985-994
-
-
Sakurai, A.1
Katai, M.2
Itakura, Y.3
Nakajima, K.4
Baba, K.5
Hashizume, K.6
-
15
-
-
0031613729
-
Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1
-
Sakurai A., Shirahama S., Fujimori M., Katai M., Itakura Y., Kobayashi S., Amano J., Fukushima Y., Hashizume K. Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1. J Hum Genet. 43:1998;199-201.
-
(1998)
J Hum Genet
, vol.43
, pp. 199-201
-
-
Sakurai, A.1
Shirahama, S.2
Fujimori, M.3
Katai, M.4
Itakura, Y.5
Kobayashi, S.6
Amano, J.7
Fukushima, Y.8
Hashizume, K.9
-
16
-
-
0027359959
-
Cytogenetics of multiple endocrine neoplasia syndromes: III. Analysis of an insulinoma from a subject with MEN 1 by chromosome painting
-
Maraschio P., Pezzolo A., Brandi M.L., Cortinovis M., Dainotti E., Scappaticci S., Fraccaro M. Cytogenetics of multiple endocrine neoplasia syndromes. III. Analysis of an insulinoma from a subject with MEN 1 by chromosome painting Cancer Genet Cytogenet. 70:1993;68-70.
-
(1993)
Cancer Genet Cytogenet
, vol.70
, pp. 68-70
-
-
Maraschio, P.1
Pezzolo, A.2
Brandi, M.L.3
Cortinovis, M.4
Dainotti, E.5
Scappaticci, S.6
Fraccaro, M.7
-
17
-
-
0027985762
-
Chromosome analysis of nine endocrine neoplasms of the pancreas
-
Long P.P., Hruban R.H., Lo R., Yeo C.J., Morsberger L.A., Griffin C.A. Chromosome analysis of nine endocrine neoplasms of the pancreas. Cancer Genet Cytogenet. 77:1994;55-59.
-
(1994)
Cancer Genet Cytogenet
, vol.77
, pp. 55-59
-
-
Long, P.P.1
Hruban, R.H.2
Lo, R.3
Yeo, C.J.4
Morsberger, L.A.5
Griffin, C.A.6
-
18
-
-
0028802374
-
Genetic abnormalities in sporadic parathyroid adenomas: Loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus
-
Thompson D.B., Samowitz W.S., Odelberg S., Davis R.K., Szabo J., Heath H. III Genetic abnormalities in sporadic parathyroid adenomas. loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus J Clin Endocrinol Metab. 80:1995;3377-3380.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 3377-3380
-
-
Thompson, D.B.1
Samowitz, W.S.2
Odelberg, S.3
Davis, R.K.4
Szabo, J.5
Heath H. III6
-
19
-
-
0030755071
-
Somatic mutation of the MEN1 gene in parathyroid tumours
-
Heppner C., Kester M.B., Agarwal S.K., Debelenko L.V., Emmert-Buck M.R., Guru S.C., Manickam P., Olufemi S.-E., Skarulis M.C., Doppman J.L., Alexander R.H., Kim Y.S., Saggar S.K., Lubensky I.A., Zhuang Z., Liotta L.A., Chandrasekharappa S.C., Collins F.S., Speigel A.M., Burns A.L., Marx S.J. Somatic mutation of the MEN1 gene in parathyroid tumours. Nat Genet. 16:1997;375-378.
-
(1997)
Nat Genet
, vol.16
, 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
Manickam, P.7
Olufemi, S.-E.8
Skarulis, M.C.9
Doppman, J.L.10
Alexander, R.H.11
Kim, Y.S.12
Saggar, S.K.13
Lubensky, I.A.14
Zhuang, Z.15
Liotta, L.A.16
Chandrasekharappa, S.C.17
Collins, F.S.18
Speigel, A.M.19
Burns, A.L.20
Marx, S.J.21
more..
-
20
-
-
0030810185
-
Somatic mutation of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas
-
Zhuang Z., Vortmeyer A.O., Pack S., Huang S., Pham T.A., Wang C., Park W.-S., Agarwal S.K., Debelenko L.V., Kester M.B., Guru S.C., Manickam P., Olufemi S.-E., Yu F., Heppner C., Crabtree J.S., Skarulis M.C., Venzon D.J., Emmert-Buck M.R., Speigel A.M., Chandrasekharappa S.C., Collins F.S., Burns A.L., Marx S.J., Jensen R.T., Liotta L.A., Lubensky I.A. Somatic mutation of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas. Cancer Res. 57:1997;4682-4686.
-
(1997)
Cancer Res
, vol.57
, pp. 4682-4686
-
-
Zhuang, Z.1
Vortmeyer, A.O.2
Pack, S.3
Huang, S.4
Pham, T.A.5
Wang, C.6
Park, W.-S.7
Agarwal, S.K.8
Debelenko, L.V.9
Kester, M.B.10
Guru, S.C.11
Manickam, P.12
Olufemi, S.-E.13
Yu, F.14
Heppner, C.15
Crabtree, J.S.16
Skarulis, M.C.17
Venzon, D.J.18
Emmert-Buck, M.R.19
Speigel, A.M.20
Chandrasekharappa, S.C.21
Collins, F.S.22
Burns, A.L.23
Marx, S.J.24
Jensen, R.T.25
Liotta, L.A.26
Lubensky, I.A.27
more..
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