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Deletion of Tmtc4 activates the unfolded protein response and causes postnatal hearing loss

The Journal of clinical investigation, 2018-11, Vol.128 (11), p.5150-5162

2018

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TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function

Nature communications, 2023-12, Vol.14 (1), p.8111-8111, Article 8111

2023

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Synaptic ribbon dynamics after noise exposure in the hearing cochlea

Communications biology, 2024-04, Vol.7 (1), p.421-421

2024

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Racial and ethnic disparities in diagnostic efficacy of comprehensive genetic testing for sensorineural hearing loss

Human genetics, 2022-04, Vol.141 (3-4), p.495-504

2022

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Integrated stress response inhibition provides sex-dependent protection against noise-induced cochlear synaptopathy

Scientific reports, 2020-10, Vol.10 (1), p.18063, Article 18063

2020

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Identification of maximal steady-state metabolic rate by the change in muscle oxygen saturation

Journal of applied physiology (1985), 2023-06, Vol.134 (6), p.1349-1358

2023

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Radical deoxygenation of 3-azatricyclo[2.2.1.0 2,6]heptan-5-ols to 2-azabicyclo[2.2.1]hept-5-enes and 1,2-dihydropyridines

Tetrahedron, 2009-09, Vol.65 (37), p.7825-7836

2009

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The effect of carbon fiber plated shoes on submaximal running mechanics in non-elite runners

Footwear science, 2023-09, Vol.15 (3), p.171-177

2023

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TMTC4 is a hair cell-specific human deafness gene

JCI insight, 2023-12, Vol.8 (24)

2023

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Effects of rituximab on lymphocytes in multiple sclerosis and neuromyelitis optica

Multiple sclerosis and related disorders, 2014-03, Vol.3 (2), p.244-252

2014

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Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

Angewandte Chemie (International ed.), 2002-11, Vol.41 (22), p.4313-4316

2002

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Synthesis of the heptacyclic indole alkaloid (.+-.)-kopsine and related studies

Journal of the American Chemical Society, 1989-08, Vol.111 (17), p.6707-6711

1989

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6-Substituted 2-azabicyclo[2.2.1]hept-5-enes by nitrogen-directed radical rearrangement: synthesis of an epibatidine analogue with high binding affinity at the nicotinic acetylcholine receptorElectronic supplementary information (ESI) available: details of biological studies. See http://www.rsc.org/suppdata/p1/b1/b107414h

Perkin 1 : an international journal of organic and bio-organic chemistry, 2001-11 (23), p.3150-3158

2001

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Organolithium-induced enantioselective alkylative double ring-opening of epoxides: synthesis of enantioenriched unsaturated amino alcohols

Tetrahedron, 2004-04, Vol.60 (16), p.3611-3624

2004

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Synthesis of the hexacyclic indole alkaloid (.+-.)-kopsijasmine

Journal of organic chemistry, 1988-11, Vol.53 (24), p.5772-5776

1988

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Radical Deoxygenation of 3-Azatricyclo[2.2.1.02,6]heptan-5-ols to 1,2-Dihydropyridines

Synlett, 2005-02, Vol.2005 (2), p.325-327

2005

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High-Affinity Small Molecule Inhibitors of T Cell Costimulation: Compounds for Immunotherapy

Chemistry & biology, 2004-12, Vol.11 (12), p.1651-1658

2004

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An Epoxide Rearrangement - Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue

Synlett, 1998-12, Vol.1998 (12), p.1349-1350

1998

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Asymmetric rearrangement of N-Boc 7-azanorbornene oxide: use of aryllithiums for enantioselective deprotonation

Tetrahedron: asymmetry, 1999-05, Vol.10 (10), p.1847-1850

1999

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Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

Angewandte Chemie (International ed.), 2002-12, Vol.41 (24), p.4611-4611

2002

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Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

Angewandte Chemie, 2002-12, Vol.114 (24), p.4806-4806

2002

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Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

Angewandte Chemie, 2002-11, Vol.114 (22), p.4489-4492

2002

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W11. GENOME-WIDE ANALYSIS OF THE ANXIETY DISORDER SPECTRUM

European neuropsychopharmacology, 2021-10, Vol.51, p.e152-e153

2021

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ChemInform Abstract: An Epoxide Rearrangement - Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue

ChemInform, 1999-04, Vol.30 (14), p.no-no

1999

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ChemInform Abstract: 6-Substituted 2-Azabicyclo[2.2.1]hept-5-enes by Nitrogen-Directed Radical Rearrangement: Synthesis of an Epibatidine Analogue (VIII) with High Binding Affinity at the Nicotinic Acetylcholine Receptor

ChemInform, 2002-04, Vol.33 (14), p.no-no

2002

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Deletion of Tmtc4 activates the unfolded protein response and causes postnatal hearing loss

TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function

Synaptic ribbon dynamics after noise exposure in the hearing cochlea

Racial and ethnic disparities in diagnostic efficacy of comprehensive genetic testing for sensorineural hearing loss

Integrated stress response inhibition provides sex-dependent protection against noise-induced cochlear synaptopathy

Identification of maximal steady-state metabolic rate by the change in muscle oxygen saturation

Radical deoxygenation of 3-azatricyclo[2.2.1.0 2,6]heptan-5-ols to 2-azabicyclo[2.2.1]hept-5-enes and 1,2-dihydropyridines

The effect of carbon fiber plated shoes on submaximal running mechanics in non-elite runners

TMTC4 is a hair cell-specific human deafness gene

Effects of rituximab on lymphocytes in multiple sclerosis and neuromyelitis optica

Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

Synthesis of the heptacyclic indole alkaloid (.+-.)-kopsine and related studies

Organolithium-induced enantioselective alkylative double ring-opening of epoxides: synthesis of enantioenriched unsaturated amino alcohols

Synthesis of the hexacyclic indole alkaloid (.+-.)-kopsijasmine

Radical Deoxygenation of 3-Azatricyclo[2.2.1.02,6]heptan-5-ols to 1,2-Dihydropyridines

High-Affinity Small Molecule Inhibitors of T Cell Costimulation: Compounds for Immunotherapy

An Epoxide Rearrangement - Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue

Asymmetric rearrangement of N-Boc 7-azanorbornene oxide: use of aryllithiums for enantioselective deprotonation

Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

W11. GENOME-WIDE ANALYSIS OF THE ANXIETY DISORDER SPECTRUM

ChemInform Abstract: An Epoxide Rearrangement - Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue

ChemInform Abstract: 6-Substituted 2-Azabicyclo[2.2.1]hept-5-enes by Nitrogen-Directed Radical Rearrangement: Synthesis of an Epibatidine Analogue (VIII) with High Binding Affinity at the Nicotinic Acetylcholine Receptor

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