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Items: 1 to 20 of 38

1.

Oncofetal gene SALL4 in aggressive hepatocellular carcinoma.

Yong KJ, Gao C, Lim JS, Yan B, Yang H, Dimitrov T, Kawasaki A, Ong CW, Wong KF, Lee S, Ravikumar S, Srivastava S, Tian X, Poon RT, Fan ST, Luk JM, Dan YY, Salto-Tellez M, Chai L, Tenen DG.

N Engl J Med. 2013 Jun 13;368(24):2266-76. doi: 10.1056/NEJMoa1300297.

2.

Targeting transcription factor SALL4 in acute myeloid leukemia by interrupting its interaction with an epigenetic complex.

Gao C, Dimitrov T, Yong KJ, Tatetsu H, Jeong HW, Luo HR, Bradner JE, Tenen DG, Chai L.

Blood. 2013 Feb 21;121(8):1413-21. doi: 10.1182/blood-2012-04-424275. Epub 2013 Jan 3.

3.

Exon-level array CGH in a large clinical cohort demonstrates increased sensitivity of diagnostic testing for Mendelian disorders.

Aradhya S, Lewis R, Bonaga T, Nwokekeh N, Stafford A, Boggs B, Hruska K, Smaoui N, Compton JG, Richard G, Suchy S.

Genet Med. 2012 Jun;14(6):594-603. doi: 10.1038/gim.2011.65. Epub 2012 Mar 1.

PMID:
22382802
4.

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.

Albers CA, Paul DS, Schulze H, Freson K, Stephens JC, Smethurst PA, Jolley JD, Cvejic A, Kostadima M, Bertone P, Breuning MH, Debili N, Deloukas P, Favier R, Fiedler J, Hobbs CM, Huang N, Hurles ME, Kiddle G, Krapels I, Nurden P, Ruivenkamp CA, Sambrook JG, Smith K, Stemple DL, Strauss G, Thys C, van Geet C, Newbury-Ecob R, Ouwehand WH, Ghevaert C.

Nat Genet. 2012 Feb 26;44(4):435-9, S1-2. doi: 10.1038/ng.1083.

5.

Human gene copy number spectra analysis in congenital heart malformations.

Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME.

Physiol Genomics. 2012 May 1;44(9):518-41. doi: 10.1152/physiolgenomics.00013.2012. Epub 2012 Feb 7.

6.

SALL4, a stem cell factor, affects the side population by regulation of the ATP-binding cassette drug transport genes.

Jeong HW, Cui W, Yang Y, Lu J, He J, Li A, Song D, Guo Y, Liu BH, Chai L.

PLoS One. 2011 Apr 19;6(4):e18372. doi: 10.1371/journal.pone.0018372.

7.

Stem cell factor SALL4 represses the transcriptions of PTEN and SALL1 through an epigenetic repressor complex.

Lu J, Jeong HW, Kong N, Yang Y, Carroll J, Luo HR, Silberstein LE, Yupoma, Chai L.

PLoS One. 2009;4(5):e5577. doi: 10.1371/journal.pone.0005577. Epub 2009 May 18. Erratum in: PLoS One. 2009;4(7). doi: 10.1371/annotation/e0bd3a57-1ce4-4eaf-83de-034d39cac787. Jeong, Hawon [corrected to Jeong, Ha-Won].

8.

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.

Mefford HC, Sharp AJ, Baker C, Itsara A, Jiang Z, Buysse K, Huang S, Maloney VK, Crolla JA, Baralle D, Collins A, Mercer C, Norga K, de Ravel T, Devriendt K, Bongers EM, de Leeuw N, Reardon W, Gimelli S, Bena F, Hennekam RC, Male A, Gaunt L, Clayton-Smith J, Simonic I, Park SM, Mehta SG, Nik-Zainal S, Woods CG, Firth HV, Parkin G, Fichera M, Reitano S, Lo Giudice M, Li KE, Casuga I, Broomer A, Conrad B, Schwerzmann M, Räber L, Gallati S, Striano P, Coppola A, Tolmie JL, Tobias ES, Lilley C, Armengol L, Spysschaert Y, Verloo P, De Coene A, Goossens L, Mortier G, Speleman F, van Binsbergen E, Nelen MR, Hochstenbach R, Poot M, Gallagher L, Gill M, McClellan J, King MC, Regan R, Skinner C, Stevenson RE, Antonarakis SE, Chen C, Estivill X, Menten B, Gimelli G, Gribble S, Schwartz S, Sutcliffe JS, Walsh T, Knight SJ, Sebat J, Romano C, Schwartz CE, Veltman JA, de Vries BB, Vermeesch JR, Barber JC, Willatt L, Tassabehji M, Eichler EE.

N Engl J Med. 2008 Oct 16;359(16):1685-99. doi: 10.1056/NEJMoa0805384. Epub 2008 Sep 10.

9.

Sall4 isoforms act during proximal-distal and anterior-posterior axis formation in the mouse embryo.

Uez N, Lickert H, Kohlhase J, de Angelis MH, Kühn R, Wurst W, Floss T.

Genesis. 2008 Sep;46(9):463-77. doi: 10.1002/dvg.20421.

PMID:
18781635
10.

SALL4 is a key regulator of survival and apoptosis in human leukemic cells.

Yang J, Chai L, Gao C, Fowles TC, Alipio Z, Dang H, Xu D, Fink LM, Ward DC, Ma Y.

Blood. 2008 Aug 1;112(3):805-13. doi: 10.1182/blood-2007-11-126326. Epub 2008 May 16. Erratum in: Blood. 2009 Oct 1; 114(14):3131.

11.

Multigene deletions on chromosome 20q13.13-q13.2 including SALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay.

Borozdin W, Graham JM Jr, Böhm D, Bamshad MJ, Spranger S, Burke L, Leipoldt M, Kohlhase J.

Hum Mutat. 2007 Aug;28(8):830.

PMID:
17623483
12.

Bmi-1 is a target gene for SALL4 in hematopoietic and leukemic cells.

Yang J, Chai L, Liu F, Fink LM, Lin P, Silberstein LE, Amin HM, Ward DC, Ma Y.

Proc Natl Acad Sci U S A. 2007 Jun 19;104(25):10494-9. Epub 2007 Jun 8.

13.

IVIC syndrome is caused by a c.2607delA mutation in the SALL4 locus.

Paradisi I, Arias S.

Am J Med Genet A. 2007 Feb 15;143(4):326-32.

PMID:
17256792
14.

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.

Klopocki E, Schulze H, Strauss G, Ott CE, Hall J, Trotier F, Fleischhauer S, Greenhalgh L, Newbury-Ecob RA, Neumann LM, Habenicht R, König R, Seemanova E, Megarbane A, Ropers HH, Ullmann R, Horn D, Mundlos S.

Am J Hum Genet. 2007 Feb;80(2):232-40. Epub 2006 Dec 21.

15.

Murine inner cell mass-derived lineages depend on Sall4 function.

Elling U, Klasen C, Eisenberger T, Anlag K, Treier M.

Proc Natl Acad Sci U S A. 2006 Oct 31;103(44):16319-24. Epub 2006 Oct 23.

16.

SALL4 is directly activated by TCF/LEF in the canonical Wnt signaling pathway.

Böhm J, Sustmann C, Wilhelm C, Kohlhase J.

Biochem Biophys Res Commun. 2006 Sep 29;348(3):898-907. Epub 2006 Jul 31.

PMID:
16899215
17.

Sall4 interacts with Nanog and co-occupies Nanog genomic sites in embryonic stem cells.

Wu Q, Chen X, Zhang J, Loh YH, Low TY, Zhang W, Zhang W, Sze SK, Lim B, Ng HH.

J Biol Chem. 2006 Aug 25;281(34):24090-4. Epub 2006 Jul 13.

18.

The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development.

Sakaki-Yumoto M, Kobayashi C, Sato A, Fujimura S, Matsumoto Y, Takasato M, Kodama T, Aburatani H, Asashima M, Yoshida N, Nishinakamura R.

Development. 2006 Aug;133(15):3005-13. Epub 2006 Jun 21.

19.

sall4 acts downstream of tbx5 and is required for pectoral fin outgrowth.

Harvey SA, Logan MP.

Development. 2006 Mar;133(6):1165-73.

20.

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