Results 91 to 100 of about 2,079 (225)

A knock‐in allele of Hand2 expressing Dre recombinase

open access: yesgenesis, Volume 62, Issue 3, June 2024.
Summary HAND2 is a basic helix–loop–helix transcription factor with diverse functions during development. To facilitate the investigation of genetic and functional diversity among Hand2‐expressing cells in the mouse, we have generated Hand2Dre, a knock‐in allele expressing Dre recombinase. To avoid disrupting Hand2 function, the Dre cDNA is inserted at
Nicholas W. Plummer   +2 more
wiley   +1 more source

Pentalogy of cantrell [PDF]

open access: yes, 2019
[No abstract available ...
Ahmed B.   +3 more
core   +1 more source

Ectopia cordis with endocardial cushion defect: Prenatal ultrasonographic diagnosis with autopsy correlation

open access: yesAnnals of Pediatric Cardiology, 2010
The prenatal ultrasonographic diagnosis of ectopia cordis associated with a complex intra-cardiac defect (common atrium, common atrioventricular valve with single ventricle) is illustrated in a 32-week gestation fetus.
Balakumar K, Misha K
doaj  

Prenatal Diagnosis of Cantrell’s Pentalogy Associated with Agenesis of Left Limb in a Twin Pregnancy

open access: yesCase Reports in Obstetrics and Gynecology, 2014
Pentalogy of Cantrell is a rare malformation described in the literature. We report a case of pentalogy of Cantrell associated with left limb deficiency in a twin pregnancy. The fetus with multiple anomalies revealed kyphosis, ectopia cordis, and a large
Yigit Cakiroglu   +5 more
doaj   +1 more source

Cervical ectopia cordis in a calf: a case report

open access: yesVeterinární Medicína, 2016
A female Holstein Friesian calf with inferior cervical ectopia cordis was followed from the 16th day of age until euthanasia at the age of three months. The heart was located in the lower cervical region and was covered with skin.
J. Jezek   +3 more
doaj   +1 more source

Ectopia Cordis in a 35 Day Old Human Embryo [PDF]

open access: yes, 1958
One of the major, though fortunately rare, abnormalities of human intrauterine development is a condition known as ectopia cordis. It was first described by the Swiss poet, physician and naturalist Haller in 1706.
Enzmann, E. V.   +2 more
core   +1 more source

Fetal cardiac screening: 1st trimester and beyond

open access: yesPrenatal Diagnosis, Volume 44, Issue 6-7, Page 679-687, June 2024.
Abstract Congenital heart defects (CHD) are the most common birth defect and a leading cause of infant morbidity and mortality. CHD often occurs in low‐risk pregnant patients, which underscores the importance of routine fetal cardiac screening at the time of the 2nd trimester ultrasound.
Lindsay R. Freud, Lynn L. Simpson
wiley   +1 more source

Body Stalk Syndrome: A Curiosity [PDF]

open access: yes, 2014
Limb body wall complex (LBWC) /Body stalk syndrome anomaly refers to a rare complicated polymalformative fetal malformation syndrome of uncertain etiology firstly described by Van Allen et al in 1987.
Anilkumar S.   +3 more
core  

Asociación de ectopia cordis con pentalogía de Cantrell a partir de variantes en el gen ALDH1A2. [PDF]

open access: yes, 2022
Objetivo: Identificar la relación de variantes en el gen ALDH1A2 con la ectopia cordis descrita en los pacientes con pentalogía de Cantrell. Materiales y métodos: Según la declaración PRISMA, se realizó una búsqueda sistematizada de la literatura en ...
Jiménez-Müller, Hana   +2 more
core   +1 more source

Copy number variations: The potential association genetic cause in severe cardiovascular diseases with unknown aetiology

open access: yesJournal of Cellular and Molecular Medicine, Volume 28, Issue 12, June 2024.
Abstract Cardiovascular diseases (CVDs) are the leading cause of mortality worldwide. While both genetic and environmental factors significantly contribute to the pathogenesis of CVDs, recent advancements in genetic technology have further emphasized the significance of genetic factors in CVDs.
Niloofar Naderi   +3 more
wiley   +1 more source

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