Pharmacological aspects of physical dependence on ethanol

Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?

BJOG : an international journal of obstetrics and gynaecology·2021

A catalog of associations between rare coding variants and COVID-19 outcomes.

medRxiv : the preprint server for health sciences·2021

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Clinical genetics·2015

Practical considerations in the clinical application of whole-exome sequencing.

Clinical genetics·2015

The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome.

Clinical genetics·2014

Guidelines for investigating causality of sequence variants in human disease.

Nature·2014

Organ crosstalk in kidney diseases: Insights from metabolic, hormonal and nervous regulation.

Life sciences·2026

Melatonin system integrity shapes gut-brain interaction in schizophrenia-derived microbiota transplant phenotype in mice.

Life sciences·2026

SARS-CoV-2 nucleocapsid protein drives pulmonary injury by enhancing GRP75-dependent ER-mitochondria tethering and reprogramming of alveolar macrophages.

Life sciences·2026

MiR-485-5p targets RGS4 to promote angiogenesis in lower limb ischemia by activating VEGFR-2/AKT/ERK1/2 signaling.

Life sciences·2026

Calpain-2 inhibition prevents pressure overload-induced lysosomal cathepsin release and cardiac hypertrophy.

Life sciences·2026

Organelle contact sites as spatial regulators of lipid fate in adipose tissue metabolic disease.

Life sciences·2026

Exploring the Interface of Hyperconjugation and PolarizabilityEnhancing Pedagogies for Charge Stabilization in Organic Chemistry.

Journal of chemical education·2026

Water vapor oxidation behavior of high-entropy (Ti,Nb,Ta,Hf,W)C x at 1200 °C: the role of carbon vacancies.

RSC advances·2026

Cellular crosstalk between endothelial and vascular smooth muscle cells via the BACH1/COL3A1 axis promotes vascular calcification in chronic kidney disease.

Inflammation research : official journal of the European Histamine Research Society ... [et al.]·2026

Endothelial Calcium Dysregulation as an Early Trigger of Vascular Dysfunction: Insights into Heavy Metal Toxicity : Heavy Metals and Endothelial Ca2+ Dysregulation.

Handbook of experimental pharmacology·2026

Deciphering the stabilization mechanism of L-arginine and glycyl-L-arginine in an imidazolium-based ionic liquid through thermodynamic and computational approaches.

Physical chemistry chemical physics : PCCP·2026

Sodium-Induced Lipid Bilayer Phase Transition for an Ester Lipid and Phase Transition Resistance for an Ether Branched-Lipid.

Chemistry and physics of lipids·2026

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Pharmacological aspects of physical dependence on ethanol

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Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?

A catalog of associations between rare coding variants and COVID-19 outcomes.

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Practical considerations in the clinical application of whole-exome sequencing.

The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome.

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Cellular crosstalk between endothelial and vascular smooth muscle cells via the BACH1/COL3A1 axis promotes vascular calcification in chronic kidney disease.

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