Genetics and genomics of congenital heart disease

S Zaidi, M Brueckner - Circulation research, 2017 - Am Heart Assoc
Congenital heart disease is the most common birth defect, and because of major advances
in medical and surgical management, there are now more adults living with congenital heart …

Drosophila tools and assays for the study of human diseases

B Ugur, K Chen, HJ Bellen - Disease models & mechanisms, 2016 - journals.biologists.com
Many of the internal organ systems of Drosophila melanogaster are functionally analogous
to those in vertebrates, including humans. Although humans and flies differ greatly in terms …

Drosophila as a Genetic Model for Hematopoiesis

U Banerjee, JR Girard, LM Goins, CM Spratford - Genetics, 2019 - academic.oup.com
In this FlyBook chapter, we present a survey of the current literature on the development of
the hematopoietic system in Drosophila. The Drosophila blood system consists entirely of …

Whole genome analysis of a schistosomiasis-transmitting freshwater snail

CM Adema, LDW Hillier, CS Jones, ES Loker… - Nature …, 2017 - nature.com
Biomphalaria snails are instrumental in transmission of the human blood fluke Schistosoma
mansoni. With the World Health Organization's goal to eliminate schistosomiasis as a global …

[图书][B] The regulatory genome: gene regulatory networks in development and evolution

EH Davidson - 2010 - books.google.com
Gene regulatory networks are the most complex, extensive control systems found in nature.
The interaction between biology and evolution has been the subject of great interest in …

TGFβ2 knockout mice have multiple developmental defects that are non-overlapping with other TGFβ knockout phenotypes

LP Sanford, I Ormsby, ACG Groot, H Sariola… - …, 1997 - journals.biologists.com
The growth and differentiation factor transforming growth factor-β2 (TGFβ2) is thought to play
important roles in multiple developmental processes. Targeted disruption of the TGF β2 …

Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5

JJ Schott, DW Benson, CT Basson, W Pease… - Science, 1998 - science.org
Mutations in the gene encoding the homeobox transcription factor NKX2-5 were found to
cause nonsyndromic, human congenital heart disease. A dominant disease locus …

Gene regulatory networks in the evolution and development of the heart

EN Olson - Science, 2006 - science.org
The heart, an ancient organ and the first to form and function during embryogenesis, evolved
by the addition of new structures and functions to a primitive pump. Heart development is …

Transcriptional control of muscle development by myocyte enhancer factor-2 (MEF2) proteins

BL Black, EN Olson - Annual review of cell and developmental …, 1998 - annualreviews.org
▪ Abstract Metazoans contain multiple types of muscle cells that share several common
properties, including contractility, excitability, and expression of overlapping sets of muscle …

Integrin-mediated signal transduction linked to Ras pathway by GRB2 binding to focal adhesion kinase

DD Schlaepfer, SK Hanks, T Hunter, P Geer - Nature, 1994 - nature.com
The cytoplasmic focal adhesion protein-tyrosine kinase (FAK) localizes with surface integrin
receptors at sites where cells attach to the extracellular matrix. Increased FAK tyrosine …