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Items: 1 to 20 of 183

1.

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
2.

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
3.

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
4.
5.

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.

6.

Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects.

Kiefer SM, Ohlemiller KK, Yang J, McDill BW, Kohlhase J, Rauchman M.

Hum Mol Genet. 2003 Sep 1;12(17):2221-7. Epub 2003 Jul 15.

PMID:
12915476
7.

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.

8.

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
9.

Interaction with members of the heterochromatin protein 1 (HP1) family and histone deacetylation are differentially involved in transcriptional silencing by members of the TIF1 family.

Nielsen AL, Ortiz JA, You J, Oulad-Abdelghani M, Khechumian R, Gansmuller A, Chambon P, Losson R.

EMBO J. 1999 Nov 15;18(22):6385-95.

10.

Targeting of Krüppel-associated box-containing zinc finger proteins to centromeric heterochromatin. Implication for the gene silencing mechanisms.

Matsuda E, Agata Y, Sugai M, Katakai T, Gonda H, Shimizu A.

J Biol Chem. 2001 Apr 27;276(17):14222-9. Epub 2001 Jan 19.

11.

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.

12.

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
13.

RLF2, a subunit of yeast chromatin assembly factor-I, is required for telomeric chromatin function in vivo.

Enomoto S, McCune-Zierath PD, Gerami-Nejad M, Sanders MA, Berman J.

Genes Dev. 1997 Feb 1;11(3):358-70.

14.
15.

Heterochromatin dynamics in mouse cells: interaction between chromatin assembly factor 1 and HP1 proteins.

Murzina N, Verreault A, Laue E, Stillman B.

Mol Cell. 1999 Oct;4(4):529-40.

16.

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
17.

SALL1 mutations in Townes-Brocks syndrome and related disorders.

Kohlhase J.

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

PMID:
11102974
18.

Interaction of the developmental regulator SALL1 with UBE2I and SUMO-1.

Netzer C, Bohlander SK, Rieger L, Müller S, Kohlhase J.

Biochem Biophys Res Commun. 2002 Aug 30;296(4):870-6.

PMID:
12200128
19.

Cell differentiation induces TIF1beta association with centromeric heterochromatin via an HP1 interaction.

Cammas F, Oulad-Abdelghani M, Vonesch JL, Huss-Garcia Y, Chambon P, Losson R.

J Cell Sci. 2002 Sep 1;115(Pt 17):3439-48.

20.

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