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

From Wikidata

Jump to navigation Jump to search

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

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

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

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Heinrich Sticht

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

12

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Stephan C Neuhauss

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Christian T Thiel

13

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

author name string

Diana Zahnleiter

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Nadine N Hauer

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Kristin Kessler

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Steffen Uebe

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Yuya Sugano

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Holger Blessing

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Helmuth-Günther Dörr

11

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Arif B Ekici

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

publication date

28 November 2014

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

36

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

87-97

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

A method and server for predicting damaging missense mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Novel CENPJ mutation causes Seckel syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Sequence and structure-based prediction of eukaryotic protein phosphorylation sites

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Regulation of microtubule-associated proteins.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

The MAP2/Tau family of microtubule-associated proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

A framework for variation discovery and genotyping using next-generation DNA sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Height matters-from monogenic disorders to normal variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

A systematic review and meta-analysis to revise the Fenton growth chart for preterm infants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

An integrated map of genetic variation from 1,092 human genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Topography of glycosylation in the rough endoplasmic reticulum and Golgi apparatus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

CEP152 is a genome maintenance protein disrupted in Seckel syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Modulation of microtubule dynamics during the cell cycle

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

CtIP Mutations Cause Seckel and Jawad Syndromes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Integrative genomics viewer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

NIH Image to ImageJ: 25 years of image analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

ACMG practice guideline: genetic evaluation of short stature

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

HomozygosityMapper--an interactive approach to homozygosity mapping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

NEK1 mutations cause short-rib polydactyly syndrome type majewski

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Compensation for a gene trap mutation in the murine microtubule-associated protein 4 locus by alternative polyadenylation and alternative splicing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Nosology and classification of genetic skeletal disorders: 2010 revision.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Structural evidence for cooperative microtubule stabilization by Taxol and the endogenous dynamics regulator MAP4.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Rare copy number variants are a common cause of short stature

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

21 January 2018

Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: report of a novel mutation of the PCNT gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic analysis of short children with apparent growth hormone insensitivity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22711

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.22711

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

release_ys7rm7fidramfis76nk6fkv4wi

1 reference

https://api.fatcat.wiki/v0/release/ys7rm7fidramfis76nk6fkv4wi

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25323976%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41929231&oldid=1843589371"