Results 111 to 120 of about 6,532,899 (237)

Phenylacetic acid metabolic genes are associated with Mycobacteroides abscessus dominant circulating clone 1

open access: yesMicrobiology Spectrum
Mycobacteroides abscessus (MAB) causes lung infections in people with cystic fibrosis (pwCF), and infecting strains show significant genetic variability both between and within individuals. MAB isolates can be divided into dominant clonal clusters (DCCs)
Brittany N. Ross   +2 more
doaj   +1 more source

Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory mutants of the tinman-related genes, XNkx2-3 and XNkx2-5.

open access: yesDevelopmental Biology, 1998
In Drosophila, the tinman gene is absolutely required for development of the dorsal vessel, the insect equivalent of the heart. In vertebrates, the tinman gene is represented by a small family of tinman-related sequences, some of which are expressed ...
M. Grow, P. Krieg
semanticscholar   +1 more source

Gastric pseudoaneurysm in the setting of Loey’s Dietz Syndrome [PDF]

open access: yes, 2012
Loey’s Dietz syndrome is a disorder of connective tissue caused by a mutation in the genes that encode transforming growth factor (TGF) beta receptor 1 and 2.
Johston, Troy Alan, Likes, Maggie L.
core   +1 more source

Genetic regulation of pituitary gland development in human and mouse [PDF]

open access: yes, 2009
Normal hypothalamopituitary development is closely related to that of the forebrain and is dependent upon a complex genetic cascade of transcription factors and signaling molecules that may be either intrinsic or extrinsic to the developing Rathke’s ...
Aarskog   +321 more
core   +2 more sources

Insight into Dominant Cellulolytic Bacteria from Two Biogas Digesters and Their Glycoside Hydrolase Genes.

open access: yesPLoS ONE, 2015
Diverse cellulolytic bacteria are essential for maintaining high lignocellulose degradation ability in biogas digesters. However, little was known about functional genes and gene clusters of dominant cellulolytic bacteria in biogas digesters. This is the
Yongjun Wei   +9 more
doaj   +1 more source

Identification of a New Chromosomal Region Involved in the Genetic Control of Resistance to Anthracnose in Common Bean

open access: yesThe Plant Genome, 2015
Anthracnose caused by (Sacc. & Magnus) Lams.-Scrib. is a major disease affecting common bean ( L.) crops worldwide. Response to five isolates, classified as races 3, 6, 7, 38, and 73, were analyzed in 156 F families derived from the cross between line ...
Noemí Trabanco   +2 more
doaj   +1 more source

The promoters of human cell cycle genes integrate signals from two tumor suppressive pathways during cellular transformation [PDF]

open access: yes, 2005
Deciphering regulatory events that drive malignant transformation represents a major challenge for systems biology. Here we analyzed genome-wide transcription profiling of an in-vitro transformation process.
Assif Yitzhaky   +17 more
core   +3 more sources

The Multigeneic _Rhg1_ Locus: A Model For The Effects on Root Development, Nematode Resistance and Recombination Suppression. [PDF]

open access: yes, 2008
Soybean (Glycine max L. Merr.) resistance to populations (HgType) of _Heterodera glycines I._, the soybean cyst nematode (SCN), requires a functional allele at rhg1. An apoptosis-like response in the giant cells formed around the nematode results 24-48 h
Ali Srour   +3 more
core   +2 more sources

Quantitative analysis of regulatory flexibility under changing environmental conditions [PDF]

open access: yes, 2010
The circadian clock controls 24-h rhythms in many biological processes, allowing appropriate timing of biological rhythms relative to dawn and dusk. Known clock circuits include multiple, interlocked feedback loops.
Adrian W Thomson   +12 more
core   +4 more sources

Autosomal dominant Alport syndrome linked to the type IV collage alpha 3 and alpha 4 genes (COL4A3 and COL4A4).

open access: yesNephrology, Dialysis and Transplantation, 1997
BACKGROUND Alport syndrome is a hereditary nephritis that may lead to end-stage renal disease (ESRD) in young adult life and is often associated with sensorineural deafness and/or ocular abnormalities.
J. Jefferson   +6 more
semanticscholar   +1 more source

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