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The Biochemical Journal|March 7, 2012
Feedback regulation by Atf3 in the endothelin-1-responsive transcriptome of cardiomyocytes: Egr1 is a principal Atf3 targetAlejandro Giraldo, Oliver P T Barrett, Marcus J Tindall, et al.
Oncogene|October 10, 2012
Anti-tumorigenic effects of Type 1 interferon are subdued by integrated stress responsesS Bhattacharya, W-C HuangFu, G Dong, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 21, 2014
A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosisM W Konstan, G Döring, S L Heltshe, et al.
Annals of the Royal College of Surgeons of England|September 24, 2016
Complications of biliary-enteric anastomosesR S Kadaba, K A Bowers, S Khorsandi, et al.
Advanced Materials (Deerfield Beach, Fla.)|November 16, 2022
High Entropy Approach to Engineer Strongly Correlated Functionalities in ManganitesAbhishek Sarkar, Di Wang, Mohana V Kante, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|February 23, 2026
Time-series Machine Learning Models to Support Emergency Department Operational PlanningTamanna T K Munia, Kyle Marshall, Kitae Kim, et al.
Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.
Mutation Research|April 19, 2011
Low dose radiation response curves, networks and pathways in human lymphoblastoid cells exposed from 1 to 10cGy of acute gamma radiationA J Wyrobek, C F Manohar, V V Krishnan, et al.
Genome Research|November 1, 1996
Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mappingD L Thiselton, R M Hampson, M Nayudu, et al.
Human Genetics|December 1, 1991
Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophyK M Bushby, N J Cleghorn, A Curtis, et al.
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