SALL4


SALL4

Sal-like 4 (Drosophila), also known as SALL4, is a human gene.cite web | title = Entrez Gene: SALL4 sal-like 4 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57167| accessdate = ]

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section_title =
summary_text = Sal-like genes encode putative zinc finger transcription factors. For background information on SALL genes, see SALL1 (MIM 602218). [supplied by OMIM] cite web | title = Entrez Gene: SALL4 sal-like 4 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57167| accessdate = ]

References

Further reading

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citations =
*cite journal | author=Sweetman D, Münsterberg A |title=The vertebrate spalt genes in development and disease. |journal=Dev. Biol. |volume=293 |issue= 2 |pages= 285–93 |year= 2006 |pmid= 16545361 |doi= 10.1016/j.ydbio.2006.02.009
*cite journal | author=Deloukas P, Matthews LH, Ashurst J, "et al." |title=The DNA sequence and comparative analysis of human chromosome 20. |journal=Nature |volume=414 |issue= 6866 |pages= 865–71 |year= 2002 |pmid= 11780052 |doi= 10.1038/414865a
*cite journal | author=Kohlhase J, Heinrich M, Schubert L, "et al." |title=Okihiro syndrome is caused by SALL4 mutations. |journal=Hum. Mol. Genet. |volume=11 |issue= 23 |pages= 2979–87 |year= 2003 |pmid= 12393809 |doi=
*cite journal | author=Al-Baradie R, Yamada K, St Hilaire C, "et al." |title=Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family. |journal=Am. J. Hum. Genet. |volume=71 |issue= 5 |pages= 1195–9 |year= 2003 |pmid= 12395297 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Kohlhase J, Schubert L, Liebers M, "et al." |title=Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy. |journal=J. Med. Genet. |volume=40 |issue= 7 |pages= 473–8 |year= 2003 |pmid= 12843316 |doi=
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Borozdin W, Wright MJ, Hennekam RC, "et al." |title=Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum. |journal=J. Med. Genet. |volume=41 |issue= 8 |pages= e102 |year= 2004 |pmid= 15286162 |doi= 10.1136/jmg.2004.019505
*cite journal | author=Kohlhase J, Holmes LB |title=Mutations in SALL4 in malformed father and daughter postulated previously due to reflect mutagenesis by thalidomide. |journal=Birth Defects Res. Part A Clin. Mol. Teratol. |volume=70 |issue= 8 |pages= 550–1 |year= 2005 |pmid= 15329836 |doi= 10.1002/bdra.20050
*cite journal | author=Borozdin W, Boehm D, Leipoldt M, "et al." |title=SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism. |journal=J. Med. Genet. |volume=41 |issue= 9 |pages= e113 |year= 2005 |pmid= 15342710 |doi= 10.1136/jmg.2004.019901
*cite journal | author=Wabbels BK, Lorenz B, Kohlhase J |title=No evidence of SALL4-mutations in isolated sporadic duane retraction "syndrome" (DURS). |journal=Am. J. Med. Genet. A |volume=131 |issue= 2 |pages= 216–8 |year= 2005 |pmid= 15386473 |doi= 10.1002/ajmg.a.30321
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Kohlhase J, Chitayat D, Kotzot D, "et al." |title=SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders. |journal=Hum. Mutat. |volume=26 |issue= 3 |pages= 176–83 |year= 2006 |pmid= 16086360 |doi= 10.1002/humu.20215
*cite journal | author=Miertus J, Borozdin W, Frecer V, "et al." |title=A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndrome. |journal=Hum. Genet. |volume=119 |issue= 1-2 |pages= 154–61 |year= 2007 |pmid= 16402211 |doi= 10.1007/s00439-005-0124-7
*cite journal | author=Terhal P, Rösler B, Kohlhase J |title=A family with features overlapping Okihiro syndrome, hemifacial microsomia and isolated Duane anomaly caused by a novel SALL4 mutation. |journal=Am. J. Med. Genet. A |volume=140 |issue= 3 |pages= 222–6 |year= 2006 |pmid= 16411190 |doi= 10.1002/ajmg.a.31060
*cite journal | author=Ma Y, Cui W, Yang J, "et al." |title=SALL4, a novel oncogene, is constitutively expressed in human acute myeloid leukemia (AML) and induces AML in transgenic mice. |journal=Blood |volume=108 |issue= 8 |pages= 2726–35 |year= 2006 |pmid= 16763212 |doi= 10.1182/blood-2006-02-001594
*cite journal | author=Paradisi I, Arias S |title=IVIC syndrome is caused by a c.2607delA mutation in the SALL4 locus. |journal=Am. J. Med. Genet. A |volume=143 |issue= 4 |pages= 326–32 |year= 2007 |pmid= 17256792 |doi= 10.1002/ajmg.a.31603
*cite journal | author=Habano W, Sugai T, Jiao YF, Nakamura S |title=Novel approach for detecting global epigenetic alterations associated with tumor cell aneuploidy. |journal=Int. J. Cancer |volume=121 |issue= 7 |pages= 1487–93 |year= 2007 |pmid= 17546590 |doi= 10.1002/ijc.22847
*cite journal | author=Yang J, Chai L, Liu F, "et al." |title=Bmi-1 is a target gene for SALL4 in hematopoietic and leukemic cells. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=104 |issue= 25 |pages= 10494–9 |year= 2007 |pmid= 17557835 |doi= 10.1073/pnas.0704001104

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