-
1
-
-
33745842538
-
Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor
-
COI: 1:CAS:528:DC%2BD28XmtFyks7Y%3D
-
Cho YS, Kim EJ, Park UH, Sin HS, Um SJ. Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor. JBC. 2006;281:17588–98.
-
(2006)
JBC
, vol.281
, pp. 17588-17598
-
-
Cho, Y.S.1
Kim, E.J.2
Park, U.H.3
Sin, H.S.4
Um, S.J.5
-
2
-
-
84855695098
-
The HARE-HTH and associated domains: novel modules in the coordination of epigenetic DNA and protein modifications
-
COI: 1:CAS:528:DC%2BC38XitVKlsrk%3D, PID: 22186017
-
Aravind L, Iyer LM. The HARE-HTH and associated domains: novel modules in the coordination of epigenetic DNA and protein modifications. Cell Cycle. 2012;11:119–31.
-
(2012)
Cell Cycle
, vol.11
, pp. 119-131
-
-
Aravind, L.1
Iyer, L.M.2
-
3
-
-
73649142039
-
ASXL1 represses retinoic acid receptor mediated transcription through associating with HP1 and LSD1
-
COI: 1:CAS:528:DC%2BD1MXhs1SqsbnF
-
Lee SW, Cho YS, Na JM, Park UH, Kang M, Kim EJ, et al. ASXL1 represses retinoic acid receptor mediated transcription through associating with HP1 and LSD1. JBC. 2010;285:18–29.
-
(2010)
JBC
, vol.285
, pp. 18-29
-
-
Lee, S.W.1
Cho, Y.S.2
Na, J.M.3
Park, U.H.4
Kang, M.5
Kim, E.J.6
-
4
-
-
35448944724
-
Prefrontal dysfunction in schizophrenia involves mixed-lineage leukemia 1-regulated histone methylation at GABAergic gene promoters
-
COI: 1:CAS:528:DC%2BD2sXht1ekur3J, PID: 17942719
-
Huang HS, Matevossian A, Whittle C, Kim SY, Schumacher A, Baker SP, et al. Prefrontal dysfunction in schizophrenia involves mixed-lineage leukemia 1-regulated histone methylation at GABAergic gene promoters. J Neurosci. 2007;27:11254–62.
-
(2007)
J Neurosci
, vol.27
, pp. 11254-11262
-
-
Huang, H.S.1
Matevossian, A.2
Whittle, C.3
Kim, S.Y.4
Schumacher, A.5
Baker, S.P.6
-
5
-
-
33846983276
-
Polycomb/Trithorax response elements and epigenetic memory of cell identity
-
COI: 1:CAS:528:DC%2BD2sXhvFGms7c%3D, PID: 17185323
-
Ringrose L, Paro R. Polycomb/Trithorax response elements and epigenetic memory of cell identity. Development. 2007;134:223–32.
-
(2007)
Development.
, vol.134
, pp. 223-232
-
-
Ringrose, L.1
Paro, R.2
-
6
-
-
33845799903
-
Polycomb silencing mechanisms and the management of genomic programmes
-
COI: 1:CAS:528:DC%2BD28Xhtlakt7fM, PID: 17173055
-
Schwartz YB, Pirrotta V. Polycomb silencing mechanisms and the management of genomic programmes. Nature Rev Genet. 2007;8:9–22.
-
(2007)
Nature Rev Genet.
, vol.8
, pp. 9-22
-
-
Schwartz, Y.B.1
Pirrotta, V.2
-
7
-
-
70450239681
-
Mutations of ASXL1 gene in myeloproliferative neoplasms
-
COI: 1:CAS:528:DC%2BD1MXhtl2hsrjJ, PID: 19609284
-
Carbuccia N, Murati A, Trouplin V, Brecqueville M, Adélaïde J, Rey J, et al. Mutations of ASXL1 gene in myeloproliferative neoplasms. Leukemia. 2009;23:2183–6.
-
(2009)
Leukemia
, vol.23
, pp. 2183-2186
-
-
Carbuccia, N.1
Murati, A.2
Trouplin, V.3
Brecqueville, M.4
Adélaïde, J.5
Rey, J.6
-
8
-
-
66849124925
-
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
-
COI: 1:CAS:528:DC%2BD1MXosVartbw%3D, PID: 19388938
-
Gelsi-Boyer V, Trouplin V, Adelaide J, Bonansea J, Cervera N, Carbuccia N, et al. Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia. Br J Haematol. 2009;145:788–800.
-
(2009)
Br J Haematol
, vol.145
, pp. 788-800
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Adelaide, J.3
Bonansea, J.4
Cervera, N.5
Carbuccia, N.6
-
9
-
-
84904392234
-
Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome
-
Chen TC, Hou HA, Chou WC, Tang JL, Kuo YY, Chen CY, et al. Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome. Blood Cancer J. 2014;4:177–85.
-
(2014)
Blood Cancer J
, vol.4
, pp. 177-185
-
-
Chen, T.C.1
Hou, H.A.2
Chou, W.C.3
Tang, J.L.4
Kuo, Y.Y.5
Chen, C.Y.6
-
10
-
-
79960909421
-
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome
-
COI: 1:CAS:528:DC%2BC3MXotV2jurw%3D, PID: 21706002
-
Hoischen A, van Bon BW, Rodriguez-Santiago B, Gilissen C, Vissers LE, de Vries P, et al. De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome. Nature Genet. 2011;43:729–31.
-
(2011)
Nature Genet.
, vol.43
, pp. 729-731
-
-
Hoischen, A.1
van Bon, B.W.2
Rodriguez-Santiago, B.3
Gilissen, C.4
Vissers, L.E.5
de Vries, P.6
-
11
-
-
84859005398
-
Two novel patients with Bohring-Opitz syndrome caused by de novo ASXL1 mutations
-
COI: 1:CAS:528:DC%2BC38XksFWrsL8%3D
-
Magini P, Della Monica M, Uzielli ML, Mongelli P, Scarselli G, Gambineri E, et al. Two novel patients with Bohring-Opitz syndrome caused by de novo ASXL1 mutations. Am J Med Genet. 2012;158:917–21.
-
(2012)
Am J Med Genet
, vol.158
, pp. 917-921
-
-
Magini, P.1
Della Monica, M.2
Uzielli, M.L.3
Mongelli, P.4
Scarselli, G.5
Gambineri, E.6
-
12
-
-
79959317767
-
Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes
-
COI: 1:CAS:528:DC%2BC3MXpsVyqtrw%3D, PID: 21576631
-
Thol F, Friesen I, Damm F, Yun H, Weissinger EM, Krauter J, et al. Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes. J Clin Oncol. 2011;29:2499–506.
-
(2011)
J Clin Oncol
, vol.29
, pp. 2499-2506
-
-
Thol, F.1
Friesen, I.2
Damm, F.3
Yun, H.4
Weissinger, E.M.5
Krauter, J.6
-
13
-
-
84857699307
-
Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value
-
COI: 1:CAS:528:DC%2BC3sXktFCksA%3D%3D
-
Pratcorona M, Abbas S, Sanders M, Koenders JE, Kavelaars FG, Erpelinck-Verschueren CA, et al. Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value. Hematologica. 2012;97:388–92.
-
(2012)
Hematologica.
, vol.97
, pp. 388-392
-
-
Pratcorona, M.1
Abbas, S.2
Sanders, M.3
Koenders, J.E.4
Kavelaars, F.G.5
Erpelinck-Verschueren, C.A.6
-
14
-
-
84858600403
-
Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases
-
COI: 1:CAS:528:DC%2BC38Xpt1ajtL0%3D, PID: 22436456
-
Gelsi-Boyer V, Brecqueville M, Devillier R, Murati A, Mozziconacci MJ, Birnbaum D. Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases. J Hematol Oncol. 2012;5:12–7.
-
(2012)
J Hematol Oncol.
, vol.5
, pp. 12-17
-
-
Gelsi-Boyer, V.1
Brecqueville, M.2
Devillier, R.3
Murati, A.4
Mozziconacci, M.J.5
Birnbaum, D.6
-
15
-
-
84922332658
-
ASXL1 and SETBP1 mutations and their prognostic contribution in chronic myelomonocytic leukemia: a two-center study of 466 patients
-
COI: 1:CAS:528:DC%2BC2cXmvV2gsLo%3D, PID: 24695057
-
Patnaik MM, Itzykson R, Lasho TL, Kosmider O, Finke CM, Hanson CA, et al. ASXL1 and SETBP1 mutations and their prognostic contribution in chronic myelomonocytic leukemia: a two-center study of 466 patients. Leukemia. 2014;28:2206–12.
-
(2014)
Leukemia
, vol.28
, pp. 2206-2212
-
-
Patnaik, M.M.1
Itzykson, R.2
Lasho, T.L.3
Kosmider, O.4
Finke, C.M.5
Hanson, C.A.6
-
16
-
-
79960227474
-
Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms
-
COI: 1:CAS:528:DC%2BC3MXoslOiurw%3D, PID: 21455215
-
Abdel-Wahab O, Pardanani A, Patel J, Wadleigh M, Lasho T, Heguy A, et al. Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms. Leukemia. 2011;25:1200–2.
-
(2011)
Leukemia
, vol.25
, pp. 1200-1202
-
-
Abdel-Wahab, O.1
Pardanani, A.2
Patel, J.3
Wadleigh, M.4
Lasho, T.5
Heguy, A.6
-
17
-
-
84555171449
-
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
-
PID: 22158541
-
Quesada V, Conde L, Villamor N, Ordóñez GR, Jares P, Bassaganyas L, et al. Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia. Nature Genet. 2011;44:47–52.
-
(2011)
Nature Genet.
, vol.44
, pp. 47-52
-
-
Quesada, V.1
Conde, L.2
Villamor, N.3
Ordóñez, G.R.4
Jares, P.5
Bassaganyas, L.6
-
18
-
-
33644537810
-
Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral
-
COI: 1:CAS:528:DC%2BD28XktlymtL4%3D, PID: 16014699
-
Tavtigian SV, Deffenbaugh AM, Yin L, Judkins T, Scholl T, Samollow PB, de Silva D, Thomas A, et al. Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral. J Med Genet. 2006;43:295–305.
-
(2006)
J Med Genet
, vol.43
, pp. 295-305
-
-
Tavtigian, S.V.1
Deffenbaugh, A.M.2
Yin, L.3
Judkins, T.4
Scholl, T.5
Samollow, P.B.6
de Silva, D.7
Thomas, A.8
-
19
-
-
11144331052
-
Computational prediction of binding hotspots Conf Proc IEEE
-
COI: 1:STN:280:DC%2BD2s%2FmslGjuw%3D%3D
-
Tong W, Li L, Weng Z. Computational prediction of binding hotspots Conf Proc IEEE. Eng Med Biol Soc. 2004;4:2980–3.
-
(2004)
Eng Med Biol Soc
, vol.4
, pp. 2980-2983
-
-
Tong, W.1
Li, L.2
Weng, Z.3
-
20
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
COI: 1:CAS:528:DC%2BC3cXjvFKqu78%3D, PID: 20354512
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, et al. A method and server for predicting damaging missense mutations. Nat Methods. 2010;7:248–9.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
-
21
-
-
84899508658
-
MEGA-MD: Molecular Evolutionary Genetics Analysis software with mutational diagnosis of amino acid variation
-
COI: 1:CAS:528:DC%2BC2cXmvFequrY%3D, PID: 24413669
-
Stecher G, Liu L, Sanderford M, Peterson D, Tamura K, Kumar S. MEGA-MD: Molecular Evolutionary Genetics Analysis software with mutational diagnosis of amino acid variation. Bioinformatics. 2014;30:1305–7.
-
(2014)
Bioinformatics
, vol.30
, pp. 1305-1307
-
-
Stecher, G.1
Liu, L.2
Sanderford, M.3
Peterson, D.4
Tamura, K.5
Kumar, S.6
-
22
-
-
0036269721
-
Genetic susceptibility to chronic lymphocytic leukemia
-
COI: 1:CAS:528:DC%2BD38XksFOnu7c%3D, PID: 12040432
-
Houlston RS, Catovsky D, Yuille MR. Genetic susceptibility to chronic lymphocytic leukemia. Leukemia. 2002;16:1008–14.
-
(2002)
Leukemia
, vol.16
, pp. 1008-1014
-
-
Houlston, R.S.1
Catovsky, D.2
Yuille, M.R.3
-
23
-
-
84862142857
-
Molecular study of the perforin gene in familial hematological malignancies
-
El Abed R, Bourdon V, Voskoboinik I, Omri H, Youssef YB, Laatiri MA, et al. Molecular study of the perforin gene in familial hematological malignancies. HCCP J. 2011;9:9–16.
-
(2011)
HCCP J
, vol.9
, pp. 9-16
-
-
El Abed, R.1
Bourdon, V.2
Voskoboinik, I.3
Omri, H.4
Youssef, Y.B.5
Laatiri, M.A.6
-
24
-
-
70449427713
-
Molecular study of CEPBA in familial hematological malignancies
-
PID: 19731081
-
El Abed R, Bourdon V, Huiart L, Eisinger F, Khelif A, Frenay M, et al. Molecular study of CEPBA in familial hematological malignancies. Fam Cancer. 2009;8:581–4.
-
(2009)
Fam Cancer
, vol.8
, pp. 581-584
-
-
El Abed, R.1
Bourdon, V.2
Huiart, L.3
Eisinger, F.4
Khelif, A.5
Frenay, M.6
-
25
-
-
84894666504
-
Cytogenetic and genetic mutation features of de novo acute myeloid leukemia in elderly chinese patients
-
PID: 24568515
-
Su L, Li X, Gao SJ, Yu P, Liu XL, Tan YH, et al. Cytogenetic and genetic mutation features of de novo acute myeloid leukemia in elderly chinese patients. Asian Pac J Cancer Prev. 2014;15:895–8.
-
(2014)
Asian Pac J Cancer Prev
, vol.15
, pp. 895-898
-
-
Su, L.1
Li, X.2
Gao, S.J.3
Yu, P.4
Liu, X.L.5
Tan, Y.H.6
-
26
-
-
84881108886
-
Functional and cancer genomics of ASXL family members
-
COI: 1:CAS:528:DC%2BC3sXhtFOit7jL, PID: 23736028
-
Katoh M. Functional and cancer genomics of ASXL family members. Br J Cancer. 2013;109:299–306.
-
(2013)
Br J Cancer
, vol.109
, pp. 299-306
-
-
Katoh, M.1
-
27
-
-
68049087052
-
Heterogeneous breakpoints in patients with acute lymphoblastic leukemia and the dic(9;20)(p11-13;q11) show recurrent involvement of genes at 20q11.21
-
COI: 1:CAS:528:DC%2BD1MXhtVymsbbN
-
An Q, Wright SL, Moorman AV, Parker H, Griffiths M, Ross FM, et al. Heterogeneous breakpoints in patients with acute lymphoblastic leukemia and the dic(9;20)(p11-13;q11) show recurrent involvement of genes at 20q11.21. Hematologica. 2009;94:1164–9.
-
(2009)
Hematologica
, vol.94
, pp. 1164-1169
-
-
An, Q.1
Wright, S.L.2
Moorman, A.V.3
Parker, H.4
Griffiths, M.5
Ross, F.M.6
-
28
-
-
84896930589
-
Oral extranodal non Hodgkin’s lymphoma: series of forty two cases in Malaysia
-
PID: 24641380
-
Ramanathan A, Mahmoud HAR, Hui LP, Mei NY, Valliappan V, Zain RB. Oral extranodal non Hodgkin’s lymphoma: series of forty two cases in Malaysia. Asian Pac J Cancer Prev. 2014;15:1633–7.
-
(2014)
Asian Pac J Cancer Prev
, vol.15
, pp. 1633-1637
-
-
Ramanathan, A.1
Mahmoud, H.A.R.2
Hui, L.P.3
Mei, N.Y.4
Valliappan, V.5
Zain, R.B.6
-
29
-
-
33745842538
-
Additional sex comb-like1(ASXL1) in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor
-
COI: 1:CAS:528:DC%2BD28XmtFyks7Y%3D, PID: 16606617
-
Cho YS, Kim EJ, Park UH, Sin HS, Um SJ. Additional sex comb-like1(ASXL1) in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor. J Biol Chem. 2006;281:17588–98.
-
(2006)
J Biol Chem
, vol.281
, pp. 17588-17598
-
-
Cho, Y.S.1
Kim, E.J.2
Park, U.H.3
Sin, H.S.4
Um, S.J.5
-
30
-
-
84896966469
-
All-trans-retinoic acid promotes iodine uptake via upregulating the sodium iodide symporter in medullary thyroid cancer stem cells
-
PID: 24641421
-
Tang M, Hou YL, Kang QQ, Chen XY, Duan LQ, Shu J, et al. All-trans-retinoic acid promotes iodine uptake via upregulating the sodium iodide symporter in medullary thyroid cancer stem cells. Asian Pac J Cancer Prev. 2014;15:1859–62.
-
(2014)
Asian Pac J Cancer Prev
, vol.15
, pp. 1859-1862
-
-
Tang, M.1
Hou, Y.L.2
Kang, Q.Q.3
Chen, X.Y.4
Duan, L.Q.5
Shu, J.6
|