-
1
-
-
2442589606
-
Loss of WWOX expression in gastric carcinoma
-
Aqeilan RI, Kuroki T, Pekarsky Y, Albagha O, Trapasso F, et al: Loss of WWOX expression in gastric carcinoma. Clin Cancer Res 10:3053-3058 (2004).
-
(2004)
Clin Cancer Res
, vol.10
, pp. 3053-3058
-
-
Aqeilan, R.I.1
Kuroki, T.2
Pekarsky, Y.3
Albagha, O.4
Trapasso, F.5
-
2
-
-
0036131979
-
Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells
-
Arlt MF, Miller DE, Beer DG, Glover TW: Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells. Genes Chromosomes Cancer 33:82-92 (2002).
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 82-92
-
-
Arlt, M.F.1
Miller, D.E.2
Beer, D.G.3
Glover, T.W.4
-
5
-
-
22244468667
-
Loss of FHIT expression in breast cancer is correlated with poor prognostic markers
-
Arun B, Kilic G, Yen C, Foster B, Yardley DA, et al: Loss of FHIT expression in breast cancer is correlated with poor prognostic markers. Cancer Epidemiol Biomarkers Prev 14:1681-1685 (2005).
-
(2005)
Cancer Epidemiol Biomarkers Prev
, vol.14
, pp. 1681-1685
-
-
Arun, B.1
Kilic, G.2
Yen, C.3
Foster, B.4
Yardley, D.A.5
-
6
-
-
0030584084
-
Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro
-
Baumann P, Benson FE, West SC: Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro. Cell 87:757-766 (1996).
-
(1996)
Cell
, vol.87
, pp. 757-766
-
-
Baumann, P.1
Benson, F.E.2
West, S.C.3
-
7
-
-
0037069944
-
Evidence that instability within the FRA3B region extends four megabases
-
Becker NA, Thorland EC, Denison SR, Phillips LA, Smith DI: Evidence that instability within the FRA3B region extends four megabases. Oncogene 21:8713-8722 (2002).
-
(2002)
Oncogene
, vol.21
, pp. 8713-8722
-
-
Becker, N.A.1
Thorland, E.C.2
Denison, S.R.3
Phillips, L.A.4
Smith, D.I.5
-
8
-
-
0034655131
-
WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.2-24.1, a region frequently affected in breast cancer
-
Bednarek AK, Laflin KJ, Daniel RL, Liao Q, Hawkins KA, Aldaz CM: WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.2-24.1, a region frequently affected in breast cancer. Cancer Res 60:2140-2145 (2000).
-
(2000)
Cancer Res
, vol.60
, pp. 2140-2145
-
-
Bednarek, A.K.1
Laflin, K.J.2
Daniel, R.L.3
Liao, Q.4
Hawkins, K.A.5
Aldaz, C.M.6
-
9
-
-
33644794329
-
Human retinoic acid receptor-related orphan receptor alpha1 overexpression protects neurons against oxidative stress-induced apoptosis
-
Boukhtouche F, Vodjdani G, Jarvis CL, Bakouche J, Staels B, et al: Human retinoic acid receptor-related orphan receptor alpha1 overexpression protects neurons against oxidative stress-induced apoptosis. J Neurochem 96:1778-1789 (2006).
-
(2006)
J Neurochem
, vol.96
, pp. 1778-1789
-
-
Boukhtouche, F.1
Vodjdani, G.2
Jarvis, C.L.3
Bakouche, J.4
Staels, B.5
-
10
-
-
0038732456
-
Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27
-
Cesari R, Martin ES, Calin GA, Pentimalli F, Bichi R, et al: Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27. Proc Natl Acad Sci USA 100:5956-5961 (2003).
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 5956-5961
-
-
Cesari, R.1
Martin, E.S.2
Calin, G.A.3
Pentimalli, F.4
Bichi, R.5
-
11
-
-
0042522482
-
Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer
-
Denison SF, Callahan G, Becker NA, Phillips LA, Smith DI: Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer. Genes Chromosomes Cancer 38:40-52 (2003).
-
(2003)
Genes Chromosomes Cancer
, vol.38
, pp. 40-52
-
-
Denison, S.F.1
Callahan, G.2
Becker, N.A.3
Phillips, L.A.4
Smith, D.I.5
-
12
-
-
33747195058
-
Trends in brain cancer incidence and survival in the United States: Surveillance, epidemiology, and end results program. 1973 to 2001
-
Deorah S, Lynch CF, Bibenaller ZA, Ryken TC: Trends in brain cancer incidence and survival in the United States: Surveillance, epidemiology, and end results program. 1973 to 2001. Neurosurg Focus 20:E1 (2006).
-
(2006)
Neurosurg Focus
, vol.20
-
-
Deorah, S.1
Lynch, C.F.2
Bibenaller, Z.A.3
Ryken, T.C.4
-
13
-
-
0031043860
-
Structure and expression of the human FHIT gene in normal and tumor cells
-
Druck T, Hadaczek P, Fu TB, Ohta M, Siprashvili Z, et al: Structure and expression of the human FHIT gene in normal and tumor cells. Cancer Res 57:504-512 (1997).
-
(1997)
Cancer Res
, vol.57
, pp. 504-512
-
-
Druck, T.1
Hadaczek, P.2
Fu, T.B.3
Ohta, M.4
Siprashvili, Z.5
-
14
-
-
0035853128
-
FHIT gene therapy prevents tumor development in Fhit-deficient mice
-
Dumon KR, Ishii H, Fong LY, Zanesi N, Pidanza V, et al: FHIT gene therapy prevents tumor development in Fhit-deficient mice. Proc Natl Acad Sci USA 98:3346-3351 (2001).
-
(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
Pidanza, V.5
-
15
-
-
0031907862
-
Orphan nuclear receptor ROR alpha-deficient mice display the cerebellar defects of staggerer
-
Dussaulat I, Fawcett D, Matthyssen A, Bader JA, Giguere V: Orphan nuclear receptor ROR alpha-deficient mice display the cerebellar defects of staggerer. Mech Dev 70:147-153 (1990).
-
(1990)
Mech Dev
, vol.70
, pp. 147-153
-
-
Dussaulat, I.1
Fawcett, D.2
Matthyssen, A.3
Bader, J.A.4
Giguere, V.5
-
16
-
-
0031758918
-
Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers
-
Engelman JA, Zhang XL, Lisanti MP: Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers. FEBS Lett 436:403-410 (1998).
-
(1998)
FEBS Lett
, vol.436
, pp. 403-410
-
-
Engelman, J.A.1
Zhang, X.L.2
Lisanti, M.P.3
-
17
-
-
27344455410
-
WWOX gene restoration prevents lung cancer growth in vitro and in vivo
-
Fabbri M, Iliopoulos D, Traposso F, Aqeilan RI, Cimmino A, et al: WWOX gene restoration prevents lung cancer growth in vitro and in vivo. Proc Natl Acad Sci USA 102:15611-15616 (2005).
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 15611-15616
-
-
Fabbri, M.1
Iliopoulos, D.2
Traposso, F.3
Aqeilan, R.I.4
Cimmino, A.5
-
18
-
-
0025056930
-
Identification of a chromosome 18q gene that is altered in colorectal cancers
-
Fearon ER, Cho KR, Nigro JM, Kern SE, Simons JW, et al: Identification of a chromosome 18q gene that is altered in colorectal cancers. Science 247:49-56 (1990).
-
(1990)
Science
, vol.247
, pp. 49-56
-
-
Fearon, E.R.1
Cho, K.R.2
Nigro, J.M.3
Kern, S.E.4
Simons, J.W.5
-
19
-
-
0242720711
-
Preferential integration of human papillomavirus type 18 near the c-Myc locus in cervical carcinoma
-
Ferber MJ, Thorland EC, Brink AA, Rapp AK, Phillips LA, et al: Preferential integration of human papillomavirus type 18 near the c-Myc locus in cervical carcinoma. Oncogene 22:7233-7242 (2003).
-
(2003)
Oncogene
, vol.22
, pp. 7233-7242
-
-
Ferber, M.J.1
Thorland, E.C.2
Brink, A.A.3
Rapp, A.K.4
Phillips, L.A.5
-
20
-
-
17844399776
-
Patient tumor EGFR and PDGFRA gene amplifications retained in an invasive intracranial xenograft model of glioblastoma multiforme
-
Giannini C, Sarkaria JN, Saito A, Uhm JH, Galanis E, et al: Patient tumor EGFR and PDGFRA gene amplifications retained in an invasive intracranial xenograft model of glioblastoma multiforme. Neuro Oncol 7:164-176 (2005).
-
(2005)
Neuro Oncol
, vol.7
, pp. 164-176
-
-
Giannini, C.1
Sarkaria, J.N.2
Saito, A.3
Uhm, J.H.4
Galanis, E.5
-
21
-
-
10744220604
-
Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer
-
Ginestier C, Bardou VJ, Popvici C, Charafe-Jauffret E, Bertucci F, et al: Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer. Int J Cancer 107:854-862 (2003).
-
(2003)
Int J Cancer
, vol.107
, pp. 854-862
-
-
Ginestier, C.1
Bardou, V.J.2
Popvici, C.3
Charafe-Jauffret, E.4
Bertucci, F.5
-
22
-
-
0021278143
-
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
-
Glover TW, Berger C, Coyle J, Echo B: DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:136-145 (1984).
-
(1984)
Hum Genet
, vol.67
, pp. 136-145
-
-
Glover, T.W.1
Berger, C.2
Coyle, J.3
Echo, B.4
-
23
-
-
0344002715
-
Fhit expression is absent or reduced in a subset of primary head and neck cancer
-
Gotte K, Hadaczek P, Coy JF, Wirtz HW, Riedel F, et al: Fhit expression is absent or reduced in a subset of primary head and neck cancer. Anticancer Res 20:1057-1060 (2000).
-
(2000)
Anticancer Res
, vol.20
, pp. 1057-1060
-
-
Gotte, K.1
Hadaczek, P.2
Coy, J.F.3
Wirtz, H.W.4
Riedel, F.5
-
24
-
-
1842581808
-
The fragile genes FHIT and WWOX are inactivated coordinately in invasive breast carcinoma
-
Guler G, Uner A, Guler N, Han SY, Iliopoulos D, et al: The fragile genes FHIT and WWOX are inactivated coordinately in invasive breast carcinoma. Cancer 100:1605-1614 (2004).
-
(2004)
Cancer
, vol.100
, pp. 1605-1614
-
-
Guler, G.1
Uner, A.2
Guler, N.3
Han, S.Y.4
Iliopoulos, D.5
-
25
-
-
0032527899
-
Absence of reduction of Fhit expression in most clear cell renal carcinomas
-
Hadaczek P, Siprashvili Z, Markiewski M, Domagala W, Druck T, et al: Absence of reduction of Fhit expression in most clear cell renal carcinomas. Cancer Res 58:2946-2951 (1998).
-
(1998)
Cancer Res
, vol.58
, pp. 2946-2951
-
-
Hadaczek, P.1
Siprashvili, Z.2
Markiewski, M.3
Domagala, W.4
Druck, T.5
-
26
-
-
33845424480
-
Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C 1-relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints
-
Helmrich A, Stout-Weider K, Matthaei A, Hermann K, Heiden T, Schrock E: Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C 1-relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints. Int J Cancer 120:48-54 (2007).
-
(2007)
Int J Cancer
, vol.120
, pp. 48-54
-
-
Helmrich, A.1
Stout-Weider, K.2
Matthaei, A.3
Hermann, K.4
Heiden, T.5
Schrock, E.6
-
27
-
-
33845625674
-
FRA1E common fragile site breaks map within a 370 kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD)
-
Hormozian F, Schmitt JG, Sagulenko E, Schwab M, Savelyeva L: FRA1E common fragile site breaks map within a 370 kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD). Cancer Lett 246:82-91 (2007).
-
(2007)
Cancer Lett
, vol.246
, pp. 82-91
-
-
Hormozian, F.1
Schmitt, J.G.2
Sagulenko, E.3
Schwab, M.4
Savelyeva, L.5
-
28
-
-
30144438249
-
Roles of FHIT and WWOX fragile genes in cancer
-
Iliopoulos D, Guler G, Han SY, Druck T, Ottey M, et al: Roles of FHIT and WWOX fragile genes in cancer. Cancer Lett 232:27-36 (2006).
-
(2006)
Cancer Lett
, vol.232
, pp. 27-36
-
-
Iliopoulos, D.1
Guler, G.2
Han, S.Y.3
Druck, T.4
Ottey, M.5
-
29
-
-
0034102258
-
Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation
-
Jin H, Gardner RJ, Viswesvaraiah R, Muntoni F, Roberts RG: Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation. Eur J Hum Genet 8:87-94 (2000).
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 87-94
-
-
Jin, H.1
Gardner, R.J.2
Viswesvaraiah, R.3
Muntoni, F.4
Roberts, R.G.5
-
30
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, et al: Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392:605-608 (1998).
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
-
31
-
-
0023614271
-
Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
-
Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, Feener C, Kunkel LM: Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50:509-517 (1987).
-
(1987)
Cell
, vol.50
, pp. 509-517
-
-
Koenig, M.1
Hoffman, E.P.2
Bertelson, C.J.3
Monaco, A.P.4
Feener, C.5
Kunkel, L.M.6
-
32
-
-
0034306548
-
The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations
-
Krummel KA, Roberts LR, Kawakami M, Glover TW, Smith DI: The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations. Genomics 69:37-46 (2000).
-
(2000)
Genomics
, vol.69
, pp. 37-46
-
-
Krummel, K.A.1
Roberts, L.R.2
Kawakami, M.3
Glover, T.W.4
Smith, D.I.5
-
33
-
-
0032524625
-
Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher
-
Lalouette A, Guenet JL, Vriz S: Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher. Genomics 50:9-13 (1998).
-
(1998)
Genomics
, vol.50
, pp. 9-13
-
-
Lalouette, A.1
Guenet, J.L.2
Vriz, S.3
-
34
-
-
36248991908
-
Non-random inactivation of large common fragile site genes in different cancers
-
McAvoy S. Ganapathiraju SC, Ducharme-Smith AL, Pritchett JR, Kosari F, et al: Non-random inactivation of large common fragile site genes in different cancers. Cytogenet Genome Res 118:260-269 (2007).
-
(2007)
Cytogenet Genome Res
, vol.118
, pp. 260-269
-
-
McAvoy, S.1
Ganapathiraju, S.C.2
Ducharme-Smith, A.L.3
Pritchett, J.R.4
Kosari, F.5
-
35
-
-
13144283613
-
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site
-
Mishmar D, Rahat A, Scherer SW, Nyakatura G, Hinzmann B, et al: Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proc Natl Acad Sci USA 95:2311-2319 (1998).
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 2311-2319
-
-
Mishmar, D.1
Rahat, A.2
Scherer, S.W.3
Nyakatura, G.4
Hinzmann, B.5
-
36
-
-
0035949591
-
WWOX: A candidate tumor suppressor gene involved in multiple tumor types
-
Paige AJ, Taylor KJ, Taylor C, Hillier SG, Farrington S, et al: WWOX: a candidate tumor suppressor gene involved in multiple tumor types. Proc Natl Acad Sci USA 98:11417-11422 (2001).
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 11417-11422
-
-
Paige, A.J.1
Taylor, K.J.2
Taylor, C.3
Hillier, S.G.4
Farrington, S.5
-
37
-
-
4344715921
-
Frequent downregulation and loss of WWOX gene expression in human hepatocellular carcinoma
-
Park SW, Ludes-Meyers J, Zimonjic DB, Durkin ME, Popescu NC, Aldaz CM: Frequent downregulation and loss of WWOX gene expression in human hepatocellular carcinoma. Br J Cancer 91:753-759 (2004).
-
(2004)
Br J Cancer
, vol.91
, pp. 753-759
-
-
Park, S.W.1
Ludes-Meyers, J.2
Zimonjic, D.B.3
Durkin, M.E.4
Popescu, N.C.5
Aldaz, C.M.6
-
38
-
-
32944460958
-
WWOX - the FRA16D cancer gene: Expression correlation with breast cancer progression and prognosis
-
Pluciennik E, Kusinska R, Potemski P, Kubiak R, Kordek R, Bednarek AK: WWOX - the FRA16D cancer gene: expression correlation with breast cancer progression and prognosis. Eur J Surg Oncol 32:153-157 (2006).
-
(2006)
Eur J Surg Oncol
, vol.32
, pp. 153-157
-
-
Pluciennik, E.1
Kusinska, R.2
Potemski, P.3
Kubiak, R.4
Kordek, R.5
Bednarek, A.K.6
-
39
-
-
39049128328
-
WWOX, a chromosomal fragile site gene and its role in cancer
-
Ramos D, Aldaz CM: WWOX, a chromosomal fragile site gene and its role in cancer. Adv Exp Med Biol 587:149-159 (2006).
-
(2006)
Adv Exp Med Biol
, vol.587
, pp. 149-159
-
-
Ramos, D.1
Aldaz, C.M.2
-
40
-
-
4644319208
-
Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: Possible association with an inherited disease and cancer
-
Rozier L, El-Achkar E, Apiou F, Debatisse M: Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer. Oncogene 23:6872-6880 (2004).
-
(2004)
Oncogene
, vol.23
, pp. 6872-6880
-
-
Rozier, L.1
El-Achkar, E.2
Apiou, F.3
Debatisse, M.4
-
42
-
-
33344454749
-
The role of dystrophin in the central nervous system: A mini review
-
Sekiguchi M: The role of dystrophin in the central nervous system: a mini review. Acta Myol 24:93-97 (2005).
-
(2005)
Acta Myol
, vol.24
, pp. 93-97
-
-
Sekiguchi, M.1
-
43
-
-
0027325816
-
Cloning of human, mouse and fission yeast recombination genes homolgous to RAD51 and recA
-
Shinohara A, Ogawa H, Matsuda Y, Ushio N, Ikeo K, Ogawa T: Cloning of human, mouse and fission yeast recombination genes homolgous to RAD51 and recA. Nat Genet 4:239-243 (1993).
-
(1993)
Nat Genet
, vol.4
, pp. 239-243
-
-
Shinohara, A.1
Ogawa, H.2
Matsuda, Y.3
Ushio, N.4
Ikeo, K.5
Ogawa, T.6
-
44
-
-
13144262880
-
Replacement of Fhit in cancer cells suppresses tumorigenicity
-
Siprashvili Z, Sozzi G, Barnes LD, McCue P, Robinson AK, et al: Replacement of Fhit in cancer cells suppresses tumorigenicity. Proc Natl Acad Sci USA 94:13771-13776 (1997).
-
(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
-
45
-
-
0031963434
-
Common fragile sites and cancer (review)
-
Smith DI, Huang H, Wang L: Common fragile sites and cancer (review). Int J Oncol 12:187-196 (1998).
-
(1998)
Int J Oncol
, vol.12
, pp. 187-196
-
-
Smith, D.I.1
Huang, H.2
Wang, L.3
-
46
-
-
30144442771
-
Common fragile sites, extremely large genes, neural development and cancer
-
Smith DI, Zhu Y, McAvoy S, Kuhn R: Common fragile sites, extremely large genes, neural development and cancer. Cancer Lett 232:48-57 (2006).
-
(2006)
Cancer Lett
, vol.232
, pp. 48-57
-
-
Smith, D.I.1
Zhu, Y.2
McAvoy, S.3
Kuhn, R.4
-
47
-
-
15844384990
-
The FHIT gene 3p14.2 is abnormal in lung cancer
-
Sozzi G, Veronese ML, Negrini M, Baffa R, Cotticelli MG, et al: The FHIT gene 3p14.2 is abnormal in lung cancer. Cell 85:17-26 (1996).
-
(1996)
Cell
, vol.85
, pp. 17-26
-
-
Sozzi, G.1
Veronese, M.L.2
Negrini, M.3
Baffa, R.4
Cotticelli, M.G.5
-
49
-
-
0033810575
-
The clinical significance of fragile sites on human chromosomes
-
Sutherland GR, Baker E: The clinical significance of fragile sites on human chromosomes. Clin Genet 58:157-161 (2000).
-
(2000)
Clin Genet
, vol.58
, pp. 157-161
-
-
Sutherland, G.R.1
Baker, E.2
-
50
-
-
0029061046
-
The molecular basis of fragile sites in human chromosomes
-
Sutherland GR, Richards RI: The molecular basis of fragile sites in human chromosomes. Curr Opin Genet Dev 5:323-327 (1995a).
-
(1995)
Curr Opin Genet Dev
, vol.5
, pp. 323-327
-
-
Sutherland, G.R.1
Richards, R.I.2
-
51
-
-
0028997643
-
Simple tandem DNA repeats and human genetic disease
-
Sutherland GR, Richards RI: Simple tandem DNA repeats and human genetic disease. Proc Natl Acad Sci USA 92:3636-3641 (1995b).
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3636-3641
-
-
Sutherland, G.R.1
Richards, R.I.2
-
52
-
-
33644863950
-
A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family
-
Tabolacci E, Pomponi MG, Pietrobono R, Terracciano A, Chiurazzi P, Neri G: A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family. Am J Med Genet A 140:482-487 (2006).
-
(2006)
Am J Med Genet A
, vol.140
, pp. 482-487
-
-
Tabolacci, E.1
Pomponi, M.G.2
Pietrobono, R.3
Terracciano, A.4
Chiurazzi, P.5
Neri, G.6
-
53
-
-
0038278610
-
Tourette Syndrome Association International Consortium for Genetics: CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder
-
Verkerk AJ, Mathews CA, Hoose M, Eussen BH, Heutink P, Oostra BA: Tourette Syndrome Association International Consortium for Genetics: CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics 82:1-9 (2003).
-
(2003)
Genomics
, vol.82
, pp. 1-9
-
-
Verkerk, A.J.1
Mathews, C.A.2
Hoose, M.3
Eussen, B.H.4
Heutink, P.5
Oostra, B.A.6
-
54
-
-
0037327040
-
A complex deletion-inversion event results in a chimeric IL1RAPL1-dystrophin transcript and a contiguous gene deletion syndrome
-
Wheway JM, Yau SC, Nihalani V, Ellis D, Irving M, et al: A complex deletion-inversion event results in a chimeric IL1RAPL1-dystrophin transcript and a contiguous gene deletion syndrome. J Med Genet 40:127-131 (2003).
-
(2003)
J Med Genet
, vol.40
, pp. 127-131
-
-
Wheway, J.M.1
Yau, S.C.2
Nihalani, V.3
Ellis, D.4
Irving, M.5
-
55
-
-
16644384244
-
IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric of DAX1
-
Zhang YH, Huang BL, Niakan KK, McCabe LL, McCabe ER, Dipple KM: IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric of DAX1. Hum Mutat 24:273 (2004).
-
(2004)
Hum Mutat
, vol.24
, pp. 273
-
-
Zhang, Y.H.1
Huang, B.L.2
Niakan, K.K.3
McCabe, L.L.4
McCabe, E.R.5
Dipple, K.M.6
-
56
-
-
33749188577
-
Aberrant FHIT protein expression in classical Hodgkin's lymphoma: A potential marker
-
Zhao P, Lam AK, Lu YL, Zhong M, Chen LH, Pu XL: Aberrant FHIT protein expression in classical Hodgkin's lymphoma: a potential marker. Pathology 38:399-402 (2006).
-
(2006)
Pathology
, vol.38
, pp. 399-402
-
-
Zhao, P.1
Lam, A.K.2
Lu, Y.L.3
Zhong, M.4
Chen, L.H.5
Pu, X.L.6
-
57
-
-
33646706084
-
RORA, a large common fragile site gene, is involved in cellular stress response
-
Zhu Y, McAvoy S, Kuhn R, Smith DI: RORA, a large common fragile site gene, is involved in cellular stress response. Oncogene 25:2901-2908 (2006).
-
(2006)
Oncogene
, vol.25
, pp. 2901-2908
-
-
Zhu, Y.1
McAvoy, S.2
Kuhn, R.3
Smith, D.I.4
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