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Showing 1-28 of 28 results for "11814770001" within Papers
Reza Ranjbar et al.
BMC microbiology, 16, 40-40 (2016-03-15)
Up to now, fecal-oral and oral-oral are the most commonly known routes for transmission of H. pylori, therefore, contaminated water can play an important role in transmission of H. pylori to humans. Genotyping using virulence markers of H. pylori is
Mehdi Bamorovat et al.
Iranian journal of public health, 44(10), 1359-1366 (2015-11-18)
Cutaneous leishmaniasis (CL) caused by Leishmania tropica is endemic in Kerman, southeastern Iran. While dogs have long been implicated as the main domestic reservoirs of L. infantum, etiological agent of zoonotic visceral leishmaniasis (ZVL), they can also carry L. tropica
Ali Zare Dehnavi et al.
Human genomics, 15(1), 45-45 (2021-07-21)
Leukodystrophies are the main subgroup of inherited CNS white matter disorders which cause significant mortality and morbidity in early years of life. Diagnosis is mostly based on clinical context and neuroimaging findings; however, genetic tools, particularly whole-exome sequencing (WES), have
Fatemeh Bitarafan et al.
Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 24, 44-44 (2019-06-05)
Dysfunction of polycystin-1 or polycystin-2, the proteins encoded by polycystic kidney disease 1 (PKD1) and PKD2, respectively, are the cause of autosomal dominant PKD (ADPKD). This genetically heterogeneous monogenic disorder is the most common inherited kidney disease. The disease manifests
Shahrzad Atapoor et al.
Jundishapur journal of microbiology, 7(5), e10013-e10013 (2014-08-26)
There is a possibility for the presence of Helicobacter pylori in vegetables due to their close contact with polluted water, soil and feces. This study was carried out to detect the presence of H. pylori in vegetables and salads in
Fatemeh Bitarafan et al.
Journal of clinical laboratory analysis, 34(12), e23544-e23544 (2020-08-31)
The extremely high genetic heterogeneity of hearing loss due to diverse group of genes encoding proteins required for development, function, and maintenance of the complex auditory system makes the genetic diagnosis of this disease challenging. Up to now, 121 different
Lindsay H Levkoff et al.
Neoplasia (New York, N.Y.), 10(8), 804-816 (2008-08-07)
The thymidine analog bromodeoxyuridine (BrdU) is incorporated into newly synthesized DNA and has been shown to increase the susceptibility of incorporating cells to ionizing radiation. However, in the absence of secondary stressors, BrdU is thought to substitute relatively benignly for
Elnaz Saeidi et al.
BioMed research international, 2016, 8701067-8701067 (2016-04-19)
According to controversial theories and results of studies, foods with animal origins play an important role in the transmission of H. pylori to human. The aim of this study was to determine the distribution of vacA genotypes of H. pylori
Miłosz Roliński et al.
Nucleic acids research, 49(3), 1470-1484 (2021-01-15)
Alkylating drugs are among the most often used chemotherapeutics. While cancer cells frequently develop resistance to alkylation treatments, detailed understanding of mechanisms that lead to the resistance is limited. Here, by using genome-wide CRISPR-Cas9 based screen, we identify transcriptional Mediator
Mehdi Bamorovat et al.
Iranian journal of parasitology, 9(3), 342-349 (2015-02-14)
Canine visceral leishmaniasis (CVL) is a systemic disease with a high mortality rate, caused by a diphasic protozoan parasite, Leishmania infantum/chagasi in the world. The objective of the present study was to determine the presence of CVL in the city
VacA, cagA, iceA and oipA genotypes status and antimicrobial resistance properties of Helicobacter pylori isolated from various types of ready to eat foods
Hemmatinezhad B, et al.
Annals of Clinical Microbiology and Antimicrobials, 15(1), 2-2 (2016)
Mehrnoosh Khodaeian et al.
Molecular syndromology, 12(2), 118-126 (2021-05-21)
Kabuki syndrome (KS) is a rare genetic disorder characterized by the following 5 crucial symptoms: dysmorphic facial features, growth retardation, skeletal abnormalities, intellectual disability, and dermatoglyphic malformations. Studies show that most of the KS cases are caused by mutations or
Herbert Tomaso et al.
BMC infectious diseases, 10, 100-100 (2010-04-21)
The detection of Brucellae in tissue specimens using PCR assays is difficult because the amount of bacteria is usually low. Therefore, optimised DNA extraction methods are critical. The aim of this study was to assess the performance of commercial kits
Milad Eidi et al.
BMC neurology, 19(1), 153-153 (2019-07-08)
Multiple Mitochondrial Dysfunctions Syndrome 4 (MMDS4) is manifested as a result of ISCA2 mutations. ISCA2 is a vital component of 4Fe-4S clusters assembly machine. Therefore, in MMDS4 patients, deficient mitochondrial respiratory chain complexes I and II, Aconitase and Succinate dehydrogenase
Jocelyn H Wright et al.
Nucleic acids research, 39(11), e73-e73 (2011-04-05)
Herein, a detailed protocol for a random mutation capture (RMC) assay to measure nuclear point mutation frequency in mouse tissue is described. This protocol is a simplified version of the original method developed for human tissue that is easier to
Fatemeh Bitarafan et al.
Molecular and cellular pediatrics, 8(1), 6-6 (2021-05-11)
Ca2+ as a universal second messenger regulates basic biological functions including cell cycle, cell proliferation, cell differentiation, and cell death. Lack of the protein mitochondrial calcium uptake1 (MICU1), which has been regarded as a gatekeeper of Ca ions, leads to
Ehsan Razmara et al.
Iranian journal of basic medical sciences, 21(3), 333-341 (2018-03-08)
Targeted next-generation sequencing (NGS) provides a consequential opportunity to elucidate genetic factors in known diseases, particularly in profoundly heterogeneous disorders such as non-syndromic hearing loss (NSHL). Hearing impairments could be classified into syndromic and non-syndromic types. This study intended to
Farzane Vafaeie et al.
Cureus, 13(7), e16340-e16340 (2021-08-17)
Fragile X syndrome (FXS) has been reported as the leading cause of mental retardation (MR) that predominantly involves males compared to females. An over-expansion of CGG repeats in the 5' untranslated region of the FMR1 gene plays the primary role
Chunmei Yang et al.
The American journal of pathology, 190(3), 674-688 (2020-01-24)
miRNAs, a well-known group of noncoding RNAs, contribute to the pathogenesis of multiple diseases, including colitis-associated cancer (CAC). Our recent findings indicate that proinflammatory cytokines up-regulate c-MYC level, which subsequently activates cullin 4A and 4B (CUL4A/4B) and CRL4DCAF4 E3 ligases
Reza Ranjbar et al.
FEBS open bio, 6(5), 433-441 (2016-07-16)
Despite the clinical importance of Helicobacter pylori in human gastric disorders, its exact route of transmission is still uncertain. Based on the contentious hypothesis and findings of previous investigations, water may play an important role in the transmission of H.
Soolmaz Mousavi et al.
The journal of venomous animals and toxins including tropical diseases, 20, 51-51 (2014-01-01)
Despite the high importance of Helicobacter pylori, the origin and transmission of this bacterium has not been clearly determined. According to controversial theories and results of previous studies, animal source foods - especially milk - play an important role in
Mehdi Agha Gholizadeh et al.
BMC medical genomics, 15(1), 78-78 (2022-04-06)
Homozygous or compound heterozygous PRUNE1 mutations cause a neurodevelopmental disorder with microcephaly, hypotonia, and variable brain malformations (NMIHBA) (OMIM #617481). The PRUNE1 gene encodes a member of the phosphoesterase (DHH) protein superfamily that is involved in the regulation of cell
Ehsan Razmara et al.
BMC cardiovascular disorders, 18(1), 137-137 (2018-07-05)
Myosin VI, encoded by MYH6, is expressed dominantly in human cardiac atria and plays consequential roles in cardiac muscle contraction and comprising the cardiac muscle thick filament. It has been reported that the mutations in the MYH6 gene associated with
Emad Yahaghi et al.
BioMed research international, 2014, 757941-757941 (2014-09-04)
From a clinical and epidemiological perspective, it is important to know which genotypes and antibiotic resistance patterns are present in H. pylori strains isolated from salads and vegetables. Therefore, the present investigation was carried out to find this purpose. Three
The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families.
Ehsan R, et al.
Iranian Journal of Basic Medical Sciences, 21(3), 333- 341 (2018)
Ehsan Razmara et al.
Molecular genetics & genomic medicine, 8(3), e1118-e1118 (2020-01-17)
Whole-exome sequencing (WES) has emerged as a successful diagnostic tool in molecular genetics laboratories worldwide. In this study, we aimed to find the potential genetic cause of skeletal disease, a heterogeneous disease, revealing the obvious short stature phenotype. In an
Behsan Hemmatinezhad et al.
Annals of clinical microbiology and antimicrobials, 15, 2-2 (2016-01-23)
Despite the high clinical standing of Helicobacter pylori, its exact routes of transmission and origin have not been determined. Based on the contentious hypothesis, foods play an important roles in the transmission of H. pylori to humans. The present study
Fatemeh Bitarafan et al.
Molecular genetics & genomic medicine, 8(8), e1274-e1274 (2020-05-21)
Marfan syndrome (MFS) is a multi-systemic autosomal dominant disease of the connective tissue characterized by the early development of thoracic aneurysms/dissections, along with various manifestations of the ocular and skeletal systems. Due to the genetic and clinical heterogeneity, the clinical
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