Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia. - Wikidata - thesis-toulmin - TriplyDB

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

http://www.wikidata.org/entity/Q34565864

about

Otitis media in a new mouse model for CHARGE syndrome with a deletion in the Chd7 gene Light, polarizing, and transmission electron microscopy: three methods for the evaluation of sperm quality.Ciliary ultrastructure in patients with chronic rhinosinusitis and primary ciliary dyskinesia.Live birth after Laser Assisted Viability Assessment (LAVA) to detect pentoxifylline resistant ejaculated immotile spermatozoa during ICSI in a couple with male Kartagener's syndrome.The Contemporary Use of Electron Microscopy in the Diagnosis of Ciliary Disorders and Sperm Centriolar Abnormalities

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Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

http://www.wikidata.org/entity/Q34565864

description

2006 nî lūn-bûn

@nan

2006 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հունվարին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

@zh-hant

2006年論文

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2006年論文

@zh-mo

2006年論文

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2006年论文

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name

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@ast

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@en

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@nl

type

label

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@ast

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@en

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@nl

prefLabel

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@ast

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@en

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@nl

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P1433

Upsala Journal of Medical Sciences

P1476

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

@en

P2093

Andrejs Ivanovs

http://www.w3.org/2001/XMLSchema#string

Eyman B Shebani

http://www.w3.org/2001/XMLSchema#string

Godfried M Roomans

http://www.w3.org/2001/XMLSchema#string

Marie Johannesson

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P2860

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

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

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

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

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

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

Localization of calmodulin and dynein light chain LC8 in flagellar radial spokes

Primary ciliary dyskinesia: diagnosis and standards of care

Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients

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

P304

155-168

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scholarly article

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10.3109/2000-1967-010

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1

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111

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2006-01-01T00:00:00Z

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7226316

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16553254

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