Keywords: AGC2; aspartate-glutamate carrier-2; CTLN-2; adult-onset type II citrullinemia; FFA; free fatty acid; MA shuttle; malate-aspartate shuttle; MC shuttle; malate-citrate shuttle; TCA; tricarboxylic acid; Citrin deficiency; Adult-onset type II citrullin
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: 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
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
Keywords: Inborn errors of metabolism; Wilson disease; Alpha-1 antitrypsin deficiency; Citrin deficiency; HFE-associated hemochromatosis;
Molecular and clinical characterization of citrin deficiency in a cohort of Chinese patients in Hong Kong
Keywords: Citrin deficiency; NICCD; FTTDCD; CTLN2; Hemangioendothelioma;
SLC25A13 c.1610_1612delinsAT mutation in an Indian patient and literature review of 79 cases of citrin deficiency for genotype-phenotype associations
Keywords: CD; citrin deficiency; NICCD; neonatal intrahepatic cholestasis; CTLN2; citrullinemia type 2; FTTDCD; failure to thrive and dyslipidemia; SLC25A13; solute carrier family 25 member 13; INH; idiopathic neonatal hepatitis; ALP; alkaline phosphatase; ALT; ala
A 73-year-old patient with adult-onset type II citrullinemia successfully treated by sodium pyruvate and arginine
Keywords: Citrin deficiency; CTLN2; Aged patients; Hepatic encephalopathy; Sodium pyruvate;
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
Citrin deficiency and current treatment concepts
Keywords: Adult-onset type II citrullinemia (CTLN2); Carbohydrate toxicity; Citrin deficiency; Hyperammonemia; Mitochondrial aspartate–glutamate carrier; Neonatal intrahepatic cholestasis (NICCD); SLC25A13; Sodium pyruvate
An autopsy case with adult onset type II citrullinemia showing myelopathy
Keywords: Citrullinemia; Urea cycle disorders; Citrin deficiency; Hepatic encephalopathy; Hepatic myelopathy
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
Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice
Keywords: Adult-onset type II citrullinemia; Hyperammonemia; Argininosuccinate synthetase; Citrin deficiency; Pyruvate; Redox state; UreogenesisAGC, aspartate-glutamate carrier; Ala, alanine; Arg, arginine; Asn, asparagine; Asp, aspartate; ASS, argininosuccinate sy