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Non-adiabatic effects in F + CHD3 reactive scattering
(American Institute of Physics, 2017-06)
The effect of non-adiabatic transitions on the F(2P) + CHD3(ν1) → DF + CHD2 and F(2P) + CHD3(ν1) → HF + CD3 reactions is investigated. The dynamics of the nuclei was simulated using trajectory surface hopping and a ...
Communication: Mode specific quantum dynamics of the F + CHD3 → HF + CD3 reaction
(American Institute of Physics, 2016-05)
The mode specific reactivity of the F + CHD3 → HF + CD3 reaction is investigated using an eight-dimensional quantum dynamical model on a recently developed ab initio based full-dimensional potential energy surface. Our ...
Cloning and characterization of a novel alternatively spliced transcript of the human CHD7 putative helicase
(2010)
Abstract
Background
The CHD7 (Chromodomain Helicase DNA binding protein 7) gene encodes a member of the chromodomain family of ATP-dependent chromatin remodeling enzymes. Mutations in the CHD7 gene are found in ...
A cheap and quick method for DNA-based sexing of birds
(Waterbird Society, 2008-09)
Although the collection of air-dried blood samples on filter paper has been used for field work as a routine, it has required the use of special and expensive types of paper. In the present manuscript the use of common ...
Deletion of the RMGA and CHD2 genes in a child with epilepsy and mental deficiency
(ELSEVIER SCIENCE BVAMSTERDAM, 2012)
We describe a novel chromosome microdeletion at 15q26.1 detected by oligo-array-CGH in a 6-year-old girl presenting with global development delay, epilepsy, autistic behavior and facial dysmorphisms. Although these features ...
Characterization of new FIR laser lines from CHD2OH
(Ieee-inst Electrical Electronics Engineers IncPiscatawayEUA, 2005)
Sex determination in Turdus amaurochalinus (Passeriformes: Muscicapidae): morphometrical analysis supported by CHD gene
(Universidad de Costa Rica, 2011)
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency
(National Academy of Sciences, 2014)
© 2014, National Academy of Sciences. All rights reserved. Inactivating mutations in chromodomain helicase DNA binding protein 7 (CHD7) cause CHARGE syndrome, a severe multiorgan system disorder of which Isolated ...
The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression
(Amer Soc Clinical Investigation Inc, 2017-03-01)
The mechanisms underlying the neurodevelopmental deficits associated with CHARGE syndrome, which include cerebellar hypoplasia, developmental delay, coordination problems, and autistic features, have not been identified. ...