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Academic Journal

Should We Consider UGT1A1 Mutation Analysis in Evaluating the Prolonged Jaundice of Newborn Infants?

Subjects: NEWBORN infants; JAUNDICE; DEMOGRAPHIC characteristics

  • Source: Neonatal Medicine; Feb2024, Vol. 31 Issue 1, p1-8, 8p

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Academic Journal

Rotor Syndrome Presenting as Dubin-Johnson Syndrome.

Subjects: HEPATOLENTICULAR degeneration; SYNDROMES; GENETIC testing

  • Source: Case Reports in Gastroenterology; 2022, Vol. 16 Issue 2, p452-455, 4p

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Academic Journal

Žloutenka kojeného dítěte.

Subjects: BREAST milk; ENTEROHEPATIC circulation; GENETIC mutation

  • Source: Pediatrie pro Praxi; Oct2023, Vol. 24 Issue 5, p313-315, 3p

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Academic Journal

Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia.

Subjects: BILIRUBIN; GALLSTONES; GENETIC polymorphisms

  • Source: International Journal of Laboratory Hematology. May2019 Supplement S1, Vol. 41, p95-101. 7p.

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Academic Journal

A Comprehensive Bioinformatic Analysis of RNA-seq Datasets Reveals a Differential and Variable Expression of Wildtype and Variant UGT1A Transcripts in Human Tissues and Their Deregulation in Cancers.

Subjects: TUMOR genetics; SEQUENCE analysis; GENETIC mutation

  • Source: Cancers; Jan2024, Vol. 16 Issue 2, p353, 23p

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Academic Journal

The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia.

Subjects: GENETICS; GENETIC mutation; ANALYSIS of variance

  • Source: Children; Jul2023, Vol. 10 Issue 7, p1172, 14p

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Academic Journal

Genetic alterations and molecular mechanisms underlying hereditary intrahepatic cholestasis.

Subjects: CHOLESTASIS; SYMPTOMS; GENETIC mutation

  • Source: Frontiers in Pharmacology; 2023, p1-27, 27p

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Academic Journal

Pitfalls in the Diagnosis of β-Thalassemia Intermedia.

Subjects: *BETA-Thalassemia; *ERYTHROCYTES; *NUCLEOTIDE sequencing

  • Source: Hemoglobin. Jul2021, Vol. 45 Issue 4, p265-268. 4p.

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Academic Journal

Isolated Unconjugated Hyperbilirubinemia in Adults: The Gilbert’s Versus Criggler Najar Syndrome Type 2 Conundrum.

Subjects: HYPERBILIRUBINEMIA; GILBERT disease; PHENOBARBITAL

  • Source: Turkish Journal of Internal Medicine; Oct2022, Vol. 4 Issue 4, p200-203, 4p

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Academic Journal

Metabolic Biomarkers Affecting Cell Proliferation and Prognosis in Polycythemia Vera.

Subjects: BIOMARKERS; POLYCYTHEMIA vera; GENETIC mutation

  • Source: Cancers; Oct2022, Vol. 14 Issue 19, p4913, 15p

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  • 1-10 of  67 results for ""Bilirubin metabolism""