Lateralization defects and ciliary dyskinesia: lessons from algae (Q35076952)

6 August 2017

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title

Lateralization defects and ciliary dyskinesia: lessons from algae (English)

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6 August 2017

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2

Heymut Omran

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6 August 2017

Loubna El Zein

1

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6 August 2017

Patrice Bouvagnet

series ordinal

3

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6 August 2017

publication date

1 March 2003

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6 August 2017

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6 August 2017

volume

19

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6 August 2017

issue

3

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6 August 2017

page(s)

162-167

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Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes

6 August 2017

cites work

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7 January 2021

Model for the motor component of dynein heavy chain based on homology to the AAA family of oligomeric ATPases

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7 January 2021

An extended microtubule-binding structure within the dynein motor domain

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7 January 2021

Light chain 1 from the Chlamydomonas outer dynein arm is a leucine-rich repeat protein associated with the motor domain of the gamma heavy chain

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7 January 2021

Flagellar assembly in two hundred and fifty easy-to-follow steps

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7 January 2021

Expression of primary cilia in mammalian cells

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7 January 2021

Assembly and motility of eukaryotic cilia and flagella. Lessons from Chlamydomonas reinhardtii

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7 January 2021

The 78,000 M(r) intermediate chain of Chlamydomonas outer arm dynein isa WD-repeat protein required for arm assembly

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7 January 2021

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

1 reference

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7 January 2021

Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)

1 reference

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7 January 2021

Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene

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7 January 2021

The sup-pf-2 mutations of Chlamydomonas alter the activity of the outer dynein arms by modification of the gamma-dynein heavy chain

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7 January 2021

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

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7 January 2021

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

1 reference

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7 January 2021

Mutations at twelve independent loci result in absence of outer dynein arms in Chylamydomonas reinhardtii

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7 January 2021

The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia

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7 January 2021

Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia

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7 January 2021

Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia

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7 January 2021

The Tctex1/Tctex2 class of dynein light chains. Dimerization, differential expression, and interaction with the LC8 protein family

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7 January 2021

DYNEINS: molecular structure and cellular function

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7 January 2021

Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency

1 reference

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7 January 2021

Casein kinase I is anchored on axonemal doublet microtubules and regulates flagellar dynein phosphorylation and activity

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7 January 2021

Radial spokes of Chlamydomonas flagella: genetic analysis of assembly and function

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7 January 2021

Central-pair microtubular complex of Chlamydomonas flagella: polypeptide composition as revealed by analysis of mutants

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7 January 2021

Isolation and expression of the human hPF20 gene orthologous to Chlamydomonas PF20: evaluation as a candidate for axonemal defects of respiratory cilia and sperm flagella.

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7 January 2021

Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice

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7 January 2021

Conserved function for embryonic nodal cilia.

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7 January 2021

Abnormal nodal flow precedes situs inversus in iv and inv mice

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7 January 2021

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

1 reference

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7 January 2021

Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis

1 reference

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7 January 2021

Determination of left–right patterning of the mouse embryo by artificial nodal flow

1 reference

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7 January 2021

X-linked situs abnormalities result from mutations in ZIC3

1 reference

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7 January 2021

X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3.

1 reference

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7 January 2021

10.1016/S0168-9525(03)00026-X

Identifiers

DOI

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6 August 2017

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