-
1
-
-
1842283931
-
Isolation and characterization of a steroid sulfatase cDNA clone: Genomic deletions in patients with X-chromosome-linked ichthyosis
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 4519-4523
-
-
Ballabio, A.1
Parenti, G.2
Carrozzo, R.3
Sebastio, G.4
Andria, G.5
Buckle, V.6
Fraser, N.7
Craig, I.8
Rocchi, M.9
Romeo, G.10
-
2
-
-
0029840316
-
FHIT, a putative tumor suppressor in humans, is a dinucleoside 5′,5″-P1,P3-triphosphate hydrolase
-
(1996)
Biochemistry
, vol.35
, pp. 11529-11535
-
-
Barnes, L.D.1
Garrison, P.N.2
Siprashvili, Z.3
Guranowski, A.4
Robinson, A.K.5
Ingram, S.W.6
Croce, C.M.7
Ohta, M.8
Huebner, K.9
-
4
-
-
0032815795
-
The canine copper toxicosis locus is not syntenic with ATP7B or ATX and maps to a region showing homology to human 2p21
-
(1999)
Mamm Genome
, vol.10
, pp. 753-756
-
-
Dagenais, S.L.1
Guevara-Fujita, M.2
Loechel, R.3
Burgess, A.C.4
Miller, D.E.5
Yuzbasiyan-Gurkan, V.6
Brewer, G.J.7
Glover, T.W.8
-
5
-
-
0031043860
-
Structure and expression of the human FHIT gene in normal and tumor cells
-
(1997)
Cancer Res
, vol.57
, pp. 504-512
-
-
Druck, T.1
Hadaczk, P.2
Fu, T.B.3
Ohta, M.4
Siprashvili, Z.5
Baffa, R.6
Negrini, M.7
Kastury, K.8
Veronese, M.L.9
Rosen, D.10
Rothstein, J.11
McCue, P.12
Cotticelli, M.G.13
Inoue, H.14
Croce, C.M.15
Huebner, K.16
-
6
-
-
0035853128
-
FHIT gene therapy prevents tumor development in Fhit-deficient mice
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 3346-3351
-
-
Dumon, K.R.1
Ishii, H.2
Fong, L.Y.3
Zanesi, N.4
Fidanza, V.5
Mancini, R.6
Vecchione, A.7
Baffa, R.8
Trapasso, F.9
During, M.J.10
Huebner, K.11
Croce, C.M.12
-
8
-
-
12944309911
-
Muir-Torre-like syndrome in FHIT-deficient mice
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 4742-4747
-
-
Fong, L.Y.1
Fidanza, V.2
Zanesi, N.3
Lock, L.F.4
Siracusa, L.D.5
Mancini, R.6
Siprashvili, Z.7
Ottey, M.8
Martin, S.E.9
Druck, T.10
McCue, P.A.11
Croce, C.M.12
Huebner, K.13
-
9
-
-
0033843150
-
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation
-
(2000)
Am J Hum Genet
, vol.67
, pp. 563-573
-
-
Fukami, M.1
Kirsch, S.2
Schiller, S.3
Richter, A.4
Benes, V.5
Franco, B.6
Muroya, K.7
Rao, E.8
Merker, S.9
Niesler, B.10
Ballabio, A.11
Ansorge, W.12
Ogata, T.13
Rappold, G.A.14
-
15
-
-
0026550844
-
Three distinct regions involved in 3p deletion in human lung cancer
-
(1992)
Oncogene
, vol.7
, pp. 445-449
-
-
Hibi, K.1
Takahashi, T.2
Yamakawa, K.3
Ueda, R.4
Sekido, Y.5
Atiyoshi, Y.6
Suyama, M.7
Takagi, H.8
Nakamura, Y.9
Takahashi, T.10
-
17
-
-
0032889647
-
Frequent deletions within FRA7G at 7q31.2 in invasive epithelial ovarian cancer
-
(1999)
Genes Chromosomes Cancer
, vol.24
, pp. 48-55
-
-
Huang, H.1
Reed, C.P.2
Mordi, A.3
Lomberk, G.4
Wang, L.5
Shridhar, V.6
Hartmann, L.7
Jenkins, R.8
Smith, D.I.9
-
20
-
-
0033978639
-
A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins
-
(2000)
Hum Mol Genet
, vol.9
, pp. 311-319
-
-
Lahn, B.T.1
Page, D.C.2
-
24
-
-
0034654641
-
Chromosomal fragile site FRA16D and DNA instability in cancer
-
(2000)
Cancer Res
, vol.60
, pp. 1683-1689
-
-
Mangelsdorf, M.1
Ried, K.2
Woollatt, E.3
Dayan, S.4
Eyre, H.5
Finnis, M.6
Hobson, L.7
Nancarrow, J.8
Venter, D.9
Baker, E.10
Richards, R.I.11
-
26
-
-
13144283613
-
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 8141-8146
-
-
Mishmar, D.1
Rahat, A.2
Scherer, S.W.3
Nyakatura, G.4
Hinzmann, B.5
Kohwi, Y.6
Mandel-Gutfroind, Y.7
Lee, J.R.8
Drescher, B.9
Sas, D.E.10
Margalit, H.11
Platzer, M.12
Weiss, A.13
Tsui, L.C.14
Rosenthal, A.15
Kerem, B.16
-
28
-
-
0029902071
-
The FHIT gene at 3p14.2 is abnormal in breast carcinomas
-
(1996)
Cancer Res
, vol.56
, pp. 3173-3179
-
-
Negrini, M.1
Monaco, C.2
Vorechovsky, I.3
Ohta, M.4
Druck, T.5
Baffa, R.6
Huebner, K.7
Croce, C.M.8
-
29
-
-
13344279424
-
The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers
-
(1996)
Cell
, vol.84
, pp. 587-597
-
-
Ohta, M.1
Inoue, H.2
Cotticelli, M.G.3
Kastury, K.4
Baffa, R.5
Palazzo, J.6
Siprashvili, Z.7
Mori, M.8
McCue, P.9
Druck, T.10
-
30
-
-
0032542701
-
Protein expression and functional analysis of the FHIT gene in human tumor cells
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 426-432
-
-
Otterson, G.A.1
Xiao, G.H.2
Geradts, J.3
Jin, F.4
Chen, W.5
Niklinska, W.6
Kaye, F.J.7
Yeung, R.S.8
-
31
-
-
17444440946
-
Common chromosomal fragile site FRA16D sequence: Identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1651-1663
-
-
Ried, K.1
Finnis, M.2
Hobson, L.3
Mangelsdorf, M.4
Dayan, S.5
Nancarrow, J.K.6
Woollatt, E.7
Kremmidiotis, G.8
Gardner, A.9
Venter, D.10
Baker, E.11
Richards, R.I.12
-
33
-
-
13144262880
-
Replacement of FHIT in cancer cells suppresses tumorigenicity
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 13771-13776
-
-
Siprashvili, Z.1
Sozzi, G.2
Barnes, L.D.3
McCue, P.4
Robinson, A.K.5
Eryomin, V.6
Sard, L.7
Tagliabue, E.8
Greco, A.9
Fusetti, L.10
Schwartz, G.11
Pierotti, M.A.12
Croce, C.M.13
Huebner, K.14
-
35
-
-
15844384990
-
The FHIT gene 3p14.2 is abnormal in lung cancer
-
(1996)
Cell
, vol.85
, pp. 17-26
-
-
Sozzi, G.1
Veronese, M.L.2
Negrini, M.3
Baffa, R.4
Cotticelli, M.G.5
Inoue, H.6
Tornielli, S.7
Pilotti, S.8
De Gregorio, L.9
Pastorino, U.10
Pierotti, M.A.11
Ohta, M.12
Huebner, K.13
Croce, C.M.14
-
39
-
-
0024208474
-
The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolution
-
(1988)
Cell
, vol.55
, pp. 1123-1135
-
-
Yen, P.H.1
Marsh, B.2
Allen, E.3
Tsai, S.P.4
Ellison, J.5
Connolly, L.6
Neiswanger, K.7
Shapiro, L.J.8
|