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Items: 1 to 20 of 62

1.

The human E6-AP gene (UBE3A) encodes three potential protein isoforms generated by differential splicing.

Yamamoto Y, Huibregtse JM, Howley PM.

Genomics. 1997 Apr 15;41(2):263-6.

PMID:
9143503
2.

The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region.

Sutcliffe JS, Jiang YH, Galijaard RJ, Matsuura T, Fang P, Kubota T, Christian SL, Bressler J, Cattanach B, Ledbetter DH, Beaudet AL.

Genome Res. 1997 Apr;7(4):368-77.

3.

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

Matsuura T, Sutcliffe JS, Fang P, Galjaard RJ, Jiang YH, Benton CS, Rommens JM, Beaudet AL.

Nat Genet. 1997 Jan;15(1):74-7.

PMID:
8988172
4.

The Angelman syndrome-associated protein, E6-AP, is a coactivator for the nuclear hormone receptor superfamily.

Nawaz Z, Lonard DM, Smith CL, Lev-Lehman E, Tsai SY, Tsai MJ, O'Malley BW.

Mol Cell Biol. 1999 Feb;19(2):1182-9.

5.

Genomic organization of the UBE3A/E6-AP gene and related pseudogenes.

Kishino T, Wagstaff J.

Genomics. 1998 Jan 1;47(1):101-7.

PMID:
9465301
6.

Cloning of human ubiquitin-conjugating enzymes UbcH6 and UbcH7 (E2-F1) and characterization of their interaction with E6-AP and RSP5.

Nuber U, Schwarz S, Kaiser P, Schneider R, Scheffner M.

J Biol Chem. 1996 Feb 2;271(5):2795-800.

7.

Identification of a human ubiquitin-conjugating enzyme that mediates the E6-AP-dependent ubiquitination of p53.

Scheffner M, Huibregtse JM, Howley PM.

Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):8797-801.

8.

UBE3A/E6-AP mutations cause Angelman syndrome.

Kishino T, Lalande M, Wagstaff J.

Nat Genet. 1997 Jan;15(1):70-3. Erratum in: Nat Genet 1997 Apr;15(4):411.

PMID:
8988171
9.

E6-AP/UBE3A protein acts as a ubiquitin ligase toward SOX9 protein.

Hattori T, Kishino T, Stephen S, Eberspaecher H, Maki S, Takigawa M, de Crombrugghe B, Yasuda H.

J Biol Chem. 2013 Dec 6;288(49):35138-48. doi: 10.1074/jbc.M113.486795. Epub 2013 Oct 23.

10.

A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase.

Huibregtse JM, Scheffner M, Beaudenon S, Howley PM.

Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2563-7. Erratum in: Proc Natl Acad Sci U S A. 1995 May 23;92(11):5249.

11.

The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53.

Scheffner M, Huibregtse JM, Vierstra RD, Howley PM.

Cell. 1993 Nov 5;75(3):495-505.

PMID:
8221889
12.
13.

The ubiquitin-protein ligase E6-associated protein (E6-AP) serves as its own substrate.

Nuber U, Schwarz SE, Scheffner M.

Eur J Biochem. 1998 Jun 15;254(3):643-9.

14.

Angelman syndrome: how many genes to remain silent?

Rougeulle C, Lalande M.

Neurogenetics. 1998 Aug;1(4):229-37. Review.

PMID:
10732796
16.
17.

Mutation screening of the UBE3A/E6-AP gene in autistic disorder.

Veenstra-VanderWeele J, Gonen D, Leventhal BL, Cook EH Jr.

Mol Psychiatry. 1999 Jan;4(1):64-7.

PMID:
10089011
18.

The spectrum of mutations in UBE3A causing Angelman syndrome.

Fang P, Lev-Lehman E, Tsai TF, Matsuura T, Benton CS, Sutcliffe JS, Christian SL, Kubota T, Halley DJ, Meijers-Heijboer H, Langlois S, Graham JM Jr, Beuten J, Willems PJ, Ledbetter DH, Beaudet AL.

Hum Mol Genet. 1999 Jan;8(1):129-35.

PMID:
9887341
19.

Protein ubiquitination involving an E1-E2-E3 enzyme ubiquitin thioester cascade.

Scheffner M, Nuber U, Huibregtse JM.

Nature. 1995 Jan 5;373(6509):81-3.

PMID:
7800044
20.

Role of ubiquitin and the HPV E6 oncoprotein in E6AP-mediated ubiquitination.

Mortensen F, Schneider D, Barbic T, Sladewska-Marquardt A, Kühnle S, Marx A, Scheffner M.

Proc Natl Acad Sci U S A. 2015 Aug 11;112(32):9872-7. doi: 10.1073/pnas.1505923112. Epub 2015 Jul 27.

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