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Items: 1 to 20 of 99

1.

Defining the heterochromatin localization and repression domains of SALL1.

Netzer C, Bohlander SK, Hinzke M, Chen Y, Kohlhase J.

Biochim Biophys Acta. 2006 Mar;1762(3):386-91. Epub 2006 Jan 6.

2.

SALL1, the gene mutated in Townes-Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin.

Netzer C, Rieger L, Brero A, Zhang CD, Hinzke M, Kohlhase J, Bohlander SK.

Hum Mol Genet. 2001 Dec 15;10(26):3017-24.

PMID:
11751684
3.

Sall1, a causative gene for Townes-Brocks syndrome, enhances the canonical Wnt signaling by localizing to heterochromatin.

Sato A, Kishida S, Tanaka T, Kikuchi A, Kodama T, Asashima M, Nishinakamura R.

Biochem Biophys Res Commun. 2004 Jun 18;319(1):103-13.

PMID:
15158448
4.
5.

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.

Kohlhase J, Wischermann A, Reichenbach H, Froster U, Engel W.

Nat Genet. 1998 Jan;18(1):81-3.

PMID:
9425907
6.

Molecular cloning, chromosomal localization, and expression of the murine SALL1 ortholog Sall1.

Buck A, Archangelo L, Dixkens C, Kohlhase J.

Cytogenet Cell Genet. 2000;89(3-4):150-3.

PMID:
10965108
7.

Molecular cloning of a SALL1-related pseudogene and mapping to chromosome Xp11.2.

Kohlhase J, Köhler A, Jäckle H, Engel W, Stick R.

Cytogenet Cell Genet. 1999;84(1-2):31-4.

PMID:
10343095
8.

SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype.

Botzenhart EM, Green A, Ilyina H, König R, Lowry RB, Lo IF, Shohat M, Burke L, McGaughran J, Chafai R, Pierquin G, Michaelis RC, Whiteford ML, Simola KO, Rösler B, Kohlhase J.

Hum Mutat. 2005 Sep;26(3):282.

PMID:
16088922
9.

Murine Sall1 represses transcription by recruiting a histone deacetylase complex.

Kiefer SM, McDill BW, Yang J, Rauchman M.

J Biol Chem. 2002 Apr 26;277(17):14869-76. Epub 2002 Feb 8.

10.
11.

SALL1 mutations in Townes-Brocks syndrome and related disorders.

Kohlhase J.

Hum Mutat. 2000 Dec;16(6):460-6. Review.

PMID:
11102974
12.

Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.

Kohlhase J, Taschner PE, Burfeind P, Pasche B, Newman B, Blanck C, Breuning MH, ten Kate LP, Maaswinkel-Mooy P, Mitulla B, Seidel J, Kirkpatrick SJ, Pauli RM, Wargowski DS, Devriendt K, Proesmans W, Gabrielli O, Coppa GV, Wesby-van Swaay E, Trembath RC, Schinzel AA, Reardon W, Seemanova E, Engel W.

Am J Hum Genet. 1999 Feb;64(2):435-45.

13.
14.

Identification of a novel BTB-zinc finger transcriptional repressor, CIBZ, that interacts with CtBP corepressor.

Sasai N, Matsuda E, Sarashina E, Ishida Y, Kawaichi M.

Genes Cells. 2005 Sep;10(9):871-85.

15.

A conserved 12-amino acid motif in Sall1 recruits the nucleosome remodeling and deacetylase corepressor complex.

Lauberth SM, Rauchman M.

J Biol Chem. 2006 Aug 18;281(33):23922-31. Epub 2006 May 17.

16.

SALL1 mutations in sporadic Townes-Brocks syndrome are of predominantly paternal origin without obvious paternal age effect.

Böhm J, Munk-Schulenburg S, Felscher S, Kohlhase J.

Am J Med Genet A. 2006 Sep 15;140(18):1904-8.

PMID:
16892410
17.

SALL3, a new member of the human spalt-like gene family, maps to 18q23.

Kohlhase J, Hausmann S, Stojmenovic G, Dixkens C, Bink K, Schulz-Schaeffer W, Altmann M, Engel W.

Genomics. 1999 Dec 1;62(2):216-22.

PMID:
10610715
18.

Zinc finger protein sall2 is not essential for embryonic and kidney development.

Sato A, Matsumoto Y, Koide U, Kataoka Y, Yoshida N, Yokota T, Asashima M, Nishinakamura R.

Mol Cell Biol. 2003 Jan;23(1):62-9.

19.

The nuclear receptor co-repressor (N-CoR) utilizes repression domains I and III for interaction and co-repression with ETO.

Lausen J, Cho S, Liu S, Werner MH.

J Biol Chem. 2004 Nov 19;279(47):49281-8. Epub 2004 Sep 17.

20.

Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient.

Marlin S, Blanchard S, Slim R, Lacombe D, Denoyelle F, Alessandri JL, Calzolari E, Drouin-Garraud V, Ferraz FG, Fourmaintraux A, Philip N, Toublanc JE, Petit C.

Hum Mutat. 1999;14(5):377-86.

PMID:
10533063

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