Kininogen Family Gene

2020 ◽  
Author(s):  
Keyword(s):  

2020 ◽  
Author(s):  
Keyword(s):  


2004 ◽  
Vol 38 (6) ◽  
pp. 865-867
Author(s):  
Z. A. Shangareeva ◽  
T. V. Viktorova ◽  
A. F. Sagidullin


1986 ◽  
Vol 261 (18) ◽  
pp. 8442-8452 ◽  
Author(s):  
C A Lowell ◽  
D A Potter ◽  
R S Stearman ◽  
J F Morrow


2018 ◽  
Vol 17 (6) ◽  
pp. 1021-1025 ◽  
Author(s):  
Azizollah Yousefi ◽  
Mehri Najafi ◽  
Farzaneh Motamed ◽  
Elham Mahmoudi ◽  
Alireza Zare Bidoki ◽  
...  


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Zhixuan Du ◽  
Qitao Su ◽  
Zheng Wu ◽  
Zhou Huang ◽  
Jianzhong Bao ◽  
...  

AbstractMultidrug and toxic compound extrusion (MATE) proteins are involved in many physiological functions of plant growth and development. Although an increasing number of MATE proteins have been identified, the understanding of MATE proteins is still very limited in rice. In this study, 46 MATE proteins were identified from the rice (Oryza sativa) genome by homology searches and domain prediction. The rice MATE family was divided into four subfamilies based on the phylogenetic tree. Tandem repeats and fragment replication contribute to the expansion of the rice MATE gene family. Gene structure and cis-regulatory elements reveal the potential functions of MATE genes. Analysis of gene expression showed that most of MATE genes were constitutively expressed and the expression patterns of genes in different tissues were analyzed using RNA-seq. Furthermore, qRT-PCR-based analysis showed differential expression patterns in response to salt and drought stress. The analysis results of this study provide comprehensive information on the MATE gene family in rice and will aid in understanding the functional divergence of MATE genes.



1998 ◽  
Vol 11 (2) ◽  
pp. 71-77 ◽  
Author(s):  
Stephen Salloway ◽  
Joseph Hong

Mental disorders due to cerebral microvascular disease have been known for over 100 years. Recently, an autosomal dominant form of cerebral arteriopathy (CADASIL) has been described in association with a Notch3 family gene on the short arm of chromosome 19. CADASIL causes subcortical lacunar infarction and dementia in over 80% of cases and depression in a large proportion of patients. Clinically, CADASIL may appear to be very similar to hypertensive microvascular disease (Binswanger's disease), a condition that is seen in the elderly. This article reviews the clinical, pathologic, and genetic features of CADASIL. CADASIL is of interest to neurologists and psychiatrists because it is the first syndrome of vascular dementia and depression with an identified gene. How the gene causes the widespread arteriopathy is not yet known. Insights gained from the study of CADASIL should help us better understand its etiology, as well as the options for treatment of the more common forms of microvascular disease seen in the elderly.



1992 ◽  
Vol 17 ◽  
pp. 123
Author(s):  
Motohide Takemura ◽  
George Uhl
Keyword(s):  


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