scholarly journals Identification and characterization of candidate genes influencing salinity tolerance in Macrobrachium australiense : a model for the molecular basis of colonization of low ionic environments

Author(s):  
Azam Moshtaghi
2004 ◽  
Vol 14 (1) ◽  
pp. 59-69 ◽  
Author(s):  
Tushar R. Bhangale ◽  
Mark J. Rieder ◽  
Robert J. Livingston ◽  
Deborah A. Nickerson

2001 ◽  
Vol 110 (2) ◽  
pp. 111-121 ◽  
Author(s):  
Ester Rozenblum ◽  
Pia Vahteristo ◽  
Therese Sandberg ◽  
Jon Bergthorsson ◽  
Kirsi Syrjakoski ◽  
...  

2005 ◽  
Vol 57 (9) ◽  
pp. 636-643 ◽  
Author(s):  
Jae-Jung Kim ◽  
Hyun-Hee Kim ◽  
Joo-Hyun Park ◽  
Ha-Jung Ryu ◽  
JuYoung Kim ◽  
...  

2007 ◽  
Vol 15 (4) ◽  
pp. 422-431 ◽  
Author(s):  
Dries Castermans ◽  
Joris R Vermeesch ◽  
Jean-Pierre Fryns ◽  
Jean G Steyaert ◽  
Wim J M Van de Ven ◽  
...  

1998 ◽  
Vol 275 (3) ◽  
pp. F319-F324 ◽  
Author(s):  
Hiroyasu Tsukaguchi ◽  
Chairat Shayakul ◽  
Urs V. Berger ◽  
Matthias A. Hediger

Facilitated urea transporters (UTs) are responsible for urea accumulation in the renal inner medulla of the mammalian kidney and therefore play a central role in the urinary concentrating process. Recently, the cDNAs encoding three members of the UT family, UT1, UT2, and UT3 have been cloned. These transporters are expressed in different structures of the mammalian kidney. In rat, UT1 resides in the apical membrane of terminal inner medullary collecting ducts, where it mediates vasopressin-regulated urea reabsorption. UT2 and UT3 are located in descending thin limbs of Henle’s loop and descending vasa recta, respectively, and participate in urinary recycling processes, which minimize urea escape from the inner medulla. UT1 and UT2 are regulated independently and respond differently to changes in dietary protein content and hydration state. Identification and characterization of these urea transporters advances our understanding of the molecular basis and regulation of the urinary concentrating mechanism.


2000 ◽  
Vol 44 (2) ◽  
pp. 437-440 ◽  
Author(s):  
Jun Ishikawa ◽  
Atsuko Sunada ◽  
Ritsuko Oyama ◽  
Kunimoto Hotta

ABSTRACT We determined the molecular basis for the enhanced expression of the aac(3)-Xa gene encoding an aminoglycoside 3-N-acetyltransferase in Streptomyces griseus. A C→T substitution was identified at the putative promoter of the mutant gene. RNA analyses demonstrated that the substitution caused a marked increase in the production of the gene-specific transcripts. Therefore, it seemed very likely that the aac(3)-Xa gene was activated by the substitution resulting in the emergence of a stronger promoter.


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