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Items: 17

1.

14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome.

Toyo-oka K, Shionoya A, Gambello MJ, Cardoso C, Leventer R, Ward HL, Ayala R, Tsai LH, Dobyns W, Ledbetter D, Hirotsune S, Wynshaw-Boris A.

Nat Genet. 2003 Jul;34(3):274-85.

PMID:
12796778
2.
3.

Murine modelling of classical lissencephaly.

Gambello MJ, Hirotsune S, Wynshaw-Boris A.

Neurogenetics. 1999 Apr;2(2):77-86. Review.

PMID:
10369882
4.

Lissencephaly and the molecular basis of neuronal migration.

Kato M, Dobyns WB.

Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R89-96. Review.

PMID:
12668601
5.

LIS1 and dynein motor function in neuronal migration and development.

Wynshaw-Boris A, Gambello MJ.

Genes Dev. 2001 Mar 15;15(6):639-51. Review. No abstract available.

6.

[Molecular mechanism of lissencephaly--how LIS1 and NDEL1 regulate cytoplasmic dynein?].

Hirotsune S.

Brain Nerve. 2008 Apr;60(4):375-81. Review. Japanese.

PMID:
18421979
7.

LIS1 functions in normal development and disease.

Reiner O, Sapir T.

Curr Opin Neurobiol. 2013 Dec;23(6):951-6. doi: 10.1016/j.conb.2013.08.001. Epub 2013 Aug 23. Review.

PMID:
23973156
8.

Neuronal migration.

Lambert de Rouvroit C, Goffinet AM.

Mech Dev. 2001 Jul;105(1-2):47-56. Review.

9.

The role of cytoplasmic dynein in the human brain developmental disease lissencephaly.

Vallee RB, Faulkner NE, Tai CY.

Biochim Biophys Acta. 2000 Mar 17;1496(1):89-98. Review.

10.

LIS1-Associated Lissencephaly/Subcortical Band Heterotopia.

Dobyns WB, Das S.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2009 Mar 3 [updated 2014 Aug 14].

11.

Cytoskeleton in action: lissencephaly, a neuronal migration disorder.

Moon HM, Wynshaw-Boris A.

Wiley Interdiscip Rev Dev Biol. 2013 Mar-Apr;2(2):229-45. Review.

12.

Potential mechanisms of mutations that affect neuronal migration in man and mouse.

Walsh CA, Goffinet AM.

Curr Opin Genet Dev. 2000 Jun;10(3):270-4. Review.

PMID:
10826984
13.

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.

Dobyns WB, Reiner O, Carrozzo R, Ledbetter DH.

JAMA. 1993 Dec 15;270(23):2838-42. Review.

PMID:
7907669
14.

Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).

Cardoso C, Leventer RJ, Dowling JJ, Ward HL, Chung J, Petras KS, Roseberry JA, Weiss AM, Das S, Martin CL, Pilz DT, Dobyns WB, Ledbetter DH.

Hum Mutat. 2002 Jan;19(1):4-15. Review.

PMID:
11754098
15.

[Genetic and clinical aspects of lissencephaly].

Verloes A, Elmaleh M, Gonzales M, Laquerrière A, Gressens P.

Rev Neurol (Paris). 2007 May;163(5):533-47. Review. French.

PMID:
17571022
16.

Genetic factors in lissencephaly syndromes: a review.

Miny P, Holzgreve W, Horst J.

Childs Nerv Syst. 1993 Nov;9(7):413-7. Review.

PMID:
8306358
17.

[Neuronal migration and Cdk5].

Ohshima T.

Tanpakushitsu Kakusan Koso. 2009 Jun;54(7):796-801. Review. Japanese. No abstract available.

PMID:
19514264

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