Results 101 to 110 of about 4,690 (123)

A Very Rare Setx Gene Variant (C.2750T>C) In a 72-year-old Man with Amyotrophic Lateral Sclerosis and an Unremarkable Family History. Should Genetic Testing be Routinely Performed in all Patients? [PDF]

Eur J Case Rep Intern Med
Posa A, Kornhuber M.
europepmc   +1 more source

Monitoring Atypical Metabolite Biomarkers in Patients with Bile Acid Synthesis Disorders by a Novel Targeted Tandem Mass Spectrometry Assay. [PDF]

Metabolites
Setchell KDR, Zhao X, Reed S, Zhang W.
europepmc   +1 more source

Tetrahedral framework nucleic acids ameliorate cholestatic liver disease by activating Wnt/β-catenin signaling and promoting ERK1/2 phosphorylation. [PDF]

Regen Biomater
Zhou J, Tang C, Song X, Wang Y, Lin B, Lin M, Xu Z, Lin S, Xu C, Yu C.   +9 more
europepmc   +1 more source

Significance of Genetic Testing in Diagnosing Cholestatic Disease in Infants. [PDF]

Cureus
Khan M, Shehzad MU, Khattak UM, Zeeshan N, Seerat I.   +4 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Transcriptional regulation of the human sterol 27-hydroxylase gene (CYP27) and promoter mapping

Atherosclerosis, 2001
Eran Leitersdorf, Alik Honigman, A Honigman   +2 more
exaly  

FXR-induced secretion of FGF15/19 inhibits CYP27 expression in cholangiocytes through p38 kinase pathway

Pflugers Archiv European Journal of Physiology, 2013
Heather Francis, David Moore, Xuefeng Xia   +2 more
exaly