Premature senescence caused by potassium deficiency has been most severe on soils that 0 are considered deficient or marginal in potassium for cotton growth ie. having a soil testresult less than
This implied that a combination of salt stress and K + deficiency impaired the light reaction pathways of PSI and II in maize seedlings. 展开 关键词: Combined stresses Salt stress Potassium-deficiency Maize Chlorophyll fluorescence DOI: 10.1016/j.envexpbot.2011.08.019 被引量: 69 ...
www.nature.com/scientificreports OPEN Cognitive deficits caused by a disease-mutation in the α3 Na+/K+-ATPase isoform received: 02 June 2016 accepted: 01 August 2016 Published: 23 August 2016 Thomas Hellesøe Holm1,2, Toke Jost Isaksen1,2, Simon Glerup1, Anders Heuck1,2...
One of the most interesting causes of nontraumatic rhabdomyolysis is potassium deficiency caused by a variety of reasons. Familial hypokalemic periodic paralysis is a rare genetic disease characterized by periodic attacks of muscle weakness due to decreases in serum potassium without other detectable ...
These brown tips are also the result of a nutrient deficiency. Not only is the pH too high, but the thick soil also made it harder for plant roots to get access to nutrients.This looks like a potassium deficiency, which is often caused by too-high pH...
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency We report the first four cases of infantile mitochondrial encephalopathies caused by mutations in the ND3 subunit gene. Three unrelated children have the ... R Mcfarland,DM...
In contrast, glucose tolerance was unaffected by ovariectomy in age-matched female MafAS64F/+ mice (data not shown; Figure S5A). These results indicate that the effects of the MafAS64F variant is dominant over the effects of estrogen deficiency on glucose intolerance. Furthermore, testosterone...
Linkage studies and mutation analysis were performed in two Swedish families with hyperkalemic periodic paralysis (HYPP), an autosomal dominant inherited disorder characterized by episodic muscle weakness associated with increasing or high levels of serum potassium. The gene for HYPP is the gene encoding...
44, No. 12, 707-722, December 2012 Human skeletal dysplasia caused by a constitutive activated transient receptor potential vanilloid 4 (TRPV4) cation channel mutation Sang Sun Kang1,4, Sung Hwa Shin1, Chung-Kyoon Auh3 and Jaesun Chun2 1Department of Biology Education Chungbuk National ...
Disrupting this balance is sufficient to induce a progressive age-dependent ataxia with neurodegeneration. It is proposed that damage to the spectrin based MPS by excessive calpain activity may be a consequential event contributing to the pathology of many ataxias and neurodegenerative disorders....