نتایج جستجو برای: mutant strains

تعداد نتایج: 270616  

The structural requirements for the inhibitor activity of various furan carboxanilide derivatives against succinate dehydrogenase complex (SDC) activity in mitochondria of either wild or mutant strains of Ustilago maydis were investigated with the aid of Hansch QSAR analysis. It has been found that the inhibitor activity against both types of enzymes is best related to the ??? or ??M of th...

Journal: :iranian journal of veterinary medicine 2014
saeed salari taghi zahraei salehi bahar nayeri fasaei vahid karimi

background: colibacillosis, caused by different serotypes of avian pathogenic escherichia coli (apec), is one of the important diseases in poultry industry. the isolate o78 is the most prevalent serotype of apec in iran. one of the apec virulence factors, increased serum survival (iss) gene, is related to serum resistance. the usual form of colibacillosis in avian is extraintestinal, and serum ...

Journal: :محیط شناسی 0
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this study was conducted to determine physiological and morphological variation of strains of the ectomycorrhizal fungus hebeloma cylindrosporum associated with pinus pinaster and its consequence on the symbiotic processes in coastal forests adjacent to bordeaux, south west france, from 2003-2005. mycelial cultures were conducted in the laboratory on a rich medium (ymg). diploid fungal strains ...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2012
Clare Puddifoot Marc-Andre Martel Francesc X Soriano Alberto Camacho Antonio Vidal-Puig David J A Wyllie Giles E Hardingham

Underexpression of the transcriptional coactivator PGC-1α is causally linked to certain neurodegenerative disorders, including Huntington's Disease (HD). HD pathoprogression is also associated with aberrant NMDAR activity, in particular an imbalance between synaptic versus extrasynaptic (NMDAR(EX)) activity. Here we show that PGC-1α controls NMDAR(EX) activity in neurons and that its suppressio...

Journal: :Genetics and molecular research : GMR 2014
J Q Sheng J H Wang S H He L G Zeng K Peng Y J Hong

Carassius auratus var. pingxiangnensis is a natural triploid crucian carp mutant. In order to understand its placement and genetic background at the gene level, the characteristics of mitochondrial DNA sequences and phylogenetic relationship were examined. The results showed that the mitochondrial DNA is a circular double-stranded DNA molecule that is 16,576 bp in length with 13 protein-coding ...

Journal: :Genetics 1970
J A Metcalfe

HE mutant alleles of the dumpy locus produce a number of phenotypic Teffects, viz., an obliquity of the wings ( 0 ) , a lethal effect (1) , and hypodermal irregularities of the thorax called vortices (v) . The genetics of the dumpy locus has been described by CARLSON (1959). The alleles may express any one of the three effects singly (dp", d p z , dp") or in any combination with one another (dp...

Journal: :Antimicrobial agents and chemotherapy 2005
Kok-Fai Kong Suriya Ravi Jayawardena Shalaka Dayaram Indulkar Aimee Del Puerto Chong-Lek Koh Niels Høiby Kalai Mathee

In members of the family Enterobacteriaceae, ampC, which encodes a beta-lactamase, is regulated by an upstream, divergently transcribed gene, ampR. However, in Pseudomonas aeruginosa, the regulation of ampC is not understood. In this study, we compared the characteristics of a P. aeruginosa ampR mutant, PAOampR, with that of an isogenic ampR+ parent. The ampR mutation greatly altered AmpC produ...

2009
Kian Hoe Khoo Andreas C. Joerger Stefan M.V. Freund Alan R. Fersht

The core domain of the tumour suppressor p53 is of inherently low thermodynamic stability and also low kinetic stability, which leads to rapid irreversible denaturation. Some oncogenic mutations of p53 act by just making the core domain thermosensitive, and so it is the target of novel anti-cancer drugs that bind to and stabilise the protein. Increasing the stability of the unstable core domain...

Journal: :The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry 2011
Amber L Southwell Paul H Patterson

Huntingtin, the protein that when mutated causes Huntington disease (HD), has many known interactors and participates in diverse cellular functions. Mutant Htt (mHtt) engages in a variety of aberrant interactions that lead to pathological gain of toxic functions as well as loss of normal functions. The broad symptomatology of HD, including diminished voluntary motor control, cognitive decline, ...

Journal: :Human molecular genetics 2003
I Jill Karolyi Frank J Probst Lisa Beyer Hana Odeh Gary Dootz Kelly B Cha Donna M Martin Karen B Avraham David Kohrman David F Dolan Yehoash Raphael Sally A Camper

The unconventional myosin genes Myo15, Myo6 and Myo7a are essential for hearing in both humans and mice. Despite the expression of each gene in multiple organs, mutations result in identifiable phenotypes only in auditory or ocular sensory organs. The pirouette (pi) mouse also exhibits deafness and an inner ear pathology resembling that of Myo15 mutant mice and thus may be functionally related ...

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