(Q41929231)

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MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulation.

scientific article published on 28 November 2014

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21 February 2020

MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulation (English)

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21 February 2020

Heinrich Sticht

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21 February 2020

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21 February 2020

Stephan C Neuhauss

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21 February 2020

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21 February 2020

Christian T Thiel

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21 February 2020

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Diana Zahnleiter

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21 February 2020

Nadine N Hauer

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21 February 2020

Kristin Kessler

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21 February 2020

Steffen Uebe

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21 February 2020

Yuya Sugano

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21 February 2020

Holger Blessing

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21 February 2020

Helmuth-Günther Dörr

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21 February 2020

Arif B Ekici

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21 February 2020

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28 November 2014

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21 February 2020

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21 February 2020

36

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21 February 2020

1

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21 February 2020

87-97

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21 February 2020

Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature

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Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway.

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Src regulates Golgi structure and KDEL receptor-dependent retrograde transport to the endoplasmic reticulum

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A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

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Regulation of microtubule-associated proteins.

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The MAP2/Tau family of microtubule-associated proteins

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Septins 2, 7 and 9 and MAP4 colocalize along the axoneme in the primary cilium and control ciliary length

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Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.

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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

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MAP4 counteracts microtubule catastrophe promotion but not tubulin-sequestering activity in intact cells.

1 reference

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The projection domain of MAP4 suppresses the microtubule-bundling activity of the microtubule-binding domain

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Phosphorylation of microtubule-associated proteins MAP2 and MAP4 by the protein kinase p110mark. Phosphorylation sites and regulation of microtubule dynamics

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CEP152 is a genome maintenance protein disrupted in Seckel syndrome

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Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome

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Hundreds of variants clustered in genomic loci and biological pathways affect human height

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Fast and accurate short read alignment with Burrows-Wheeler transform

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Autosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

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Modulation of microtubule dynamics during the cell cycle

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Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

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Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans

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Distribution of MAP-4 in cells and in adult and developing mouse tissues

1 reference

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Activation of cyclic AMP/PKA pathway inhibits bladder cancer cell invasion by targeting MAP4-dependent microtubule dynamics

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21 January 2018

CtIP Mutations Cause Seckel and Jawad Syndromes

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Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

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Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation

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ACMG practice guideline: genetic evaluation of short stature

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10.1002/HUMU.22711

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release_ys7rm7fidramfis76nk6fkv4wi

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24 November 2022

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21 February 2020

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