Results 161 to 170 of about 76,819 (327)

Taurolithocholate-Induced Cholestasis: Taurocholate, but not Dehydrocholate, Reverses Cholestasis and Bile Canalicular Membrane Injury

, 1977
Thomas J. Layden, James L. Boyer
openalex   +1 more source

Cholestasis in amoebic liver abscess. [PDF]

, 1985
Pranesh Nigam, Anju Gupta, Komal Kapoor, Guru Sharan, Binita Goyal, L D Joshi   +5 more
openalex   +1 more source

Farnesoid X Receptor Regulation of the NLRP3 Inflammasome Underlies Cholestasis-Associated Sepsis.

Cell Metabolism, 2017
H. Hao, L. Cao, Changtao Jiang, Y. Che, Songyang Zhang, Shogo Takahashi, Guangji Wang, F. Gonzalez   +7 more
semanticscholar   +1 more source

Anti‐Ro52/TRIM21 autoantibodies predict Sjögren's syndrome in patients with primary biliary cholangitis

Hepatology Research, EarlyView.
Abstract Background and aims Sjögren's syndrome is a common comorbidity in patients with primary biliary cholangitis (PBC). Anti‐Ro52 autoantibodies against the protein TRIM21 are often seen in Sjögren's syndrome. TRIM21 consists of four domains (PRY/SPRY, Coiled‐Coil, B‐box, and RING domain), each with a specific function.
Marie Louise Næstholt Dahl, Trine‐Line Korsholm, Jakob Hauge Mikkelsen, Malene Hvid, Ayad Babaee, Matias Hauge Böttcher, Jesper Bach Hansen, Peter Holland‐Fischer, Christian Brix Folsted Andersen, Henning Grønbæk, Bent Deleuran   +10 more
wiley   +1 more source

Alterations in the gut microbiota in individuals with infantile cholestasis: a comparison of high- and low-γ-glutamyltransferase subtypes. [PDF]

Transl Pediatr
Lin Y, Ye H, Chen Y, Ou W, Zhang R.
europepmc   +1 more source

Reversal of Intrahepatic Cholestasis of Pregnancy in Women after High Dose S-Adenosyl-L-Methionine Administration† [PDF]

, 1984
M Frezza, Gabriele Pozzato, L. Chiesa, Giorgio Stramentinoli, C. Di Padova   +4 more
openalex   +1 more source

Lipolysis‐Stimulated Lipoprotein Receptor Gene Variants as a Cause of Progressive Familial Intrahepatic Cholestasis: A Case Report

Hepatology Research, EarlyView.
This article talks about a rare genetic condition called LSR deficiency, which causes liver issues such as another condition called PFIC. It describes the case of a 4‐year‐old girl who had yellowing of the skin, slow growth, and liver problems and was diagnosed with LSR deficiency through genetic testing. The study suggests that LSR could be a new type
Yugo Takaki, Shuichiro Umetsu, Yoshihiko Sugino, Takahiro Yamashita, Takehiko Doi, Kazuo Imagawa, Shogo Ito, Yutaro Mihara, Hisamitsu Hayashi, Ayano Inui   +9 more
wiley   +1 more source

Genetic Variants and Long-Term Outcomes in Korean Children with Progressive Familial Intrahepatic Cholestasis. [PDF]

Pediatr Gastroenterol Hepatol Nutr
Choi S, Kim Y, Park S, Ahn JE, Kim L, Shin M, Lee KJ, Moon JS, Ko JS.   +8 more
europepmc   +1 more source

Cholestasis Associated With Extrabiliary Hodgkin’s Disease

, 1974
David Perera, Martin L. Greene, Laura Fenster   +2 more
openalex   +1 more source

Systematic review of progressive familial intrahepatic cholestasis.

Clinics And Research in Hepatology and Gastroenterology, 2019
A. Baker, N. Kerkar, L. Todorova, B. Kamath, R. Houwen   +4 more
semanticscholar   +1 more source