Genetic evidence for CFTR dysfunction in Japanese: background for chronic pancreatitis

Cloning of a cDNA encoding the Tcp-1 (t complex polypeptide 1) homologue of Arabidopsis thaliana.

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The primary structure of porcine aminoacylase 1 deduced from cDNA sequence.

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Crystal structure of papain-succinyl-Gln-Val-Val-Ala-Ala-p-nitroanilide complex at 1.7-A resolution: noncovalent binding mode of a common sequence of endogenous thiol protease inhibitors.

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A point mutation of low-density-lipoprotein receptor causing rapid degradation of the receptor.

European journal of biochemistry·1992

Initial clinical experience with a single pass VDDR pacing system.

Pacing and clinical electrophysiology : PACE·1992

Crystallization and preliminary X-ray study of the cathepsin B complexed with CA074, a selective inhibitor.

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BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

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Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

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The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.

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Recent advances in etiology and treatment of von Hippel-Lindau Disease (VHLD).

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Ethical Issues Raised by Interventions to Prevent or Treat Childhood Obesity: A Systematic Qualitative Review.

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Dynamic feedback between IL-6 and TWIST1 drives pancreatic cancer progression.

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Bioinformatics advances·2026

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Genetic evidence for CFTR dysfunction in Japanese: background for chronic pancreatitis

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Cloning of a cDNA encoding the Tcp-1 (t complex polypeptide 1) homologue of Arabidopsis thaliana.

The primary structure of porcine aminoacylase 1 deduced from cDNA sequence.

Crystal structure of papain-succinyl-Gln-Val-Val-Ala-Ala-p-nitroanilide complex at 1.7-A resolution: noncovalent binding mode of a common sequence of endogenous thiol protease inhibitors.

A point mutation of low-density-lipoprotein receptor causing rapid degradation of the receptor.

Initial clinical experience with a single pass VDDR pacing system.

Crystallization and preliminary X-ray study of the cathepsin B complexed with CA074, a selective inhibitor.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Evolving roles within the genomic medicine workforce: a revised framework for UK practice-position on behalf of the Association of Genetic Nurses and Counsellors and the Clinical Genetics Society.

Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank.

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

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Genetic evidence for CFTR dysfunction in Japanese: background for chronic pancreatitis

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