Keywords: AGC; aspartate-glutamate carrier; AN; adenine nucleotide; ANOVA; analysis of variance; Asp; aspartate; bw; body weight; cGPD; cytosolic glycerol-3-phosphate dehydrogenase; CTLN2; adult-onset type II citrullinemia; Ctrn-KO; citrin (a.k.a., Slc25a13) knocko
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: ALGS; Alagille syndrome; ALT; Alanine aminotransferase; AR; Autosomal-recessive inheritance; AST; Aspartate aminotransferase; BRIC; Benign recurrent intrahepatic cholestasis; CNV; Copy number variation; D.Bil; Direct bilirubin; DJS; Dubin-Johnson syndrome
Keywords: αKG; α-ketoglutarate; AGC; aspartate-glutamate carrier; Ala; alanine; AOA; aminooxyacetate; Arg; arginine; ASA; argininosuccinate; Asp; aspartate; Cit; citrulline; CTLN2; adult-onset type II citrullinemia; Cr; creatinine; DHAP; dihydroxyacetone phosphat
Bile acid profiles in neonatal intrahepatic cholestasis caused by citrin deficiency
Keywords: NICCD; neonatal intrahepatic cholestasis caused by citrin deficiency; CYP7A1; cholesterol 7α-hydroxylase; CA; cholic acid; CDCA; chenodeoxycholic acid; DCA; deoxycholic acid; LCA; lithocholic acid; ROC; receiver operating characteristic; AGC; aspartate-g
Molecular analysis of SLC25A13 gene in human peripheral blood lymphocytes: Marked transcript diversity, and the feasibility of cDNA cloning as a diagnostic tool for citrin deficiency
Keywords: CD; citrin deficiency; cDNA; complementary Deoxyribonucleic acid; ORF; open reading frame; RT-PCR; reverse transcription-polymerase chain reaction; NICCD; neonatal intrahepatic cholestasis caused by citrin deficiency; LSM; lymphocyte separation medium; ED
Diagnosis of Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency Using High-Resolution Melting Analysis and a Clinical Scoring System
Keywords: ALT; Alanine aminotransferase; CTLN2; Adult-onset type 2 citrullinemia; HRM; High-resolution melting; NICCD; Neonatal intrahepatic cholestasis caused by citrin deficiency; PCR; Polymerase chain reaction; SNP; Single-nucleotide polymorphism;
Effects of supplementation on food intake, body weight and hepatic metabolites in the citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mouse model of human citrin deficiency
Keywords: AGC; aspartate-glutamate carrier; ASS; argininosuccinate synthetase; CTLN2; adult-onset type II citrullinemia; Ctrn-KO; Slc25a13 (citrin) knockout; KO; knockout; MCT; medium-chain triglycerides; mGPD; mitochondrial glycerol-3-phosphate dehydrogenase; NI
Metabolomic analysis reveals hepatic metabolite perturbations in citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mice, a model of human citrin deficiency
Keywords: AASS; α-aminoadipate δ-semialdehyde synthase; AGC; aspartate-glutamate carrier; αKG; α-ketoglutarate; ANOVA; analysis of variance; Ala; alanine; Arg; arginine; ASA; argininosuccinate; Asp; aspartate; ASS; argininosuccinate synthetase; CE/MS; capilla
Sustaining hypercitrullinemia, hypercholesterolemia and augmented oxidative stress in Japanese children with aspartate/glutamate carrier isoform 2-citrin-deficiency even during the silent period
Keywords: Aspartate/glutamate carrier isoform 2-citrin; Neonatal intrahepatic cholestasis caused by citrin deficiency; Adult-onset type II citrullinemia; Silent period; Amino acids; Carbohydrates; Hypercholesterolemia; Oxidative stress
Citrin deficiency as a cause of chronic liver disorder mimicking non-alcoholic fatty liver disease
Keywords: AGC; aspartate-glutamate carrier; NADH; nicotinamide adenine dinucleotide; ATP; adenosine triphosphate; ASS; argininosuccinate synthetase; NICCD; neonatal intrahepatic cholestasis caused by citrin deficiency; CTLN2; adult-onset type II citrullinemia; NA
Novel diagnostic approach to citrin deficiency: Analysis of citrin protein in lymphocytes
Keywords: Citrin deficiency; Neonatal intrahepatic cholestasis caused by citrin deficiency; Adult-onset type II citrullinemia; SLC25A13 gene
A possible mechanism of neonatal intrahepatic cholestasis caused by citrin deficiency
Keywords: Neonatal cholestasis; Citirn deficiency; AGC; aspartate/glutamate carrier; ASS; argininosuccinate synthetase deficiency; BC; biliary cirrhosis; CA; cholic acid; CDC; chenodeoxycholic acid; CTLN2; adult-onset citrullinemia type II; EBA; extrahepatic biliar