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Cancer Research|May 19, 2006
Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United KingdomZoe E Kemp, Luis G Carvajal-Carmona, Ella Barclay, et al.
Heart Rhythm|May 8, 2024
The spatial ventricular gradient is associated with inducibility of ventricular arrhythmias during electrophysiology studyNicolas Isaza, Hans F Stabenau, Daniel B Kramer, et al.
Investigative Ophthalmology & Visual Science|May 26, 2005
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) familiesNeil D Ebenezer, Michel Michaelides, Sharon A Jenkins, et al.
Anticancer Research|December 25, 2009
Mutation analysis of hypoxia-inducible factors HIF1A and HIF2A in renal cell carcinomaMark R Morris, David J Hughes, Ya-Min Tian, et al.
BMJ Open|November 6, 2020
Ensuring that COVID-19 research is inclusive: guidance from the NIHR INCLUDE projectMiles D Witham, Eleanor Anderson, Camille B Carroll, et al.
The Journal of Innovations in Cardiac Rhythm Management|July 16, 2024
Utility of an Externalized Temporary Transvenous Implantable Cardioverter-defibrillator System in the Setting of Ventricular Tachycardia Storm and Concurrent Device Infection Requiring ExtractionRonuk M Modi, Marianna Lozano Cruz Marquez, Shu Yang, et al.
The Lancet. Child & Adolescent Health|January 23, 2021
Predisposition to cancer in children and adolescentsChristian P Kratz, Marjolijn C Jongmans, Hélène Cavé, et al.
Molecular and Cellular Biology|June 25, 2008
Chaperone Hsp27, a novel subunit of AUF1 protein complexes, functions in AU-rich element-mediated mRNA decayKristina S Sinsimer, Frances M Gratacós, Anna M Knapinska, et al.
The Journal of Clinical Investigation|May 30, 2009
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystoniaManju A Kurian, Juan Zhen, Shu-Yuan Cheng, et al.
Human Molecular Genetics|June 9, 1998
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5M Paulsen, K R Davies, L M Bowden, et al.
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