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Substrate and inhibitor specificity of class 1 and class 2 histone deacetylases

Journal of biotechnology, 2006-06, Vol.124 (1), p.258-270

2006

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An active site tyrosine residue is essential for amidohydrolase but not for esterase activity of a class 2 histone deacetylase-like bacterial enzyme

Biochemical journal, 2007-02, Vol.401 (3), p.659-665

2007

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Statistical Modeling of Interpersonal Distance with Range Imaging Data

Multimodal Signals: Cognitive and Algorithmic Issues, p.137-144

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Cation Radius Effects on Cell-Free Translation in Rabbit Reticulocyte Lysate

Biochemical and biophysical research communications, 2001-05, Vol.283 (2), p.267-272

2001

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Active site tyrosine is essential for amidohydrolase but not for esterase activity of a class 2 histone deacetylase-like bacterial enzyme

Biochemical journal, 2006-10, Vol.401 (3), p.659-665

2006

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A New Reporter Gene System Suited for Cell-Free Protein Synthesis and High-Throughput Screening in Small Reaction Volumes

Analytical biochemistry, 2001-10, Vol.297 (2), p.177-182

2001

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A Trans-amplifying RNA Vaccine Strategy for Induction of Potent Protective Immunity

Molecular therapy, 2020-01, Vol.28 (1), p.119-128

2020

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Activating Mutations in PAK1, Encoding p21-Activated Kinase 1, Cause a Neurodevelopmental Disorder

American journal of human genetics, 2018-10, Vol.103 (4), p.579-591

2018

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Phenotype in an Infant with SOD1 Homozygous Truncating Mutation

The New England journal of medicine, 2019-08, Vol.381 (5), p.486-488

2019

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Facile Bulk Synthesis of π‑Cubic SnS

Inorganic chemistry, 2017-10, Vol.56 (19), p.11455-11457

2017

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Design, simulation and experimental analysis of a monolithic bending section for enhanced maneuverability of single use laparoscopic devices

Scientific reports, 2024-02, Vol.14 (1), p.3309-3309

2024

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Defining clinical subgroups and genotype–phenotype correlations in NBAS-associated disease across 110 patients

Genetics in medicine, 2020-03, Vol.22 (3), p.610-621

2020

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Accessing the stapedius muscle via novel surgical retrofacial approach during cochlear implantation surgery: Intraoperative results on feasibility and safety

PloS one, 2022-08, Vol.17 (8), p.e0272943-e0272943

2022

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Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies

European journal of human genetics : EJHG, 2022-05, Vol.30 (5), p.611-618

2022

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Expanding the phenotypic and biochemical spectrum of NDUFAF3-related mitochondrial disease

Molecular genetics and metabolism, 2023-11, Vol.140 (3), p.107675-107675, Article 107675

2023

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Enhancing Charge Carrier Lifetime in Metal Oxide Photoelectrodes through Mild Hydrogen Treatment

Advanced energy materials, 2017-11, Vol.7 (22), p.n/a

2017

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Large-Grain Double Cation Perovskites with 18 μs Lifetime and High Luminescence Yield for Efficient Inverted Perovskite Solar Cells

ACS energy letters, 2021-03, Vol.6 (3), p.1045-1054

2021

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Carrier Localization on the Nanometer‐Scale limits Transport in Metal Oxide Photoabsorbers

Advanced functional materials, 2023-06, Vol.33 (25), p.n/a

2023

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Trans-amplifying RNA expressing functional miRNA mediates target gene suppression and simultaneous transgene expression

Molecular therapy. Nucleic acids, 2024-06, Vol.35 (2), p.102162-102162, Article 102162

2024

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Paralog Studies Augment Gene Discovery: DDX and DHX Genes

American journal of human genetics, 2019-08, Vol.105 (2), p.302-316

2019

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Recurrent acute liver failure in alanyl-tRNA synthetase-1 (AARS1) deficiency

Molecular genetics and metabolism reports, 2020-12, Vol.25, p.100681-100681, Article 100681

2020

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LYRM7 - associated complex III deficiency: A clinical, molecular genetic, MR tomographic, and biochemical study

Mitochondrion, 2017-11, Vol.37, p.55-61

2017

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Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy

American journal of human genetics, 2016-02, Vol.98 (2), p.358-362

2016

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Substrate and inhibitor specificity of class 1 and class 2 histone deacetylases

An active site tyrosine residue is essential for amidohydrolase but not for esterase activity of a class 2 histone deacetylase-like bacterial enzyme

Statistical Modeling of Interpersonal Distance with Range Imaging Data

Cation Radius Effects on Cell-Free Translation in Rabbit Reticulocyte Lysate

Active site tyrosine is essential for amidohydrolase but not for esterase activity of a class 2 histone deacetylase-like bacterial enzyme

A New Reporter Gene System Suited for Cell-Free Protein Synthesis and High-Throughput Screening in Small Reaction Volumes

A Trans-amplifying RNA Vaccine Strategy for Induction of Potent Protective Immunity

Activating Mutations in PAK1, Encoding p21-Activated Kinase 1, Cause a Neurodevelopmental Disorder

Phenotype in an Infant with SOD1 Homozygous Truncating Mutation

Facile Bulk Synthesis of π‑Cubic SnS

Design, simulation and experimental analysis of a monolithic bending section for enhanced maneuverability of single use laparoscopic devices

Defining clinical subgroups and genotype–phenotype correlations in NBAS-associated disease across 110 patients

Accessing the stapedius muscle via novel surgical retrofacial approach during cochlear implantation surgery: Intraoperative results on feasibility and safety

Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies

Expanding the phenotypic and biochemical spectrum of NDUFAF3-related mitochondrial disease

Enhancing Charge Carrier Lifetime in Metal Oxide Photoelectrodes through Mild Hydrogen Treatment

Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome

Large-Grain Double Cation Perovskites with 18 μs Lifetime and High Luminescence Yield for Efficient Inverted Perovskite Solar Cells

Carrier Localization on the Nanometer‐Scale limits Transport in Metal Oxide Photoabsorbers

Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiency

Trans-amplifying RNA expressing functional miRNA mediates target gene suppression and simultaneous transgene expression

Paralog Studies Augment Gene Discovery: DDX and DHX Genes

Recurrent acute liver failure in alanyl-tRNA synthetase-1 (AARS1) deficiency

LYRM7 - associated complex III deficiency: A clinical, molecular genetic, MR tomographic, and biochemical study

Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy

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