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/vufind/Search/Results?lookfor=%22Clemens%2C+Daniel+J%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Clemens%2C+Daniel+J%22&type=Person&sort=year
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PubPharm (9)
1
Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes
enthalten in:
Stem cell reports
| 2023
von
Clemens, D.
|
Ye, D.
|
Wang, L.
| +7
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2
SARS-CoV-2 spike protein-mediated cardiomyocyte fusion may contribute to increased arrhythmic risk in COVID-19
enthalten in:
PloS one
| 2023
von
Clemens, D.
|
Ye, D.
|
Zhou, W.
| +9
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3
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death Victims
enthalten in:
Circulation. Genomic and precision medicine
| 2020
von
Clemens, D.
|
Gray, B.
|
Bagnall, R.
| +9
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4
Phenotype-guided whole genome analysis in a patient with genetically elusive long QT syndrome yields a novel TRDN-encoded triadin pathogenetic substrate for triadin knockout syndrome and reveals a novel primate-specific cardiac TRDN transcript
enthalten in:
Heart rhythm
| 2020
von
Clemens, D.
|
Tester, D.
|
Marty, I.
| +1
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5
Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population
enthalten in:
Circulation. Genomic and precision medicine
| 2020
von
Clemens, D.
|
Gray, B.
|
Bagnall, R.
| +7
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6
Human Induced Pluripotent Stem Cell-Derived Non-Cardiomyocytes Modulate Cardiac Electrophysiological Maturation Through Connexin 43-Mediated Cell-Cell Interactions
enthalten in:
Stem cells and development
| 2020
von
Biendarra-Tiegs, S.
|
Clemens, D.
|
Secreto, F.
| +1
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7
Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome : Causative variants from pathogenic to likely benign
enthalten in:
Heart rhythm
| 2020
von
Mattivi, C.
|
Ye, D.
|
Tester, D.
| +4
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8
International Triadin Knockout Syndrome Registry
enthalten in:
Circulation. Genomic and precision medicine
| 2019
von
Clemens, D.
|
Tester, D.
|
Giudicessi, J.
| +16
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9
Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome type 1 mutations from pathogenic to benign
enthalten in:
Heart rhythm
| 2018
von
Clemens, D.
|
Lentino, A.
|
Kapplinger, J.
| +4
CommentIn: Heart Rhythm. 2018 Apr;15(4):562-563. - PMID 29317317
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1
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Circulation. Genomic and precision medicine
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1
PloS one
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Thema
9
Research Support, Non-U.S. Gov't
8
Journal Article
4
Arrhythmia
3
Carrier Proteins
3
Genetics
3
Muscle Proteins
3
Pediatrics
3
Research Support, N.I.H., Extramural
3
TRDN protein, human
3
genetics
3
pediatrics
2
9007-49-2
2
Calcium
2
DNA
2
Long QT syndrome
2
SY7Q814VUP
2
Triadin
2
death
2
long QT syndrome
2
phenotype
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Erscheinungszeitraum
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2020-
2
2010-2019
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