[cite web | title = Entrez Gene: SALL1 sal-like 1 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6299| accessdate = ] ] PBB_Summary
section_title =
summary_text =
References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Nishinakamura R, Takasato M |title=Essential roles of Sall1 in kidney development. |journal=Kidney Int. |volume=68 |issue= 5 |pages= 1948–50 |year= 2006 |pmid= 16221172 |doi= 10.1111/j.1523-1755.2005.00626.x
*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=Kohlhase J, Schuh R, Dowe G, "et al." |title=Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt. |journal=Genomics |volume=38 |issue= 3 |pages= 291–8 |year= 1997 |pmid= 8975705 |doi= 10.1006/geno.1996.0631
*cite journal | author=Kohlhase J, Wischermann A, Reichenbach H, "et al." |title=Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome. |journal=Nat. Genet. |volume=18 |issue= 1 |pages= 81–3 |year= 1998 |pmid= 9425907 |doi= 10.1038/ng0198-81
*cite journal | author=Kohlhase J, Taschner PE, Burfeind P, "et al." |title=Molecular analysis of SALL1 mutations in Townes-Brocks syndrome. |journal=Am. J. Hum. Genet. |volume=64 |issue= 2 |pages= 435–45 |year= 1999 |pmid= 9973281 |doi=
*cite journal | author=Marlin S, Blanchard S, Slim R, "et al." |title=Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient. |journal=Hum. Mutat. |volume=14 |issue= 5 |pages= 377–86 |year= 2000 |pmid= 10533063 |doi= 10.1002/(SICI)1098-1004(199911)14:5<377::AID-HUMU3>3.0.CO;2-A |doilabel=10.1002/(SICI)1098-1004(199911)14:5377::AID-HUMU33.0.CO;2-A
*cite journal | author=Engels S, Kohlhase J, McGaughran J |title=A SALL1 mutation causes a branchio-oto-renal syndrome-like phenotype. |journal=J. Med. Genet. |volume=37 |issue= 6 |pages= 458–60 |year= 2000 |pmid= 10928856 |doi=
*cite journal | author=Buck A, Archangelo L, Dixkens C, Kohlhase J |title=Molecular cloning, chromosomal localization, and expression of the murine SALL1 ortholog Sall1. |journal=Cytogenet. Cell Genet. |volume=89 |issue= 3-4 |pages= 150–3 |year= 2000 |pmid= 10965108 |doi=
*cite journal | author=Surka WS, Kohlhase J, Neunert CE, "et al." |title=Unique family with Townes-Brocks syndrome, SALL1 mutation, and cardiac defects. |journal=Am. J. Med. Genet. |volume=102 |issue= 3 |pages= 250–7 |year= 2001 |pmid= 11484202 |doi=
*cite journal | author=Netzer C, Rieger L, Brero A, "et al." |title=SALL1, the gene mutated in Townes-Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin. |journal=Hum. Mol. Genet. |volume=10 |issue= 26 |pages= 3017–24 |year= 2002 |pmid= 11751684 |doi=
*cite journal | author=Kiefer SM, McDill BW, Yang J, Rauchman M |title=Murine Sall1 represses transcription by recruiting a histone deacetylase complex. |journal=J. Biol. Chem. |volume=277 |issue= 17 |pages= 14869–76 |year= 2002 |pmid= 11836251 |doi= 10.1074/jbc.M200052200
*cite journal | author=Ma Y, Chai L, Cortez SC, "et al." |title=SALL1 expression in the human pituitary-adrenal/gonadal axis. |journal=J. Endocrinol. |volume=173 |issue= 3 |pages= 437–48 |year= 2002 |pmid= 12065233 |doi=
*cite journal | author=Netzer C, Bohlander SK, Rieger L, "et al." |title=Interaction of the developmental regulator SALL1 with UBE2I and SUMO-1. |journal=Biochem. Biophys. Res. Commun. |volume=296 |issue= 4 |pages= 870–6 |year= 2002 |pmid= 12200128 |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=Sato A, Kishida S, Tanaka T, "et al." |title=Sall1, a causative gene for Townes-Brocks syndrome, enhances the canonical Wnt signaling by localizing to heterochromatin. |journal=Biochem. Biophys. Res. Commun. |volume=319 |issue= 1 |pages= 103–13 |year= 2004 |pmid= 15158448 |doi= 10.1016/j.bbrc.2004.04.156
*cite journal | author=Suzuki Y, Yamashita R, Shirota M, "et al." |title=Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions. |journal=Genome Res. |volume=14 |issue= 9 |pages= 1711–8 |year= 2004 |pmid= 15342556 |doi= 10.1101/gr.2435604
*cite journal | author=Botzenhart EM, Green A, Ilyina H, "et al." |title=SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype. |journal=Hum. Mutat. |volume=26 |issue= 3 |pages= 282 |year= 2006 |pmid= 16088922 |doi= 10.1002/humu.9362
*cite journal | author=Kimura K, Wakamatsu A, Suzuki Y, "et al." |title=Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. |journal=Genome Res. |volume=16 |issue= 1 |pages= 55–65 |year= 2006 |pmid= 16344560 |doi= 10.1101/gr.4039406
*cite journal | author=Borozdin W, Steinmann K, Albrecht B, "et al." |title=Detection of heterozygous SALL1 deletions by quantitative real time PCR proves the contribution of a SALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome. |journal=Hum. Mutat. |volume=27 |issue= 2 |pages= 211–2 |year= 2006 |pmid= 16429401 |doi= 10.1002/humu.9396
PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes
