proline and Long QT Syndrome 1

proline has been researched along with Long QT Syndrome 1 in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Brockmeier, K; Karle, CA; Katus, HA; Khalil, M; Kiehn, J; Koenen, M; Kreye, VA; Licka, M; Schoels, W; Thomas, D; Ulmer, HE; Wimmer, AB; Wu, K; Zehelein, J	1
Bafunno, V; Brunetti, ND; Di Biase, M; Grimaldi, M; Ieva, R; Margaglione, M; Mavilio, G; Pellegrino, PL; Sessa, F	1

Other Studies

2 other study(ies) available for proline and Long QT Syndrome 1

Article	Year
Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome. Biochimica et biophysica acta, 2004, Nov-05, Volume: 1690, Issue:3 Topics: Amino Acid Sequence; Animals; Base Sequence; Cloning, Molecular; DNA Mutational Analysis; Electrophysiology; Female; Gene Expression; Humans; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Male; Molecular Sequence Data; Mutation; Oocytes; Patch-Clamp Techniques; Pedigree; Phenotype; Polymorphism, Single-Stranded Conformational; Potassium; Potassium Channels, Voltage-Gated; Proline; Romano-Ward Syndrome; Sequence Alignment; Xenopus laevis	2004
A novel mutation in human ether-a-go-go-related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT syndrome. The American journal of cardiology, 2007, Jun-15, Volume: 99, Issue:12 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Electrocardiography; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Genes, Dominant; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Proline; Romano-Ward Syndrome	2007

Article

Year

Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome.

Biochimica et biophysica acta, 2004, Nov-05, Volume: 1690, Issue:3

Topics: Amino Acid Sequence; Animals; Base Sequence; Cloning, Molecular; DNA Mutational Analysis; Electrophysiology; Female; Gene Expression; Humans; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Male; Molecular Sequence Data; Mutation; Oocytes; Patch-Clamp Techniques; Pedigree; Phenotype; Polymorphism, Single-Stranded Conformational; Potassium; Potassium Channels, Voltage-Gated; Proline; Romano-Ward Syndrome; Sequence Alignment; Xenopus laevis

2004

A novel mutation in human ether-a-go-go-related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT syndrome.

The American journal of cardiology, 2007, Jun-15, Volume: 99, Issue:12

Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Electrocardiography; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Genes, Dominant; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Proline; Romano-Ward Syndrome

2007