MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulation. (Q41929231)

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scientific article published on 28 November 2014

Language	Label	Description	Also known as
English	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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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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

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Europe PubMed Central

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14 October 2017

Heinrich Sticht

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Christian T Thiel

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Christian T Thiel

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author name string

Diana Zahnleiter

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Europe PubMed Central

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14 October 2017

Nadine N Hauer

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Kristin Kessler

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14 October 2017

Steffen Uebe

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14 October 2017

Yuya Sugano

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14 October 2017

Stephan C F Neuhauss

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14 October 2017

Andreas Giessl

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14 October 2017

Arif B Ekici

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14 October 2017

Holger Blessing

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14 October 2017

Helmuth-Günther Dörr

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14 October 2017

publication date

28 November 2014

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14 October 2017

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14 October 2017

36

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14 October 2017

87-97

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14 October 2017

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

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Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity

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

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Sequence and structure-based prediction of eukaryotic protein phosphorylation sites

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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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Majewski osteodysplastic primordial dwarfism type II (MOPD II): natural history and clinical findings.

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Topography of glycosylation in the rough endoplasmic reticulum and Golgi apparatus

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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.

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Predominant regulators of tubulin monomer-polymer partitioning and their implication for cell polarization

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PhosphoSitePlus: a comprehensive resource for investigating the structure and function of experimentally determined post-translational modifications in man and mouse

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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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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

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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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CtIP Mutations Cause Seckel and Jawad Syndromes

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Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

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MAP4 and CLASP1 operate as a safety mechanism to maintain a stable spindle position in mitosis

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

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POC1A truncation mutation causes a ciliopathy in humans characterized by primordial dwarfism

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Concerted effort of centrosomal and Golgi-derived microtubules is required for proper Golgi complex assembly but not for maintenance

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Identifiers

10.1002/HUMU.22711

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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