-
2
-
-
0032510597
-
GFRalpha3 is an orphan member of the GDNF/neurturin/persephin receptor family
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 5801-5806
-
-
Baloh, R.H.1
Gorodinsky, A.2
Golden, J.P.3
Tansey, M.G.4
Keck, C.L.5
Popescu, N.C.6
Johnson, E.M.7
Milbrandt, J.8
-
3
-
-
0032400972
-
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31
-
(1998)
Genomics
, vol.54
, pp. 250-255
-
-
Bartoloni, L.1
Horrigan, S.K.2
Viles, K.D.3
Gilchrist, J.M.4
Stajich, J.M.5
Vance, J.M.6
Yamaoka, L.H.7
Pericak-Vance, M.A.8
Westbrook, C.A.9
Speer, M.C.10
-
9
-
-
85001626364
-
Gene mapping by FISH
-
"Methods in Molecular Biology" (J. Boultwood, Ed.) Humana Press, Totowa, NJ
-
(1996)
, vol.68
, pp. 53-76
-
-
Espinosa, R.1
Le Beau, M.M.2
-
11
-
-
0030662273
-
Human cancer syndromes: Clues to the origin and nature of cancer
-
(1999)
Science
, vol.278
, pp. 1043-1050
-
-
Fearon, E.R.1
-
12
-
-
0028581973
-
A highly conserved eukaryotic protein family possessing properties of polypeptide chain release factor
-
(1994)
Nature
, vol.372
, pp. 701-703
-
-
Frolova, L.1
Le Goff, X.2
Rasmussen, H.H.3
Cheperegin, S.4
Drugeon, G.5
Kress, M.6
Arman, I.7
Haenni, A.L.8
Celis, J.E.9
Philippe, M.10
Justesen, J.11
Kisselev, L.12
-
16
-
-
0032987868
-
Human release factor eRF1: Structural organization of the unique functional gene on chromosome 5 and of the three processed pseudogenes
-
(1999)
FEBS Lett.
, vol.454
, pp. 131-136
-
-
Guenet, L.1
Toutain, B.2
Guilleret, I.3
Chauvel, B.4
Deaven, L.L.5
Longmire, J.L.6
Le Gall, J.Y.7
David, V.8
Le Treut, A.9
-
17
-
-
0343619383
-
Identification and characterization of a novel polycystin family member, polycystin-L2, in mouse and human: Sequence, expression, alternative splicing, and chromosomal localization
-
(2000)
Genomics
, vol.64
, pp. 241-251
-
-
Guo, L.1
Schreiber, T.H.2
Weremowicz, S.3
Morton, C.C.4
Lee, C.5
Zhou, J.6
-
18
-
-
0033118872
-
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequences
-
(1999)
Genomics
, vol.57
, pp. 24-35
-
-
Horrigan, S.K.1
Bartoloni, L.2
Speer, M.C.3
Fulton, N.4
Kravarusic, J.5
Ramesar, R.6
Vance, J.M.7
Yamaoka, L.H.8
Westbrook, C.A.9
-
19
-
-
0034177514
-
Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31
-
(2000)
Blood
, vol.95
, pp. 2372-2377
-
-
Horrigan, S.K.1
Arbieva, Z.H.2
Xie, H.Y.3
Kravarusic, J.4
Fulton, N.C.5
Naik, H.6
Le, T.T.7
Westbrook, C.A.8
-
20
-
-
0031745208
-
Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 251-256
-
-
Jaju, R.J.1
Boultwood, J.2
Oliver, F.J.3
Kostrzewa, M.4
Fidler, C.5
Parker, N.6
McPherson, J.D.7
Morris, S.W.8
Muller, U.9
Wainscoat, J.S.10
Kearney, L.11
-
21
-
-
0034595235
-
cDNA cloning, expression pattern, genomic structure, and chromosomal location of RAB6KIFL, a human kinesin-like gene
-
(2000)
Gene
, vol.248
, pp. 117-125
-
-
Lai, F.1
Fernald, A.A.2
Zhao, N.3
Le Beau, M.M.4
-
23
-
-
0034658548
-
Molecular characterization of KLHL3, a human homologue of the Drosophila kelch gene
-
(2000)
Genomics
, vol.66
, pp. 65-75
-
-
Lai, F.1
Orelli, B.J.2
Till, B.G.3
Godley, L.A.4
Fernald, A.A.5
Pamintuan, L.6
Le Beau, M.M.7
-
24
-
-
0022617302
-
Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: Further evidence for characteristic abnormalities of chromosomes no. 5 and 7
-
(1986)
J. Clin. Oncol.
, vol.4
, pp. 325-345
-
-
Le Beau, M.M.1
Albain, K.S.2
Larson, R.A.3
Vardiman, J.W.4
Davis, E.M.5
Blough, R.R.6
Golomb, H.M.7
Rowley, J.D.8
-
25
-
-
0027315865
-
Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant diseases
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 5484-5488
-
-
Le Beau, M.M.1
Espinosa, R.E.2
Neuman, W.L.3
Stock, W.4
Roulston, D.5
Larson, R.A.6
Keinanen, M.7
Westbrook, C.A.8
-
26
-
-
0032805321
-
Spectral karyotyping study of the HL-60 cell line: Detection of complex rearrangements involving chromosomes 5, 7, and 16 and delineation of critical region of deletion on 5q31.1
-
(1999)
Cancer Genet. Cytogenet.
, vol.113
, pp. 105-109
-
-
Liang, J.C.1
Ning, Y.2
Wang, R.-Y.3
Padilla-Nash, H.M.4
Schröck, E.5
Soenksen, D.6
Nagarajan, L.7
Ried, T.8
-
29
-
-
0032434324
-
A new human nm23 homologue (nm23-H5) specifically expressed in testis germinal cells
-
(1998)
FEBS Lett.
, vol.434
, pp. 289-294
-
-
Munier, A.1
Feral, C.2
Milon, L.3
Pinon, V.P.4
Gyapay, G.5
Capeau, J.6
Guellaen, G.7
Lacombe, M.L.8
-
30
-
-
0029284338
-
Isolation and characterization of a novel, low abundant hnRNP protein: A0
-
(1995)
RNA
, vol.1
, pp. 171-182
-
-
Myer, V.E.1
Steitz, J.A.2
-
33
-
-
0032816182
-
Characterization of Mayven, a novel actin-binding protein predominantly expressed in brain
-
(1999)
Mol. Biol. Cell
, vol.10
, pp. 2361-2375
-
-
Soltysik-Espanola, M.1
Rogers, R.A.2
Jiang, S.3
Kim, T.A.4
Gaedigk, R.5
White, R.A.6
Avraham, H.7
Avraham, S.8
-
34
-
-
0032830638
-
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myeloid leukemia
-
(1999)
Nat. Genet.
, vol.23
, pp. 166-175
-
-
Song, W.J.1
Sullivan, M.G.2
Legare, R.D.3
Hutchings, S.4
Tan, X.5
Kufrin, D.6
Ratajczak, J.7
Resende, I.C.8
Haworth, C.9
Hock, R.10
Loh, M.11
Felix, C.12
Roy, D.C.13
Busque, L.14
Kurnit, D.15
Willman, C.16
Gewirtz, A.M.17
Speck, N.A.18
Bushweller, J.H.19
Li, F.P.20
Gardiner, K.21
Poncz, M.22
Maris, J.M.23
Gilliland, D.G.24
more..
-
36
-
-
0024281381
-
A zinc finger-encoding gene coregulated with c-fos during growth and differentiation, and after cellular depolarization
-
(1988)
Cell
, vol.53
, pp. 37-43
-
-
Sukhatme, V.P.1
Cao, X.M.2
Chang, L.C.3
Tsai-Morris, C.H.4
Stamenkovich, D.5
Ferreira, P.C.6
Cohen, D.R.7
Edwards, S.A.8
Shows, T.B.9
Curran, T.10
Le Beau, M.M.11
Adamson, E.D.12
-
39
-
-
0030783859
-
dic(5;17): A recurring abnormality in malignant myeloid disorders associated with mutations of TP53
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 282-291
-
-
Wang, P.W.1
Spielberger, R.T.2
Thangavelu, M.3
Zhao, N.4
Davis, E.M.5
Iannantuoni, K.6
Larson, R.A.7
Le Beau, M.M.8
-
41
-
-
0027403024
-
Kelch encodes a component of intercellular bridges in Drosophila egg chambers
-
(1993)
Cell
, vol.72
, pp. 681-693
-
-
Xue, F.1
Cooley, L.2
-
44
-
-
0032532741
-
Human CDC23: cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias
-
(1998)
Genomics
, vol.53
, pp. 184-190
-
-
Zhao, N.1
Lai, F.2
Fernald, A.A.3
Eisenbart, J.D.4
Espinosa, R.5
Wang, P.W.6
Le Beau, M.M.7
|