Kartagener Syndrome

Kartagener syndrome is an autosomal recessive disorder characterized by situs inversus, chronic sinusitis, and bronchiectasis. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and cilia in the respiratory and the reproductive tracts. Discover the latest research on Kartagener syndrome here.

September 30, 2020
Open Access

A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

Disease Models & Mechanisms
Zakia AbdelhamedRolf W Stottmann
January 16, 2021
Open Access

Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia

ERJ Open Research
Alex Gileles-HillelOded Breuer
October 20, 2020
Open Access

Variants in RABL2A causing male infertility and ciliopathy

Human Molecular Genetics
Xinbao DingJohn C Schimenti
January 7, 2021
Open Access

Risk of Pneumonia Associated with Inhaled Corticosteroid in Patients with Chronic Obstructive Pulmonary Disease: A Korean Population-Based Study

International Journal of Chronic Obstructive Pulmonary Disease
Ji-Ho LeeWon-Yeon Lee
November 27, 2020

Understanding primary ciliary dyskinesia and other ciliopathies

The Journal of Pediatrics
Amjad Horani, Thomas Ferkol
October 13, 2020
Open Access

Are gain values significantly altered by manual data selection when performing the video Head Impulse Test (v-HIT) on all six semicircular canals with two different v-HIT systems

Journal of Vestibular Research : Equilibrium & Orientation
Emil Riis AbrahamsenDan Dupont Hougaard
January 23, 2021

Topological data analysis reveals genotype-phenotype relationships in primary ciliary dyskinesia.

The European Respiratory Journal
Amelia ShoemarkJane S Lucas
October 1, 2020

PCD Detect: enhancing ciliary features through image averaging and classification

American Journal of Physiology. Lung Cellular and Molecular Physiology
Amelia ShoemarkThomas Burgoyne
November 25, 2020
Preprint
Open Access

Cilia-independent requirements for Ccdc103 promoting proliferation and migration of myeloid cells

BioRxiv : the Preprint Server for Biology
L. FalkenbergJoshua Waxman
December 22, 2020
Preprint
Open Access

SARS-CoV-2 infections in people with PCD: neither frequent, nor particularly severe

MedRxiv : the Preprint Server for Health Sciences
E. S. L. PedersenClaudia E Kuehni
January 5, 2021
Open Access

In vivo Evaluation of Mucociliary Clearance in Mice.

Journal of Visualized Experiments : JoVE
Kyle S Feldman, Maliha Zahid
January 7, 2021

The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient

Journal of Assisted Reproduction and Genetics
Yaqian LiYing Shen
October 8, 2020

Lung transplantation for Kartagener syndrome: technical aspects and morphological adaptation of the transplanted lungs

General Thoracic and Cardiovascular Surgery
Haruchika YamamotoShinichi Toyooka
November 25, 2020
Review

Pulmonary Manifestations of Genetic Disorders in Children

Pediatric Clinics of North America
Beth A Pletcher, Nelson L Turcios

Sign up to follow this feed and discover related papers.

Related Feeds

22q11 Deletion Syndrome

22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a congenital disorder caused as a result of a partial deletion of chromosome 22. Here is the latest research.

Alagille Syndrome

Alagille syndrome is a multi-system genetic disorder that can affect the liver, heart, and other parts of the body. It’s characterization includes heart problems, liver damage, jaundice, and xanthomas. Here is the latest research.

Aneurysm

Aneurysms are outward distensions or bulges that occurs in a weakened wall of blood vessels. Discover the latest research on aneurysms here.

Antiarrhythmic Agents: Mechanisms of Action

Understanding the mechanism of action of antiarrhythmic agents is essential in developing new medications as treatment of cardiac arrhythmias is currently limited by the reduced availability of safe and effective drugs. Discover the latest research on Antiarrhythmic Agents: Mechanism of Action here.

Aortic Aneurysm

An aortic aneurysm is the weakening and bulging of the blood vessel wall in the aorta. This causes dilatation of the aorta, which is usually asymptomatic but carries the risk of rupture and hemorrhage. Find the latest research on aortic aneurysms here.

Aortic Coarctation

Aortic coarctation is a congenital condition characterized by narrowing of the aorta. Discover the latest research on this disease here.

ApoE Phenotypes

Apolipoprotein E (APOE) is a protein involved in fat metabolism and associated with the pathogenesis of Alzheimer's disease and cardiovascular disease. Here is the latest research on APOE phenotypes.

Arrhythmia

Arrhythmias are abnormalities in heart rhythms, which can be either too fast or too slow. They can result from abnormalities of the initiation of an impulse or impulse conduction or a combination of both. Here is the latest research on arrhythmias.

Arrhythmogenic Right Ventricular Dysplasia

Arrhythmogenic right ventricular dysplasia is a congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the right ventricle wall and loss of myocardial cells. Primary injuries usually are at the free wall of the right ventricular and right atria resulting in ventricular and supraventricular arrhythmias. Discover the latest research on arrhythmogenic right ventricular dysplasia here.

Arterial-Venous in Development & Disease

Arterial-venous development may play a crucial role in cardiovascular diseases. Here is the latest research.

© 2021 Meta ULC. All rights reserved
/feed-previews/kartagener-syndrome/5b295c8b-52d0-4924-afb9-3381ebafb442