Results 121 to 130 of about 2,152 (193)

GLIS3, a novel regulator of eicosanoid gene expression and metabolism in normal kidney and polycystic kidney disease. [PDF]

Biochem Pharmacol
Srivastava C, Kang HS, Edin ML, Mukherjee T, Lih FB, Grimm SA, Collier JB, Zeldin DC, Jetten AM.   +8 more
europepmc   +1 more source

Mouse mammary stem cells express prognostic markers for triple-negative breast cancer [PDF]

, 2015

core   +1 more source

An environmentally relevant phthalate mixture impairs ovulatory prostaglandin and progesterone receptor pathways in human granulosa cells in vitro. [PDF]

Environ Int
Land KL, Xu H, Akin JW, Hannon PR.
europepmc   +1 more source

Correction to: Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbing

Pediatric Rheumatology Online Journal, 2023
Rafaela Nicolau, Tiago Beirão, Francisca Guimarães, Francisca Aguiar, Sara Ganhão, Mariana Rodrigues, Ana Grangeia, Iva Brito   +7 more
doaj   +1 more source

SLCO2A1 gene is the causal gene for both primary hypertrophic osteoarthropathy and hereditary chronic enteropathy

Journal of Orthopaedic Translation, 2021
Junji Umeno, Takayuki Matsumoto, Yuta Fuyuno, Motohiro Esaki, Takehiro Torisu   +4 more
doaj   +1 more source

Cryptogenic multifocal ulcerative stenosing enteritis (CMUSE): a rare case and a review of the literature. [PDF]

J Surg Case Rep
Hudson L, Grayson N, Toomey D.
europepmc   +1 more source

Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review. [PDF]

Cureus
Mohammad M, Alnajjar Y, Jondi E, Alsheikh M, Darras A, Hamamdah A, Itmaizeh M.   +6 more
europepmc   +1 more source

Transporter gene expression in human head and neck squamous cell carcinoma and associated epigenetic regulatory mechanisms [PDF]

, 2013
Fromm, Martin F., Iro, Heinrich, Muschler, Marc, Schnepf, Rebecca, Traxdorf, Maximilian, Wendler, Olaf, Zenk, Johannes, Zolk, Oliver   +7 more
core   +1 more source

Genotype-Phenotype Correlation Insights in a Rare Case Presenting with Multiple Osteodysplastic Syndromes. [PDF]

Genes (Basel)
Yapijakis C, Gintoni I, Chamakioti M, Koniari E, Papanikolaou E, Kassi E, Vlachakis D, Chrousos GP.   +7 more
europepmc   +1 more source

Distinct features of three clinical subtypes in 533 patients with primary hypertrophic osteoarthropathy. [PDF]

Orphanet J Rare Dis
Cai X, Yang X, Zhang P, Dou Z, Chen Z, Zhu C, Xu W, Wang X, Hong X, Zhang Z.   +9 more
europepmc   +1 more source