ضم تكساس وكالیفورنیا ونیومكسیكو للولایات المتحدة 1845- 1848
نویسندگان
چکیده
منابع مشابه
Genetic Aspects of Scurvy and the European Famine of 1845–1848
The view of scurvy being exclusively a nutritional disorder needs to be updated. Genetic polymorphisms of HFE and haptoglobin (Hp) may explain the geographic variability of mortality caused by the European famine of the mid-19th century. In this period, potatoes had fallen victim to the potato blight and Ireland was more severely hit than continental Europe. Hereditary hemochromatosis is a gene...
متن کاملARQGA 1845.indd
Background Several scoring was developed for evaluation of children with fecal retention using plain radiograph. There are controversies about specificity and sensitivity of these scoring system. Objectives The aim of this study was to evaluate Barr, Blethyn, and Leech score in evaluation of fecal load in plain radiograph. Methods This case control study was conducted on children aged 2-14 year...
متن کاملDdf189 1845..1854
Autosomal dominant polycystic kidney disease (ADPKD) occurs by germline mutation in PKD1 or PKD2. Evidence of homozygous inactivation of either gene in human cyst lining cells as well as in mouse knockout models strongly supports a two-hit mechanism for cyst formation. Discovery of trans-heterozygous mutations in PKD1 and PKD2 in a minority of human renal cysts has led to the proposal that such...
متن کاملC2lc20677c 1841..1848
Biomolecules inside a microfluidic system can be used to solve computational problems, such as theorem proving, which is an important class of logical reasoning problems. In this article, the Boolean variables (literals) were represented using single-stranded DNA molecules, and theorem proving was performed by the hybridization and ligation of these variables into a double-stranded ‘‘solution’’...
متن کاملDdh197 1839..1848
Human SCO1 and SCO2 are paralogous genes that code for metallochaperone proteins with essential, but poorly understood, roles in copper delivery to cytochrome c oxidase (COX). Mutations in these genes produce tissue-specific COX deficiencies associated with distinct clinical phenotypes, although both are ubiquitously expressed. To investigate the molecular function of the SCO proteins, we chara...
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ژورنال
عنوان ژورنال: Ma?allat? Al-Diras?t Al-Tarbaw?yyat? wa Al-Ins?n?yyat?
سال: 2022
ISSN: ['2357-0377', '2090-7885']
DOI: https://doi.org/10.21608/jehs.2022.257158