DYX1C1 is required for axonemal dynein assembly and ciliary motility (Q24310331)

25 June 2017

title

DYX1C1 is required for axonemal dynein assembly and ciliary motility (English)

1 reference

Dynein axonemal assembly factor 4

25 June 2017

main subject

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inner dynein arm assembly

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Chaperonin containing Tcp1, subunit 3 (gamma)

1 reference

Dynein axonemal assembly factor 4

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Chaperonin containing Tcp1, subunit 8 (theta)

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Chaperonin containing Tcp1, subunit 4 (delta)

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Chaperonin containing Tcp1, subunit 5 (epsilon)

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36

Vincent Plagnol

Vincent

Plagnol

1 reference

25 June 2017

Adam J Shapiro

Adam J

Shapiro

27

1 reference

19 October 2023

Miriam Schmidts

37

Miriam

Schmidts

1 reference

19 October 2023

Jane S Lucas

34

Jane S

Lucas

1 reference

19 October 2023

Rebecca D Burdine

45

Rebecca D

Burdine

1 reference

19 October 2023

Brett Shook

7

Brett

Shook

1 reference

19 October 2023

Rim Hjeij

16

Rim

Hjeij

1 reference

19 October 2023

Richard Francis

4

Richard

Francis

1 reference

19 October 2023

12

Claudius Werner

Claudius

Werner

1 reference

25 June 2017

11

Heike Olbrich

Heike

Olbrich

1 reference

25 June 2017

47

Heymut Omran

Heymut

Omran

1 reference

25 June 2017

41

Maimoona A Zariwala

Maimoona A

Zariwala

1 reference

25 June 2017

Aarti Tarkar

1

Aarti

Tarkar

1 reference

25 June 2017

Niki T Loges

2

Niki T

Loges

1 reference

25 June 2017

Christopher E Slagle

3

Christopher E

Slagle

1 reference

25 June 2017

Gerard W Dougherty

5

Gerard W

Dougherty

1 reference

25 June 2017

Joel V Tamayo

6

Joel V

Tamayo

1 reference

25 June 2017

Marie Cantino

8

Marie

Cantino

1 reference

25 June 2017

Daniel Schwartz

9

Daniel

Schwartz

1 reference

25 June 2017

Charlotte Jahnke

10

Charlotte

Jahnke

1 reference

25 June 2017

Johanna Raidt

13

Johanna

Raidt

1 reference

25 June 2017

Petra Pennekamp

14

Petra

Pennekamp

1 reference

25 June 2017

Marouan Abouhamed

15

Marouan

Abouhamed

1 reference

25 June 2017

Gabriele Köhler

17

Gabriele

Köhler

1 reference

25 June 2017

Matthias Griese

18

Matthias

Griese

1 reference

25 June 2017

You Li

19

You

Li

1 reference

25 June 2017

Kristi Lemke

20

Kristi

Lemke

1 reference

25 June 2017

Nikolas Klena

21

Nikolas

Klena

1 reference

25 June 2017

Xiaoqin Liu

22

Xiaoqin

Liu

1 reference

25 June 2017

George Gabriel

23

George

Gabriel

1 reference

25 June 2017

Kimimasa Tobita

24

Kimimasa

Tobita

1 reference

25 June 2017

Martine Jaspers

25

Martine

Jaspers

1 reference

25 June 2017

Lucy C Morgan

26

Lucy C

Morgan

1 reference

25 June 2017

Stef J F Letteboer

28

Stef J F

Letteboer

1 reference

25 June 2017

Dorus A Mans

29

Dorus A

Mans

1 reference

25 June 2017

Johnny L Carson

30

Johnny L

Carson

1 reference

25 June 2017

Margaret W Leigh

31

Margaret W

Leigh

1 reference

25 June 2017

Whitney E Wolf

32

Whitney E

Wolf

1 reference

25 June 2017

Serafine Chen

33

Serafine

Chen

1 reference

25 June 2017

Alexandros Onoufriadis

35

Alexandros

Onoufriadis

1 reference

25 June 2017

Cecilia W Lo

42

Cecilia W

Lo

1 reference

25 June 2017

Hannah M Mitchison

43

Hannah M

Mitchison

1 reference

25 June 2017

Michael R Knowles

44

Michael R

Knowles

1 reference

25 June 2017

Joseph J Loturco

46

Joseph J

Loturco

1 reference

25 June 2017

Karsten Boldt

38

Karsten

Boldt

1 reference

25 June 2017

UK10K

39

1 reference

25 June 2017

Ronald Roepman

40

Ronald

Roepman

1 reference

25 June 2017

language of work or name

English

0 references

publication date

21 July 2013

1 reference

25 June 2017

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25 June 2017

volume

45

1 reference

25 June 2017

issue

9

1 reference

25 June 2017

page(s)

995-1003

1 reference

describes a project that uses

25 June 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4000444/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

DYX1C1 functions in neuronal migration in developing neocortex

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Characterization of an axonemal dynein heavy chain expressed early in airway epithelial ciliogenesis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Congenital hydrocephalus in genetically engineered mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Association of short-term memory with a variant within DYX1C1 in developmental dyslexia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

The murine Dnali1 gene encodes a flagellar protein that interacts with the cytoplasmic dynein heavy chain 1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

19 March 2017

1 reference

Crossref

https://api.crossref.org/works/10.1038/NG.2707

Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists

22 April 2017

1 reference

Crossref

https://api.crossref.org/works/10.1038/NG.2707

When cilia go bad: cilia defects and ciliopathies

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Detection of messenger RNA by in situ hybridization to tissue sections and whole mounts

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

A robust model for read count data in exome sequencing experiments and implications for copy number variant calling

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Exploring the transcriptome of ciliated cells using in silico dissection of human tissues

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

CCTalpha and CCTdelta chaperonin subunits are essential and required for cilia assembly and maintenance in Tetrahymena

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Genetic defects in ciliary structure and function

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

A southpaw joins the roster: the role of the zebrafish nodal-related gene southpaw in cardiac LR asymmetry

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

All-digital image capture and whole-field analysis of ciliary beat frequency

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Restricted expression of cardiac myosin genes reveals regulated aspects of heart tube assembly in zebrafish.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

fork head domain genes in zebrafish

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Network of tangential pathways for neuronal migration in adult mammalian brain

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Anterior and posterior compartments in the proboscis of Drosophila

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

A novel role for DYX1C1, a chaperone protein for both Hsp70 and Hsp90, in breast cancer

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Interaction of U-box-type ubiquitin-protein ligases (E3s) with molecular chaperones

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Abnormal nodal flow precedes situs inversus in iv and inv mice

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Conservation of PDX-1 structure, function, and expression in zebrafish

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4000444

Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation

29 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/23872636

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The EGF-CFC protein one-eyed pinhead is essential for nodal signaling

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2707

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.2707

1 reference

Dimensions Publication ID

25 June 2017

1025255428

0 references

Fatcat ID

release_xng4u5lxdrbirczuuevbm4ppcy

0 references

OpenCitations bibliographic resource ID

1629810

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1629810

1 reference