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Journal of infectious pulmonary diseases·2018

Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk.

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Methods in molecular biology (Clifton, N.J.)·2011

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility.

Diabetologia·2010

Lymphocyte subpopulations and intima media thickness in primary antiphospholipd syndrome.

Lupus·2005

An intrinsically disordered domain of transcription terminator Rho governs genome-wide Rho utilization (Rut) site selection in Mycobacterium tuberculosis.

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Wavelet-based whole genome doubling aware single-cell copy number calling.

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Nucleic acids research·2026

HLH-30/TFEB is necessary for chromatin reorganization and maintenance of cell quiescence during starvation in C. elegans.

Nucleic acids research·2026

Cell cycle-dependent chromatin motion: a role for DNA content doubling over cohesion.

Nucleic acids research·2026

Dosimetry validation via EGS5 Monte Carlo simulation, microbial inactivation kinetics, and quality preservation of frozen sliced squid (Loligo spp.) under 10 MeV electron beam irradiation.

Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine·2026

Second-Generation Acyl Modifications Stabilize RNA, Support Translation, and Suppress Cytokine Responses.

ACS chemical biology·2026

Switching ATP-Forming Phosphoryl-Transfer Chemistry With a Restricted Set of Amino Acids.

Angewandte Chemie (International ed. in English)·2026

Cooperative Fe-LMCT and Ni-SH2 Catalysis for Native Carboxylic Acid Methyl Editing.

Angewandte Chemie (International ed. in English)·2026

Correction to "Activity of Amorphous NiB/SiO2 in Hydrotreating Model Reactions: Hydrodesulfurization of 4,6-DMDBT".

ACS omega·2026

Mn/Fe synergy enables wide-temperature NH3-SCR activity over MnFeCe/SSZ-13: insights into the structure-activity relationship.

RSC advances·2026

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Cystic Fibrosis Mice Develop Spontaneous Chronic Bordetella Airway Infections.

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A role for coding functional variants in HNF4A in type 2 diabetes susceptibility.

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