Results 51 to 60 of about 4,657,667 (177)

Molecular genetics of suicide

open access: yesZdravniški Vestnik, 2006
Background: Suicide is a complex phenomenon that is triggered by environmental factors, and probably partially also by genetic code. Genetic studies performed on suicide brain contributed interesting findings on serotonergic, dopaminergic and ...
Alja Videtič, Galina Pungerčič
doaj  

ROS Regulate Caspase-Dependent Cell Delamination without Apoptosis in the Drosophila Pupal Notum

open access: yesiScience, 2020
Summary: Thorax fusion occurs in the midline of the Drosophila pupal notum and involves epithelial cell delamination requiring apoptotic signaling. By genetic screening, we found that NADPH oxidases (Nox and Duox) associated with superoxide anion (O˙-2 ...
Yuya Fujisawa   +3 more
doaj  

Population structure and genetic diversity of Nile tilapia (Oreochromis niloticus) using microsatellite markers from selected water bodies in southwest Ethiopia

open access: yesVeterinary Medicine and Science, 2023
Background The Ethiopian southwest drainage has been designated a huge potential for fishery and aquaculture development. However, the genetic diversity of Nile tilapia along the main water bodies has yet to be uncovered.
Seid Mohammed Ahmed   +3 more
doaj   +1 more source

Molecular Genetics of Turcot’s Syndrome

open access: yesPediatric Neurology Briefs, 1995
Genetic abnormalities in 13 of 14 families with concurrent primary brain tumors and multiple colorectal adenomas (Turcot’s syndrome) are reported from the Johns Hopkins University School of Medicine and other centers.
J Gordon Millichap
doaj   +1 more source

Understanding the Molecular Genetics of Basal Cell Carcinoma

open access: yesInternational Journal of Molecular Sciences, 2017
Basal cell carcinoma (BCC) is the most common human cancer and represents a growing public health care problem. Several tumor suppressor genes and proto-oncogenes have been implicated in BCC pathogenesis, including the key components of the Hedgehog ...
C. Pellegrini   +5 more
semanticscholar   +1 more source

Molecular genetics of cataract.

open access: yesIndian Journal of Ophthalmology, 2000
Studies on hereditary congenital cataracts have led to the identification of genes involved in formation of these cataracts. Knowledge of the structure and function of a particular gene and the effect of disease-associated mutations on its function are ...
Kannabiran Chitra, Balasubramanian D.
doaj  

Molecular Genetics of Stroke

open access: yesSiriraj Medical Journal, 2008
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Manop Pithukpakorn
doaj  

The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis.

open access: yesArthritis & Rheumatism, 1987
Aucun gene HLA seul n'a ete identifie comme conferant un risque de maladie. Distinction et definition des sous-types DR4. Role de la 3eme region hypervariable de DRβ1.
P. Gregersen, J. Silver, R. Winchester
semanticscholar   +1 more source

Molecular Genetics of Mycobacteriophages

open access: yesMicrobiology Spectrum, 2014
ABSTRACTMycobacteriophages have provided numerous essential tools for mycobacterial genetics, including delivery systems for transposons, reporter genes, and allelic exchange substrates, and components for plasmid vectors and mutagenesis. Their genetically diverse genomes also reveal insights into the broader nature of the phage population and the ...
openaire   +4 more sources

The molecular genetics of the telomere biology disorders

open access: yesRNA Biology, 2016
The importance of telomere function for human health is exemplified by a collection of Mendelian disorders referred to as the telomere biology disorders (TBDs), telomeropathies, or syndromes of telomere shortening. Collectively, the TBDs cover a spectrum
A. Bertuch
semanticscholar   +1 more source

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