Insight into bile duct differentiation takes (notched) wings

Biallelic TXNIP deficiency is associated with a multisystemic metabolic disease.

Molecular metabolism·2026

Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.

PloS one·2025

Extrahepatic biliary atresia and normal-range serum gamma-glutamyltranspeptidase activity: A case report.

JPGN reports·2024

Langerhans Cell Histiocytosis or Acute Cellular Rejection?

Pediatric transplantation·2024

Steatotic liver disease associated with 2,4-dienoyl-CoA reductase 1 deficiency.

International journal of obesity (2005)·2024

Kinesin family member 12-related hepatopathy: A generally indolent disorder with elevated gamma-glutamyl-transferase activity.

Clinical genetics·2024

With no lysine kinase 1 in hepatic stellate cells promotes mouse and human liver fibrosis through glycolytic triosephosphate isomerase 1.

Hepatology (Baltimore, Md.)·2026

Nucleos(t)ide withdrawal vs Nucleos(t)ide withdrawal with adjuvant pegylated-interferon in HBeAg-negative hepatitis B virus infection (NUC-B Trial).

Hepatology (Baltimore, Md.)·2026

Hepatocyte MLKL drives obesity-driven hepatocellular carcinoma progression via mitochondrial dysfunction independent of necroptosis in MASLD.

Hepatology (Baltimore, Md.)·2026

Weight reduction-dependent/-independent effects of survodutide on liver endpoints: Mediation analysis of a phase 2 trial in MASH.

Hepatology (Baltimore, Md.)·2026

Implications of new obesity definitions in the classification and outcomes of patients with MASLD.

Hepatology (Baltimore, Md.)·2026

Recompensation of decompensated cirrhosis in a spectrum of metabolic dysfunction-related steatotic liver disease, with PEth-corroborated alcohol abstinence and modification of cardiometabolic risk factors.

Hepatology (Baltimore, Md.)·2026

Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.

Acta crystallographica. Section F, Structural biology communications·2026

Recurrent episodes of hypoglycemia as an initial presentation of pituitary stalk interruption syndrome: A case report.

Radiology case reports·2026

Dopamine Receptor D2 gene Polymorphisms rs2005313, rs4274224, and rs4938019 in Pakistani Patients with Schizophrenia:a Diagnostic Tool for Schizophrenia.

Journal of molecular neuroscience : MN·2026

Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.

Clinical endocrinology·2026

CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.

European journal of endocrinology·2026

Integrating Brain Morphological Features and Ionized Serum Magnesium to Identify Mild Tic Comorbidity in Children with Autism Spectrum Disorder.

Neuropsychiatric disease and treatment·2026

Related Experiment Videos

Insight into bile duct differentiation takes (notched) wings

Related Concept Videos

Biallelic TXNIP deficiency is associated with a multisystemic metabolic disease.

Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.

Extrahepatic biliary atresia and normal-range serum gamma-glutamyltranspeptidase activity: A case report.

Langerhans Cell Histiocytosis or Acute Cellular Rejection?

Steatotic liver disease associated with 2,4-dienoyl-CoA reductase 1 deficiency.

Kinesin family member 12-related hepatopathy: A generally indolent disorder with elevated gamma-glutamyl-transferase activity.

With no lysine kinase 1 in hepatic stellate cells promotes mouse and human liver fibrosis through glycolytic triosephosphate isomerase 1.

Nucleos(t)ide withdrawal vs Nucleos(t)ide withdrawal with adjuvant pegylated-interferon in HBeAg-negative hepatitis B virus infection (NUC-B Trial).

Hepatocyte MLKL drives obesity-driven hepatocellular carcinoma progression via mitochondrial dysfunction independent of necroptosis in MASLD.

Weight reduction-dependent/-independent effects of survodutide on liver endpoints: Mediation analysis of a phase 2 trial in MASH.

Implications of new obesity definitions in the classification and outcomes of patients with MASLD.

Recompensation of decompensated cirrhosis in a spectrum of metabolic dysfunction-related steatotic liver disease, with PEth-corroborated alcohol abstinence and modification of cardiometabolic risk factors.

Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.

Recurrent episodes of hypoglycemia as an initial presentation of pituitary stalk interruption syndrome: A case report.

Dopamine Receptor D2 gene Polymorphisms rs2005313, rs4274224, and rs4938019 in Pakistani Patients with Schizophrenia:a Diagnostic Tool for Schizophrenia.

Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.

CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.

Integrating Brain Morphological Features and Ionized Serum Magnesium to Identify Mild Tic Comorbidity in Children with Autism Spectrum Disorder.

Related Experiment Videos

Insight into bile duct differentiation takes (notched) wings

Related Concept Videos

Related Articles