Congenital hydrocephalus in genetically engineered mice (Q28506486)

24 January 2017

title

Congenital hydrocephalus in genetically engineered mice (English)

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Nucleoside diphosphate kinase 7

24 January 2017

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Unc-51-like kinase 4

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Cadherin, EGF LAG seven-pass G-type receptor 2

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Protein-O-mannose kinase

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Membrane bound O-acyltransferase domain containing 7

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Serine/threonine kinase 36

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NME/NM23 family member 5

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Deleted in primary ciliary dyskinesia

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Adenylate kinase 8

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Adenylate kinase 7

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Kinesin family member 27

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Frizzled class receptor 3

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P. Vogel

1

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author name string

R. W. Read

2

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24 January 2017

G. M. Hansen

3

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24 January 2017

B. J. Payne

4

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24 January 2017

D. Small

5

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24 January 2017

A. T. Sands

6

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24 January 2017

B. P. Zambrowicz

7

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24 January 2017

publication date

1 January 2012

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24 January 2017

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24 January 2017

volume

49

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24 January 2017

issue

1

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24 January 2017

page(s)

166–181

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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

24 January 2017

cites work

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The transcriptional landscape of the mammalian genome

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Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry

21 April 2017

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Mice deficient in the fused homolog do not exhibit phenotypes indicative of perturbed hedgehog signaling during embryonic development

21 April 2017

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Nm23-M5 mediates round and elongated spermatid survival by regulating GPX-5 levels

21 April 2017

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A high-resolution anatomical atlas of the transcriptome in the mouse embryo

21 April 2017

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Mutation of murine adenylate kinase 7 underlies a primary ciliary dyskinesia phenotype.

21 April 2017

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Msx1-deficient mice fail to form prosomere 1 derivatives, subcommissural organ, and posterior commissure and develop hydrocephalus

21 April 2017

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

21 April 2017

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Chromosomal localization of Celsr2 and Celsr3 in the mouse; Celsr3 is a candidate for the tippy (tip) lethal mutant on chromosome 9

21 April 2017

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Lysophospholipid acyltransferases and arachidonate recycling in human neutrophils

21 April 2017

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CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290

21 April 2017

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Cloning, sequencing, and characterization of the murine nm23-M5 gene during mouse spermatogenesis and spermiogenesis

21 April 2017

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Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus

21 April 2017

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Hedgehog signaling pathway and gastric cancer

21 April 2017

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Molecular cloning and genomic structure of human frizzled-3 at chromosome 8p21

21 April 2017

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https://api.crossref.org/works/10.1177/0300985811415708

Mutations in Hydin impair ciliary motility in mice

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1.

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Tissue expression patterns identify mouse cilia genes

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Loss of the serine/threonine kinase fused results in postnatal growth defects and lethality due to progressive hydrocephalus

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Cerebellar development and disease

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

A new human nm23 homologue (nm23-H5) specifically expressed in testis germinal cells

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

The characterization of human adenylate kinases 7 and 8 demonstrates differences in kinetic parameters and structural organization among the family of adenylate kinase isoenzymes

21 April 2017

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https://api.crossref.org/works/10.1177/0300985811415708

Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Subcommissural organ, cerebrospinal fluid circulation, and hydrocephalus

21 April 2017

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https://api.crossref.org/works/10.1177/0300985811415708

Msx1 disruption leads to diencephalon defects and hydrocephalus

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Male infertility, impaired sperm motility, and hydrocephalus in mice deficient in sperm-associated antigen 6

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Intraflagellar transport motors in cilia: moving along the cell's antenna

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Developmental expression profiles of Celsr (Flamingo) genes in the mouse

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Tubulin tyrosine ligase-like 1 deficiency results in chronic rhinosinusitis and abnormal development of spermatid flagella in mice

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Fused has evolved divergent roles in vertebrate Hedgehog signalling and motile ciliogenesis

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985811415708

Proteomic analysis of a eukaryotic cilium

21 April 2017

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

21 April 2017

Gene trap mutagenesis

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Adult onset hydrocephalus and situs inversus: new autosomal dominant syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Ciliary dyskinesia associated with hydrocephalus and mental retardation in a Jordanian family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

A deficiency in RFX3 causes hydrocephalus associated with abnormal differentiation of ependymal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Altered pH(i) regulation and Na(+)/HCO3(-) transporter activity in choroid plexus of cilia-defective Tg737(orpk) mutant mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

The mammalian Nm23/NDPK family: from metastasis control to cilia movement

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Hydrocephalus with hop gait (hyh): a new mutation on chromosome 7 in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

The long-term outlook for hydrocephalus in childhood. A ten-year cohort study of 155 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Hydrocephalus, a Hereditary Character in the House Mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Two Hereditary Types of Hydrocephalus in the House Mouse (Mus musculus)

21 January 2018

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https://api.crossref.org/works/10.1177%2F0300985811415708

Rhinitis/Bronchopneumonia syndrome in Irish Wolfhounds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Insights into the pathogenesis of hydrocephalus from transgenic and experimental animal models

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Communicating hydrocephalus in dogs with congenital ciliary dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Ependymal cells: biology and pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Hydrocephalus, bronchiectasis, and ciliary aplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Familial immotile-cilia syndrome in English springer spaniel dogs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Hydrocephalus and primary ciliary dyskinesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Pathogenesis of migration disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counselling

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Mouse Flamingo1/Celsr2 relates neuronal reorganization of the hypertrophic dentate granule cells after kainate injection

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Brain development in mice lacking L1-L1 homophilic adhesion

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Genetic basis of Joubert syndrome and related disorders of cerebellar development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Role of adenylate kinase type 7 expression on cilia motility: possible link in primary ciliary dyskinesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Nm23/NDP kinases in human male germ cells: role in spermiogenesis and sperm motility?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Spontaneous congenital hydrocephalus in the mutant mouse hyh. Changes in the ventricular system and the subcommissural organ

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Planarian Hh signaling regulates regeneration polarity and links Hh pathway evolution to cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Severe hydrocephalus in L1-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Opposing roles in neurite growth control by two seven-pass transmembrane cadherins

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Primary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

An epidemiologic study of environmental and genetic factors in congenital hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Development of hydrocephalus in mice expressing the G(i)-coupled GPCR Ro1 RASSL receptor in astrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Risk factors of congenital hydrocephalus: a 10 year retrospective study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Incomplete inhibition of sphingosine 1-phosphate lyase modulates immune system function yet prevents early lethality and non-lymphoid lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Ocular albinism and hypopigmentation defects in Slc24a5-/- mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Frizzled3a and Celsr2 function in the neuroepithelium to regulate migration of facial motor neurons in the developing zebrafish hindbrain

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Axonal growth and guidance defects in Frizzled3 knock-out mice: a comparison of diffusion tensor magnetic resonance imaging, neurofilament staining, and genetically directed cell labeling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Pathways of fluid drainage from the brain--morphological aspects and immunological significance in rat and man

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in the L1CAM gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Gene expression analysis of nuclear factor I-A deficient mice indicates delayed brain maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Predicting drug efficacy: knockouts model pipeline drugs of the pharmaceutical industry

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Genetics of human hydrocephalus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737(orpk) mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708

Role of the atypical cadherin Celsr3 during development of the internal capsule.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811415708