(Q38309287)

2 September 2017

title

Patient mutations in doublecortin define a repeated tubulin-binding domain (English)

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2 September 2017

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Taylor KR

1

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2 September 2017

Holzer AK

2

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2 September 2017

Bazan JF

3

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2 September 2017

Walsh CA

4

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2 September 2017

Gleeson JG

5

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2 September 2017

language of work or name

English

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publication date

1 November 2000

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Journal of Biological Chemistry

2 September 2017

published in

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2 September 2017

volume

275

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2 September 2017

issue

44

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2 September 2017

page(s)

34442-34450

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

2 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Epilepsy and anomalies of neuronal migration: MRI and clinical aspects

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Doublecortin, a stabilizer of microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Turbidimetric studies of the in vitro assembly and disassembly of porcine neurotubules

21 January 2018

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Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

21 January 2018

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Analysis of the microtubule-binding domain of MAP-2.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

A three-domain structure of kinesin heavy chain revealed by DNA sequence and microtubule binding analyses

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

The microtubule binding domain of microtubule-associated protein MAP1B contains a repeated sequence motif unrelated to that of MAP2 and tau

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Identification of a Microtubule-binding Domain in a Cytoplasmic Dynein Heavy Chain

21 January 2018

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Exploring the microtubule-binding region of bovine microtubule-associated protein-2 (MAP-2): cDNA sequencing, bacterial expression, and site-directed mutagenesis

21 January 2018

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The microtubule binding domain of tau protein.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Functional interactions between the proline-rich and repeat regions of tau enhance microtubule binding and assembly

21 January 2018

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Organization and energy-dependent growth of microtubules in cells

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Solution structure of the Ras-binding domain of c-Raf-1 and identification of its Ras interaction surface

21 January 2018

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The 2.2 A crystal structure of the Ras-binding domain of the serine/threonine kinase c-Raf1 in complex with Rap1A and a GTP analogue

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Three-dimensional structure of the Ras-interacting domain of RalGDS

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Structure of the Ras-binding domain of RalGEF and implications for Ras binding and signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Doublecortin mutations cluster in evolutionarily conserved functional domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Mutations in the GAP-related domain impair the ability of neurofibromin to associate with microtubules.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M007078200

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

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Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Missense tau mutations identified in FTDP-17 have a small effect on tau-microtubule interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

Characterization of mutations in the gene doublecortin in patients with double cortex syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007078200

21 January 2018

Identifiers

DOI

10.1074/JBC.M007078200

1 reference

2 September 2017

1 reference