Results 101 to 110 of about 8,141 (357)

Overlapping and distinct expression domains of Zic2 and Zic3 during mouse gastrulation

open access: yes, 2016
The Zic genes are the vertebrate homologues of the Drosophila Odd-paired gene. Mutations in two of these genes are associated with human congenital genetic disorders.
Arkell, Ruth   +6 more
core   +1 more source

PICADAR: a diagnostic predictive tool for primary ciliary dyskinesia [PDF]

open access: yes, 2016
Symptoms of primary ciliary dyskinesia (PCD) are nonspecific and guidance on whom to refer for testing is limited. Diagnostic tests for PCD are highly specialised, requiring expensive equipment and experienced PCD scientists. This study aims to develop a
Behan, Laura   +10 more
core   +1 more source

A Proof‐of‐Concept Assessment of a Novel Wearable Eyelid Muscle Device: A Pre‐Clinical Animal Cadaver Study for Eyelid Closure Restoration

open access: yesAdvanced Robotics Research, EarlyView.
This article introduces a soft wearable eyelid sling device incorporating a hydraulic soft artificial muscle (SAM) for achieving complete closure of an eyelid. The SAM is driven by a cam mechanism that provides a displacement profile closely matched with those of a healthy eyelid.
Patrick Pruscino   +7 more
wiley   +1 more source

The inferior caval vein draining into the left atrial cavity : a rare case [PDF]

open access: yes, 2011
The inferior vena cava (IVC) draining into the left atrium (LA) is exceedingly rare in the setting of the usual atrial arrangement (situs solitus).
McCarthy, Karen   +4 more
core  

Whole exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association [PDF]

open access: yes, 2014
Congenital abnormalities of the kidney and urinary tract (CAKUT) account for approximately half of children with chronic kidney disease and they are the most frequent cause of end-stage renal disease in children in the US.
Bartels, Enrika   +34 more
core   +2 more sources

NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy

open access: yesGenome Medicine
NODAL signaling plays a critical role in embryonic patterning and heart development in vertebrates. Genetic variants resulting in perturbations of the TGF-β/NODAL signaling pathway have reproducibly been shown to cause laterality defects in humans.
Z. Dardas   +17 more
semanticscholar   +1 more source

Gait Analysis of Pak Biawak: A Necrobot Lizard Built using the Skeleton of an Asian Water Monitor (Varanus Salvator)

open access: yesAdvanced Robotics Research, EarlyView.
Pak Biawak, a necrobot, embodies an unusual fusion of biology and robotics. Designed to repurpose natural structures after death, it challenges conventional boundaries between nature and engineering. Its movements are precise yet unsettling, raising questions about sustainability, ethics, and the untapped potential of biointegrated machines.
Leo Foulds   +2 more
wiley   +1 more source

Electrophysiology Study for Complex Supraventricular Tachycardia in Congenital Heart Disease Patients With Single‐Ventricle Physiology

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2016
BackgroundSupraventricular tachycardia (SVT) is common in complex congenital heart disease (CCHD) patients with single‐ventricle physiology and may cause hemodynamic deterioration.
Shuenn‐Nan Chiu   +5 more
doaj   +1 more source

Situs InversusTotalis with Malposition of Caecum and Ascending colon [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2016
Situs Inversus Totalis (SIT) is an inversion anomaly involving the position of abdominal and thoracic viscera with respect to the midline. The medical and surgical management of these patients are technically more challenging because of the mirror ...
Vidya Gunasekaran   +2 more
doaj   +1 more source

Coronary steal syndrome after coronary artery bypass for anomalous aortic origin of a coronary artery. [PDF]

open access: yes, 2009
Anomalous aortic origin of a coronary artery found in a symptomatic 9-year-old boy was initially treated with coronary artery bypass grafting using a left internal mammary artery anastomoses to the left anterior descending coronary artery, but resulted ...
Jacobs, Marshall L   +3 more
core   +2 more sources

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