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5,281 Possible Causes for Blood, CAG, HD, Molecular, Tissue, [Presence], by, gene, genetics, IN, method, or, repeats

Did you mean: Blood, CAG, HD, Molecular, tics, [Presence], by, gene, genetics, IN, method, or, repeats

  • Acute Kidney Injury

    The laboratory staff were vigilant about this potential interfering substance so repeated the analysis of the creatinine using an enzymatic method that showed a markedly lower[] Methods to measure creatinine clearance in AKI have the potential to improve care for patients with this condition.[] An interplay of the methylation-demethylation machinery controls the process of gene expression.[] We undertook a meta-analysis to evaluate the efficacy of atorvastatin on contrast-induced nephropathy (CIN) after CAG or PCI.[] This review highlights recent advances in the molecular mechanisms of HO-1-mediated cytoprotection and discusses the translational potential of HO-1 induction in AKI.[] BACKGROUND As end-stage liver disease progresses, renal blood flow linearly correlates with mean arterial blood pressure (MBP) due to impaired autoregulation.[] Therefore, inhibiting these processes can significantly protect renal parenchyma from tissue damage.[] Adenine phosphoribosyltransferase (APRT) deficiency is an uncommon genetic cause of chronic kidney disease due to crystalline nephropathy.[] Data was collected on patients who received HD for AKI from September 2014 to December 2016.[] Factors associated with increased inpatients mortality were presence of stage III AKI (OR: 3.20, P 0.04, 95% CI: 1.05-9.72), presence of oliguria (OR: 3.42, P 0.006, 95% CI[]

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  • Bicarbonate

    The aim of this study was to investigate the effect of 3-day serial sodium bicarbonate ingestion on repeated sprint and jump performance.[] This amount of variability could be explained by the error in the methods.[] The human gene for NBCe1 (SLC4A4) produces two major transcripts by alternative promoter usage (kNBCe1, originally cloned from kidney and pNBCe1, pancreatic/general form).[] […] ten patients with renal dysfunction [estimated glomerular filtration rate (eGFR), 60 mL/min/1.73 m(2) or less] who underwent elective or emergency coronary angiography (CAG[] The test uses only the fluid in your blood, not the blood cells or the platelets that help your blood clot .[] […] effect might be dependent on the severity of the decrease in tissue perfusion.[] The cytokinesis-block micronucleus (MN) assay was performed on peripheral blood lymphocytes to evaluate genetic damage.[] In the United States, hemodialysis (HD) is generally performed via a bicarbonate dialysate.[] It is unclear, however, whether this therapy is effective only in the presence of acidosis.[] Variants of the electrogenic sodium bicarbonate cotransporter NBCe2 gene, SLC4A5, are associated with increased blood pressure in several ethnic groups.[]

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  • Huntington's Disease

    The genetic evidence implicates a DNA damage response-related pathway in modulating the pathogenicity of the repeat tracts in HD, and possibly, in other trinucleotide repeat[] Twenty (20) studies met the inclusion criteria, including eighteen (18) that had quantitative outcome measures and two (2) that utilized qualitative methods.[] In the European REGISTRY study 2669 HD expansion gene carriers underwent annual cognitive assessment.[] The transcribed mutant RNA contains expanded CAG repeats that translate into a mutant huntingtin protein.[] The journal Human Molecular Genetics * has now published these research findings (Vol. 15, Nr. 18, 15.[] Image copyright SPL Scientists say they may have found the world's first blood test that predicts when someone at risk is likely to get Huntington's disease and tracks how[] Here we report a postmortem analysis of an individual with HD 6 months after cell transplantation and demonstrate that cells derived from grafted fetal striatal tissue had[] A recent genome-wide association (GWA) study discovered genetic modifiers of Huntington's disease (HD) onset in Europeans.[] JHD typically progresses more rapidly than adult onset HD. CLICK HERE FOR MORE INFORMATION An End To HD? In 1993, researchers identified the gene that causes HD.[] There was presence of posterior oral spillage in liquid and nectar, small amount of pharyngeal residues, and no laryngeal penetration or aspiration in the individuals with[]

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  • Methicillin-resistant Staphylococcus Aureus

    Currently, no standards exist for determining the optimal frequency of repeat antimicrobial susceptibility testing (AST) when an organism is recurrently isolated from the[] […] comparative study conducted among sudanese patients during period from May 2012 to July 2014, Staphylococcus aureus strains were isolated and identified by conventional methods[] The frequency of aac(Ia)-2, aph(3)-IIIa, and ant(4')-Ia genes among MRSA strains, were 64%, 42% and 11.8% respectively.[] The aim of the present study is to examine the prevalence, clinical and molecular characteristics, treatment options and outcome of MRSA intracranial abscess over a period[] Blood culture tests on hospital day 11-one day after ceftaroline initiation-were clear of MRSA.[] Radiographic findings showed hepatic abscesses and soft tissue abscesses around the left femur.[] We hypothesized that some genetic shift in MRSA might cause this phenomenon, and therefore we investigated the genetic profiles among MRSA clinical isolates obtained from[] (HD).[] For binary classification, the AUC values of various ML methods ranged from 0.76 to 0.99 for ST5, ST59, and ST239 types.[] Clostridium difficile PCR on the stool was repeated twice and resulted negative both times.[]

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  • Spinal and Bulbar Muscular Atrophy

    After informed consent. molecular genetic evaluation showed the male fetus to carry the SBMA repeat elongation.[] We previously developed a quantitative analysis method for surface electromyography (SEMG), the clustering index (CI) method.[] Thus, mitotic instability of the AR gene in SBMA may not occur at the level of somatic cells.[] Individuals with CAG repeat lengths greater than 62 have not previously been reported.[] Molecular-genetic analysis is a determining step in setting the diagnosis of spinal and bulbar muscular atrophy (SBMA).[] SBMA patients had lower body mass index, blood glucose, and Hemoglobin A1c, but higher blood pressure, homeostasis model assessment of insulin resistance (HOMA-IR, a marker[] PGD is a valid screening tool for patienst affected of CCA and SBMA to prevent transmission of these genetic diseases from parents to children.[] SBMA was the first identified member of a large class of neurodegenerative diseases now known as CAG-related diseases, which includes Huntington's disease (HD), several types[] The presence of elevated glucose, liver pathology or dyslipidaemia is less consistent features.[] Ten patients (from 7 families) with a genetic diagnosis of Kennedy's disease were screened for the presence of tremor using a standardized clinical protocol and followed up[]

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  • Soft Tissue Sarcoma

    Factors associated with survival after repeat PM were assessed with multivariable Cox models among patients who underwent repeat PM.[] Prior to the introduction of CT scans, radiography and angiography were the only methods for tumor localization.[] Our data showed that the expression of the MDR1 gene was significantly higher in malignant tissue than in the normal tissues of patients with STS.[] This report is novel in that to our knowledge, it is the first complete molecular characterization of an EWSR1-POU5F1 fusion in a soft tissue sarcoma.[] During four cycles of induction chemotherapy, peripheral blood stem cells (PBSCs) were harvested.[] Soft tissue sarcoma is rare cancer that affects the soft tissues that support, surround, and connect organs and body structures.[] The optimization is performed using a genetic algorithm.[] We report a case of superficial soft tissue Ewing sarcoma/PNET as a second cancer in a young patient previously treated for Hodgkin's disease (HD).[] The presence of severe pain and tenderness suggested an inflammatory process.[] It was the presence of dystrophic calcification within the lesion that suggested a mineralizing soft tissue sarcoma such as synovial sarcoma.[]

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  • Erythrocytosis

    Repeat serum erythropoietin levels were in normal and high ranges.[] Noninvasive assessment of excessive erythrocytosis as a screening method for chronic mountain sickness at high altitude. High Alt Med Biol 16:162-168, 2015.[] Rarely, erythrocytosis is caused by hereditary gene mutations.[] Through a mutation (CAC CAG), histidine is replaced by glutamine.[] Erythrocytosis molecular etiology was identify in 25 (36%) of the 70 subjects. High-affinity Hb variants were the most common cause, present in 20% of the cases.[] Mean postoperative blood loss within 24 h was 283 212 mL.[] Local tissue hypoxia in renal allograft does not seem to play an important role in the development of PTE.[] Despite recent important discoveries in the molecular pathogenesis of CE, in about 70% of the patients the genetic causes remain to be identified.[] A 53-year-old man with diabetic nephropathy, with no known disease causing hypoxemia started HD in April 2001.[] His P50 value was mildly decreased, thus we suspected the presence of an Hb variant with a high oxygen affinity.[]

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  • Campylobacter Jejuni

    All sugar components of the trisaccharide repeating unit of the polysaccharide were found to be of the furanose ring form.[] Detection of antibiotic resistance in C. jejuni can be performed with both phenotypic and genotypic methods.[] This report describes a culture-negative splenic abscess in an immunocompetent patient caused by Campylobacter jejuni, as determined by 16S rRNA gene sequencing.[] This study explored the molecular epidemiology of Campylobacter jejuni in Israel over a decade (2003-2012) using multilocus sequence typing (MLST) combined with demographic[] Accessory genetic content was more common among fecal than blood strains, whereas blood strains contained a hybrid capsule locus which partially consisted of C. jejuni subsp[] Immunoproliferative small intestinal disease (also known as alpha chain disease) is a form of lymphoma that arises in small intestinal mucosa-associated lymphoid tissue (MALT[] We then administered i.v. ciprofloxacin and replaced the hemodialysis (HD). The patient recovered and was discharged with maintenance HD.[] Campylobacter jejuni was coincubated with Acanthamoeba castellanii Neff trophozoites at different temperatures, in order to evaluate the C. jejuni ability to grow in presence[] […] and 16S rRNA gene of C. jejuni, respectively, in the multiplex PCR assay.[] Rapid molecular strain typing is critical for effective outbreak investigation and implementation of infection control measures.[]

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  • Myotonic Dystrophy

    […] between repeat size and disease phenotypes.[] method and system.[] In this case, MEF2 affects not only the level of activity of genes but also these bits of RNA that fine-tune the proteins associated with the genes.[] Myotonic dystrophy type 1 (DM1) is caused by (CTG CAG)n-repeat expansion within the DMPK gene and thought to be mediated by a toxic RNA gain of function.[] Molecular genetic testing of the Dystrophia Myotonica-Protein Kinase DMPK gene to detect expansion of CTG repeats is confirmatory.[] There have been some reports showing that the presence of specific miRNAs in blood correlates with DM1.[] Moreover, we compared the relative mRNA transcript levels of CNBP gene in leukocytes and in skeletal muscle tissues from controls and DM2 patients.[] Ophthalmologists can diagnose myotonic dystrophy based on clinical and genetic findings, before the manifestation of systemic abnormalities.[] Fourteen patients with DM1 or HD, and 10 caregivers participated in semistructured interviews. Constant comparative analysis was used to identify themes.[] presence of juvenile DM in youngsters presenting with such a thought disorder.[]

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  • High Protein Diet

    Huntington's disease (HD) is a neurodegenerative disorder caused by the huntingtin (HTT) gene with expanded CAG repeats.[] RESEARCH DESIGN AND METHODS A total of 83 men and women with type 2 diabetes (aged 56.1 /- 7.5 years, BMI 35.4 /- 4.6 kg/m(2)) were randomly assigned to an isocaloric, energy-restricted[] […] metabolism, inflammation in blood cells and in adipose tissue to see if there are any diet-induced alterations and to understand the effect of the higher amino acid uptake at the molecular[] […] glucose ( - 0·5 (sd 0·2) mmol/l, P 0·01), fasting insulin ( - 1·7 (sd 0·7) mIU/l, P 0·01), systolic blood pressure ( - 7·6 (sd 1·7) mmHg, P 0·001) and diastolic blood pressure[] […] and elevated the contents of LPS in serum and colonic tissues.[] In this study, we determined whether a high protein diet would be effective in achieving and maintaining weight loss in a genetically obese model, the New Zealand Obese (NZO[] The objective was to assess the significance of the presence or absence of carbohydrates and the proportion of fat in high-protein diets for affecting appetite suppression[] This article describes the design, methods, and baseline characteristics of study participants enrolled in Pro-HEART, a randomized clinical trial to determine the short term[] We examined the effect of a high-protein diet on the maintenance of reduced BP after weight loss in 420 overweight adults from the Diet, Obesity and Genes study.[] Medical Physiology: A Cellular And Molecular Approach . Elsevier/Saunders. p. 771. ISBN 1-4160-2328-3 . Kalantar-Zadeh K, Fouque D (2 November 2017).[]

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