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Results: 1 to 20 of 33

References for PMC Articles for PubMed (Select 10364509)

1.

Effects of altered gene order or orientation of the locus control region on human beta-globin gene expression in mice.

Tanimoto K, Liu Q, Bungert J, Engel JD.

Nature. 1999 Mar 25;398(6725):344-8.

PMID:
10192336
2.

A novel ubiquitination factor, E4, is involved in multiubiquitin chain assembly.

Koegl M, Hoppe T, Schlenker S, Ulrich HD, Mayer TU, Jentsch S.

Cell. 1999 Mar 5;96(5):635-44.

3.
4.

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects.

Yamagishi H, Garg V, Matsuoka R, Thomas T, Srivastava D.

Science. 1999 Feb 19;283(5405):1158-61.

5.

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.

Ohta T, Buiting K, Kokkonen H, McCandless S, Heeger S, Leisti H, Driscoll DJ, Cassidy SB, Horsthemke B, Nicholls RD.

Am J Hum Genet. 1999 Feb;64(2):385-96.

6.
7.

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.

8.

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.

9.

Ubiquitin, cellular inclusions and their role in neurodegeneration.

Alves-Rodrigues A, Gregori L, Figueiredo-Pereira ME.

Trends Neurosci. 1998 Dec;21(12):516-20. Review.

PMID:
9881849
10.
11.

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

Jiang YH, Armstrong D, Albrecht U, Atkins CM, Noebels JL, Eichele G, Sweatt JD, Beaudet AL.

Neuron. 1998 Oct;21(4):799-811.

12.

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

DeLorey TM, Handforth A, Anagnostaras SG, Homanics GE, Minassian BA, Asatourian A, Fanselow MS, Delgado-Escueta A, Ellison GD, Olsen RW.

J Neurosci. 1998 Oct 15;18(20):8505-14.

13.

The ubiquitin system.

Hershko A, Ciechanover A.

Annu Rev Biochem. 1998;67:425-79. Review.

PMID:
9759494
14.

Imprinting in Angelman and Prader-Willi syndromes.

Jiang Y, Tsai TF, Bressler J, Beaudet AL.

Curr Opin Genet Dev. 1998 Jun;8(3):334-42. Review.

PMID:
9691003
15.

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.

Buiting K, Dittrich B, Gross S, Lich C, Färber C, Buchholz T, Smith E, Reis A, Bürger J, Nöthen MM, Barth-Witte U, Janssen B, Abeliovich D, Lerer I, van den Ouweland AM, Halley DJ, Schrander-Stumpel C, Smeets H, Meinecke P, Malcolm S, Gardner A, Lalande M, Nicholls RD, Friend K, Schulze A, Matthijs G, Kokkonen H, Hilbert P, Van Maldergem L, Glover G, Carbonell P, Willems P, Gillessen-Kaesbach G, Horsthemke B.

Am J Hum Genet. 1998 Jul;63(1):170-80.

16.

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

Cummings CJ, Mancini MA, Antalffy B, DeFranco DB, Orr HT, Zoghbi HY.

Nat Genet. 1998 Jun;19(2):148-54.

PMID:
9620770
17.

Imprinting in Prader-Willi and Angelman syndromes.

Nicholls RD, Saitoh S, Horsthemke B.

Trends Genet. 1998 May;14(5):194-200. Review.

PMID:
9613204
18.

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript.

Rougeulle C, Cardoso C, Fontés M, Colleaux L, Lalande M.

Nat Genet. 1998 May;19(1):15-6. No abstract available.

PMID:
9590281
19.

Mutation analysis of UBE3A in Angelman syndrome patients.

Malzac P, Webber H, Moncla A, Graham JM, Kukolich M, Williams C, Pagon RA, Ramsdell LA, Kishino T, Wagstaff J.

Am J Hum Genet. 1998 Jun;62(6):1353-60.

20.

The itchy locus encodes a novel ubiquitin protein ligase that is disrupted in a18H mice.

Perry WL, Hustad CM, Swing DA, O'Sullivan TN, Jenkins NA, Copeland NG.

Nat Genet. 1998 Feb;18(2):143-6.

PMID:
9462742
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