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Similar articles for PubMed (Select 20806366)

1.

T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6.

Chao MM, Todd MA, Kontny U, Neas K, Sullivan MJ, Hunter AG, Picketts DJ, Kratz CP.

Pediatr Blood Cancer. 2010 Oct;55(4):722-4. doi: 10.1002/pbc.22574.

2.

Structural and functional insights into the human Börjeson-Forssman-Lehmann syndrome-associated protein PHF6.

Liu Z, Li F, Ruan K, Zhang J, Mei Y, Wu J, Shi Y.

J Biol Chem. 2014 Apr 4;289(14):10069-83. doi: 10.1074/jbc.M113.535351. Epub 2014 Feb 19.

3.

Börjeson-Forssman-Lehmann Syndrome due to a novel plant homeodomain zinc finger mutation in the PHF6 gene.

Mangelsdorf M, Chevrier E, Mustonen A, Picketts DJ.

J Child Neurol. 2009 May;24(5):610-4. doi: 10.1177/0883073808327830. Epub 2009 Mar 4.

PMID:
19264739
4.

Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity.

Voss AK, Gamble R, Collin C, Shoubridge C, Corbett M, Gécz J, Thomas T.

Gene Expr Patterns. 2007 Oct;7(8):858-71. Epub 2007 Jul 6.

PMID:
17698420
5.

A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype.

Zweier C, Kraus C, Brueton L, Cole T, Degenhardt F, Engels H, Gillessen-Kaesbach G, Graul-Neumann L, Horn D, Hoyer J, Just W, Rauch A, Reis A, Wollnik B, Zeschnigk M, Lüdecke HJ, Wieczorek D.

J Med Genet. 2013 Dec;50(12):838-47. doi: 10.1136/jmedgenet-2013-101918. Epub 2013 Oct 3.

PMID:
24092917
6.

Mutation screening in Borjeson-Forssman-Lehmann syndrome: identification of a novel de novo PHF6 mutation in a female patient.

Crawford J, Lower KM, Hennekam RC, Van Esch H, Mégarbané A, Lynch SA, Turner G, Gécz J.

J Med Genet. 2006 Mar;43(3):238-43. Epub 2005 Jul 1.

7.

Further clinical delineation of the Börjeson-Forssman-Lehmann syndrome in patients with PHF6 mutations.

Carter MT, Picketts DJ, Hunter AG, Graham GE.

Am J Med Genet A. 2009 Feb;149A(2):246-50. doi: 10.1002/ajmg.a.32624.

PMID:
19161141
8.

Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.

Zweier C, Rittinger O, Bader I, Berland S, Cole T, Degenhardt F, Di Donato N, Graul-Neumann L, Hoyer J, Lynch SA, Vlasak I, Wieczorek D.

Am J Med Genet C Semin Med Genet. 2014 Sep;166C(3):290-301. doi: 10.1002/ajmg.c.31408. Epub 2014 Aug 5. Review.

PMID:
25099957
9.

Structural basis of plant homeodomain finger 6 (PHF6) recognition by the retinoblastoma binding protein 4 (RBBP4) component of the nucleosome remodeling and deacetylase (NuRD) complex.

Liu Z, Li F, Zhang B, Li S, Wu J, Shi Y.

J Biol Chem. 2015 Mar 6;290(10):6630-8. doi: 10.1074/jbc.M114.610196. Epub 2015 Jan 19.

PMID:
25601084
10.

Mutations of PHF6 are associated with mutations of NOTCH1, JAK1 and rearrangement of SET-NUP214 in T-cell acute lymphoblastic leukemia.

Wang Q, Qiu H, Jiang H, Wu L, Dong S, Pan J, Wang W, Ping N, Xia J, Sun A, Wu D, Xue Y, Drexler HG, Macleod RA, Chen S.

Haematologica. 2011 Dec;96(12):1808-14. doi: 10.3324/haematol.2011.043083. Epub 2011 Aug 31.

11.

Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome.

Lower KM, Turner G, Kerr BA, Mathews KD, Shaw MA, Gedeon AK, Schelley S, Hoyme HE, White SM, Delatycki MB, Lampe AK, Clayton-Smith J, Stewart H, van Ravenswaay CM, de Vries BB, Cox B, Grompe M, Ross S, Thomas P, Mulley JC, Gécz J.

Nat Genet. 2002 Dec;32(4):661-5. Epub 2002 Nov 4.

PMID:
12415272
12.

1H, 13C and 15N resonance assignments and secondary structure of the human PHF6-ePHD1 domain.

Bao Y, Liu Z, Zhang J, Wu J, Shi Y.

Biomol NMR Assign. 2015 Aug 19. [Epub ahead of print]

PMID:
26286319
13.

PHF6 Deletions May Cause Borjeson-Forssman-Lehmann Syndrome in Females.

Berland S, Alme K, Brendehaug A, Houge G, Hovland R.

Mol Syndromol. 2011 Sep;1(6):294-300. Epub 2011 Jul 19.

14.

PHF6 Degrees of Separation: The Multifaceted Roles of a Chromatin Adaptor Protein.

Todd MA, Ivanochko D, Picketts DJ.

Genes (Basel). 2015 Jun 19;6(2):325-52. doi: 10.3390/genes6020325. Review.

15.

Somatic mutation of PHF6 gene in T-cell acute lymphoblatic leukemia, acute myelogenous leukemia and hepatocellular carcinoma.

Yoo NJ, Kim YR, Lee SH.

Acta Oncol. 2012 Jan;51(1):107-11. doi: 10.3109/0284186X.2011.592148. Epub 2011 Jul 8.

PMID:
21736506
16.

PHF6 interacts with the nucleosome remodeling and deacetylation (NuRD) complex.

Todd MA, Picketts DJ.

J Proteome Res. 2012 Aug 3;11(8):4326-37. doi: 10.1021/pr3004369. Epub 2012 Jul 3.

PMID:
22720776
17.

1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family.

Lower KM, Solders G, Bondeson ML, Nelson J, Brun A, Crawford J, Malm G, Börjeson M, Turner G, Partington M, Gécz J.

Eur J Hum Genet. 2004 Oct;12(10):787-9. No abstract available.

18.

Distinct phenotype of PHF6 deletions in females.

Di Donato N, Isidor B, Lopez Cazaux S, Le Caignec C, Klink B, Kraus C, Schrock E, Hackmann K.

Eur J Med Genet. 2014 Feb;57(2-3):85-9. doi: 10.1016/j.ejmg.2013.12.003. Epub 2013 Dec 28.

PMID:
24380767
19.

Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6.

Visootsak J, Rosner B, Dykens E, Schwartz C, Hahn K, White SM, Szeftel R, Graham JM.

J Pediatr. 2004 Dec;145(6):819-25.

PMID:
15580208
20.

PHF6 mutations in T-cell acute lymphoblastic leukemia.

Van Vlierberghe P, Palomero T, Khiabanian H, Van der Meulen J, Castillo M, Van Roy N, De Moerloose B, Philippé J, González-García S, Toribio ML, Taghon T, Zuurbier L, Cauwelier B, Harrison CJ, Schwab C, Pisecker M, Strehl S, Langerak AW, Gecz J, Sonneveld E, Pieters R, Paietta E, Rowe JM, Wiernik PH, Benoit Y, Soulier J, Poppe B, Yao X, Cordon-Cardo C, Meijerink J, Rabadan R, Speleman F, Ferrando A.

Nat Genet. 2010 Apr;42(4):338-42. doi: 10.1038/ng.542. Epub 2010 Mar 14.

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