Analysis of lissencephaly-causingLIS1mutations (Q57274984)

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2 November 2019

title

Analysis of lissencephaly-causing LIS1 mutations (English)

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2 November 2019

3

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Junken Aoki

6

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2 November 2019

Mitsuharu Hattori

7

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2 November 2019

Orly Reiner

10

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2 November 2019

author name string

T Sapir

1

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2 November 2019

M Eisenstein

2

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D Horesh

4

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2 November 2019

A Cahana

5

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2 November 2019

H Arai

8

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2 November 2019

K Inoue

9

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language of work or name

English

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publication date

1 December 1999

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2 November 2019

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2 November 2019

volume

266

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issue

3

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page(s)

1011-1020

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2 November 2019

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https://api.crossref.org/works/10.1046/J.1432-1327.1999.00942.X

The reeler gene encodes a protein with an EGF–like motif expressed by pioneer neurons

21 January 2018

1 reference

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Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice

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Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse

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Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death

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Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality

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1 reference

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A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

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1 reference

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Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

21 January 2018

1 reference

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

21 January 2018

1 reference

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Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome

21 January 2018

1 reference

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Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 January 2018

1 reference

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The ancient regulatory-protein family of WD-repeat proteins

21 January 2018

1 reference

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Repetitive segmental structure of the transducin beta subunit: homology with the CDC4 gene and identification of related mRNAs

21 January 2018

1 reference

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Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein beta subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00942.X

The structure of the G protein heterotrimer Gi alpha 1 beta 1 gamma 2

21 January 2018

1 reference

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Crystal structure of a G-protein beta gamma dimer at 2.1A resolution

21 January 2018

1 reference

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G protein heterodimers: new structures propel new questions

21 January 2018

1 reference

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Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00942.X

Platelet activating factor: a biologically active phosphoglyceride

21 January 2018

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Platelet-activating factor: a paracrine factor in preimplantation stages of reproduction?

21 January 2018

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Platelet-activating factor: receptors and signal transduction

21 January 2018

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Platelet activating factor and conception

21 January 2018

1 reference

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Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00942.X

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00942.X

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

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The 2.0 A crystal structure of a heterotrimeric G protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00942.X

Doublecortin, a stabilizer of microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1046/J.1432-1327.1999.00942.X

Biospecific interaction analysis using biosensor technology

21 January 2018

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BIAcore: a microchip-based system for analyzing the formation of macromolecular complexes

21 January 2018

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Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

21 January 2018

1 reference

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NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration

21 January 2018

1 reference

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Association of a human G-protein beta3 subunit variant with hypertension

21 January 2018

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Platelet activating factor (PAF). A review of its effects, antagonists and possible future clinical implications (Part I)

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Biospecific interaction analysis using surface plasmon resonance detection applied to kinetic, binding site and concentration analysis

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10.1046/J.1432-1327.1999.00942.X

21 January 2018

Identifiers

DOI

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2 November 2019

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