Inventor
KEATING MARK T
US24 patents
⚠️ This page may combine multiple inventors who share the name “KEATING MARK T”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.
UNIV UTAH RES FOUND
22 patentsUS7125837B1Oct 24, 2006
Elastin-based compositions
UNIV UTAH RES FOUND15 citations92
US6787309B2Sep 7, 2004
Alterations in the long QT syndrome genes KVLQT1 and SCN5A and methods for detecting same
UNIV UTAH RES FOUND14 citations92
US6432644B1Aug 13, 2002
Mutations in the KCNE1 gene encoding human mink which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene
UNIV UTAH RES FOUND20 citations92
US6323026B1Nov 27, 2001
Mutations in the KCNE1 gene encoding human mink which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene
UNIV UTAH RES FOUND15 citations92
US6277978B1Aug 21, 2001
KVLQT1—a long QT syndrome gene
UNIV UTAH RES FOUND18 citations92
US6207383B1Mar 27, 2001
Mutations in and genomic structure of HERG—a long QT syndrome gene
UNIV UTAH RES FOUND25 citations92
US5599673AFeb 4, 1997
Long QT syndrome genes
UNIV UTAH RES FOUND46 citations92
US5650282AJul 22, 1997
Diagnosis of Williams syndrome
UNIV UTAH RES FOUND20 citations90
US7208273B2Apr 24, 2007
Common polymorphism in scn5a implicated in drug-induced cardiac arrhythmia
UNIV UTAH RES FOUND14 citations84
US6342357B1Jan 29, 2002
Alterations in the long QT syndrome genes KVLQT1 and SCN5A and methods for detecting same
UNIV UTAH RES FOUND11 citations74
US6150104ANov 21, 2000
Homozygous mutation in KVLQT1 which causes Jervell and Lange Nielsen syndrome
UNIV UTAH RES FOUND8 citations74
US6903244B1Jun 7, 2005
Mice which are +/− or −/− for the elastin gene as models for vascular disease
UNIV UTAH RES FOUND5 citations73
US6582913B1Jun 24, 2003
Diagnostic method for KVLQT1—a long QT syndrome gene
UNIV UTAH RES FOUND9 citations73
US6451534B1Sep 17, 2002
KVLQT1—a long QT syndrome gene
UNIV UTAH RES FOUND8 citations73
US6420124B1Jul 16, 2002
KVLQT1—a long qt syndrome gene
UNIV UTAH RES FOUND6 citations73
US6372958B1Apr 16, 2002
Transgenic mouse with endogenous endoglin gene disruption
UNIV UTAH RES FOUND10 citations73
US5858662AJan 12, 1999
Diagnosis of Williams syndrome and Williams syndrome cognitive profile by analysis of the presence or absence of a LIM-kinase gene
UNIV UTAH RES FOUND16 citations71
US6063576AMay 16, 2000
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
UNIV UTAH RES FOUND5 citations61
US5840489ANov 24, 1998
Diagnosis and treatment of supravalvular aortic stenosis and Williams syndrome
UNIV UTAH RES FOUND5 citations60
US6864364B1Mar 8, 2005
MinK-related genes, formation of potassium channels and association with cardiac arrhythmia
UNIV UTAH RES FOUND4 citations54
US7247436B2Jul 24, 2007
Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene
UNIV UTAH RES FOUND0 citations52
US7301067B2Nov 27, 2007
Mice which are +/− or −/− for the elastin gene as models for vascular disease
UNIV UTAH RES FOUND0 citations51