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Spectroscopic and thermodynamic characterization of a cobalt-verdazyl valence tautomeric system. influence of crystal structure, solvent and counterion

Dalton transactions : an international journal of inorganic chemistry, 2024-04, Vol.53 (17), p.7536-7545

2024

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Splicing in two skeletal muscle transcripts correlates with clinical phenotype in myotonic dystrophy type 1 patients

Journal of neurology, 2022-05, Vol.269 (5), p.2784-2787

2022

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Long-range spin dependent delocalization promoted by the pseudo Jahn-Teller effect

The Journal of chemical physics, 2019-11, Vol.151 (20), p.201103-201103

2019

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α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

Human molecular genetics, 2010-10, Vol.19 (20), p.4007-4016

2010

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Quantitative Methods to Monitor RNA Biomarkers in Myotonic Dystrophy

Scientific reports, 2018-04, Vol.8 (1), p.5885-13, Article 5885

2018

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The miR-30 microRNA family targets smoothened to regulate hedgehog signalling in zebrafish early muscle development

PloS one, 2013-06, Vol.8 (6), p.e65170-e65170

2013

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Global Increase in Circular RNA Levels in Myotonic Dystrophy

Frontiers in genetics, 2019-07, Vol.10, p.649-649

2019

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Correction: An electron transfer driven magnetic switch: ferromagnetic exchange and spin delocalization in iron verdazyl complexes

Dalton transactions : an international journal of inorganic chemistry, 2018-06, Vol.47 (24), p.8164-8164

2018

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T-box genes in human disorders

Human molecular genetics, 2003-04, Vol.12 (suppl-1), p.R37-R44

2003

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A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20

Human molecular genetics, 2016-06, Vol.25 (11), p.2331-2341

2016

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Metal-ligand interactions in a redox active ligand system. Electrochemistry and spectroscopy of [M(dipyvd)2]n+ (M=Zn, Ni, n=0, 1, 2)

Frontiers in chemistry, 2023-11, Vol.11, p.1295289-1295289

2023

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Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

Genome medicine, 2020-08, Vol.12 (1), p.76-13, Article 76

2020

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Structure−Property Relationships of Stable Free Radicals: Verdazyls with Electron-Rich Aryl Substituents

Journal of organic chemistry, 2009-03, Vol.74 (5), p.1850-1857

2009

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Modifications of Tanabe-Sugano d6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Inorganic chemistry, 2023-04, Vol.62 (14), p.5737-5743

2023

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Modifications of Tanabe-Sugano d 6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Inorganic chemistry, 2023-04, Vol.62 (14), p.5737-5743

2023

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Recent advances in congenital heart disease genomics

F1000 research, 2017, Vol.6, p.869-869

2017

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Body composition and clinical outcome measures in patients with myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2017-03, Vol.27 (3), p.286-289

2017

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Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart

Journal of anatomy, 2024-07, Vol.245 (1), p.70-83

2024

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Acetylation of TBX5 by KAT2B and KAT2A regulates heart and limb development

Journal of molecular and cellular cardiology, 2018-01, Vol.114, p.185-198

2018

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Knockdown of alpha myosin heavy chain disrupts the cytoskeleton and leads to multiple defects during chick cardiogenesis

Journal of anatomy, 2009-06, Vol.214 (6), p.905-915

2009

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HDAC4 and 5 repression of TBX5 is relieved by protein kinase D1

Scientific reports, 2019-11, Vol.9 (1), p.17992-10, Article 17992

2019

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Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts

Human genetics, 2006-11, Vol.120 (4), p.487-499

2006

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Zebrafish deficient for Muscleblind-like 2 exhibit features of myotonic dystrophy

Disease models & mechanisms, 2011-05, Vol.4 (3), p.381-392

2011

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Suzuki–Miyaura Coupling of Verdazyl Radicals

European journal of organic chemistry, 2017-02, Vol.2017 (7), p.1125-1131

2017

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Spectroscopic and thermodynamic characterization of a cobalt-verdazyl valence tautomeric system. influence of crystal structure, solvent and counterion

Splicing in two skeletal muscle transcripts correlates with clinical phenotype in myotonic dystrophy type 1 patients

Long-range spin dependent delocalization promoted by the pseudo Jahn-Teller effect

α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

Quantitative Methods to Monitor RNA Biomarkers in Myotonic Dystrophy

The miR-30 microRNA family targets smoothened to regulate hedgehog signalling in zebrafish early muscle development

Global Increase in Circular RNA Levels in Myotonic Dystrophy

Correction: An electron transfer driven magnetic switch: ferromagnetic exchange and spin delocalization in iron verdazyl complexes

T-box genes in human disorders

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20

Metal-ligand interactions in a redox active ligand system. Electrochemistry and spectroscopy of [M(dipyvd)2]n+ (M=Zn, Ni, n=0, 1, 2)

Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

Structure−Property Relationships of Stable Free Radicals: Verdazyls with Electron-Rich Aryl Substituents

Modifications of Tanabe-Sugano d6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Modifications of Tanabe-Sugano d 6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Recent advances in congenital heart disease genomics

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

Body composition and clinical outcome measures in patients with myotonic dystrophy type 1

Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart

Acetylation of TBX5 by KAT2B and KAT2A regulates heart and limb development

Knockdown of alpha myosin heavy chain disrupts the cytoskeleton and leads to multiple defects during chick cardiogenesis

HDAC4 and 5 repression of TBX5 is relieved by protein kinase D1

Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts

Zebrafish deficient for Muscleblind-like 2 exhibit features of myotonic dystrophy

Suzuki–Miyaura Coupling of Verdazyl Radicals

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