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「"Alpini G"[Author]」の検索結果

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The Functional Role of the Secretin/Secretin Receptor Signaling During Cholestatic Liver Injury.

Knockout of the tachykinin receptor 1 in the Mdr2 mouse model of primary sclerosing cholangitis reduces biliary damage and liver fibrosis.

The Tumor Microenvironment in Cholangiocarcinoma Progression.

Downregulation of p16 decreases biliary damage and liver fibrosis in the Mdr2-/- mouse model of primary sclerosing cholangitis.

Pro-inflammatory signalling and gut-liver axis in non-alcoholic and alcoholic steatohepatitis: Differences and similarities along the path.

Concise Review: Functional Roles and Therapeutic Potentials of Long Non-coding RNAs in Cholangiopathies.

Hepatocyte Autophagy: Maintaining a Toxic-Free Environment.

H2 histamine receptor Vivo-Morpholino treatment ameliorates large bile duct damage in mice deficient in ATP binding cassette subfamily B member 4 (Abcb4-/-) via down-regulation of cAMP/ERK signaling.

Cholangiocarcinoma: novel therapeutic targets.

Neuroendocrine Changes in Cholangiocarcinoma Growth.

Bile Acid Receptor Therapeutics Effects on Chronic Liver Diseases.

Melatonin and circadian rhythms in liver diseases: Functional roles and potential therapies.

Biliary damage and liver fibrosis are ameliorated in a novel mouse model lacking l-histidine decarboxylase/histamine signaling.

Indole Alleviates Diet-induced Hepatic Steatosis and Inflammation in a Manner Involving Myeloid Cell PFKFB3.

Correction to: Knockout of α-calcitonin gene-related peptide attenuates cholestatic liver injury by differentially regulating cellular senescence of hepatic stellate cells and cholangiocytes.

The emerging role of cellular senescence in renal diseases.

Maternal diet intervention before pregnancy primes offspring lipid metabolism in liver.

Role of Non-Coding RNAs in the Progression of Liver Cancer: Evidence from Experimental Models.

The challenges of primary biliary cholangitis: What is new and what needs to be done.

Knockdown of vimentin reduces mesenchymal phenotype of cholangiocytes in the Mdr2 mouse model of primary sclerosing cholangitis (PSC).

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