Sal-like 4 (Drosophila), also known as SALL4, is a human gene.cite web | title = Entrez Gene: SALL4 sal-like 4 (Drosophila)| url =| accessdate = ]

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 =| accessdate = ]


Further reading

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

update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes

Wikimedia Foundation. 2010.

Look at other dictionaries:

  • Duane-radial ray syndrome — Classification and external resources OMIM 607323 DiseasesDB 33688 Duane radial ray syndrome is a rare disorder that affects the ey …   Wikipedia

  • Okihiro-Syndrom — Das Okihiro Syndrom auch als (engl.) Duane Radial Ray Syndrom (DRRS) bezeichnet ist eine autosomal dominant vererbte Kombination von Fehlbildungen. Inhaltsverzeichnis 1 Symptome 2 Ursache 3 Prognose 4 …   Deutsch Wikipedia

  • Homeobox protein NANOG — See NANOG (computing) for the network operators group. Nanog homeobox Identifiers Symbols NANOG; External IDs …   Wikipedia

  • Chromosome 20 (human) — Chromosome 20 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 20 spans around 63 million base pairs (the building material of DNA) and represents between 2 and 2.5 percent of the… …   Wikipedia

  • Atriodigitale Dysplasie — Klassifikation nach ICD 10 Q87.2 Angeborene Fehlbildungssyndrome mit vorwiegender Beteiligung der Extremitäten Holt Oram Syndrom …   Deutsch Wikipedia

  • Holt-Oram-Syndrom — Klassifikation nach ICD 10 Q87.2 Angeborene Fehlbildungssyndrome mit vorwiegender Beteiligung der Extremitäten Holt Oram Syndrom …   Deutsch Wikipedia

  • Townes-Brocks-Syndrom — Das Townes Brocks Syndrom ist eine autosomal dominant vererbte Kombination von Fehlbildungen der Ohren, des Afters und der Daumen. Etwa die Hälfte der Fälle geht auch mit Nierenfehlbildungen einher. Inhaltsverzeichnis 1 Verbreitung 2 Ursache 3… …   Deutsch Wikipedia

  • NANOG — NANOG  это транскрипционный фактор, участвующий в самообновлении недифференцированных эмбриональных стволовых клеток. Содержание 1 Эмбриональные стволовые клетки 2 История …   Википедия

  • 20-я хромосома человека — Идиограмма 20 й хромосомы человека 20 я хромосома человека является частью генома человека и насчитывает более 63 млн пар оснований, что составляет от 2 до 2,5 % всего ДНК материала клетки …   Википедия

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”

We are using cookies for the best presentation of our site. Continuing to use this site, you agree with this.