Screening for polymorphisms in exon 5 of the glutathione S-transferase P1 gene

Cellular aspects of vascular remodeling in hypertension revealed by confocal microscopy.

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Osteoarticular and muscle infectious lesions in patients with the human immunodeficiency virus.

Clinical rheumatology·1997

Carbon monoxide inhibits hypoxic pulmonary vasoconstriction in rats by a cGMP-independent mechanism.

Pflugers Archiv : European journal of physiology·1997

NMR solution structure of the 205-316 C-terminal fragment of thermolysin. An example of dimerization coupled to partial unfolding.

Biochemistry·1997

Neuronal nitric oxide synthase activation by vasoactive intestinal peptide in bovine cerebral arteries.

Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism·1997

Long-term extractable compounds screening in surface water to prevent accidental organic pollution.

The Science of the total environment·1997

End of rarity: the evolving burden of interstitial lung diseases in England - trends from a national population-based cohort study.

Thorax·2026

Stakeholder-informed prioritisation of HealthTech innovation across chronic respiratory disease: the HERON study.

Thorax·2026

PM2.5, O3 and survival gains from China's clean air actions among patients with lung cancer: a 20-year registry-based cohort study in Beijing.

Thorax·2026

Effects of obstructive sleep apnoea treatment on cardiovascular and sleep health in bed partners: the sleep partners clinical trial.

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Systematic misclassification of lung function in Indian adolescents using GLI-2012 reference equations: evidence from the multicity APEAL cohort.

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International epidemiology of antimicrobial resistance in people living with chronic lung infection.

Thorax·2026

Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Vavilovskii zhurnal genetiki i selektsii·2026

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

Frontiers in endocrinology·2026

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

Vavilovskii zhurnal genetiki i selektsii·2026

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Genome research·2026

Genetic Susceptibility in Relative Maternal Protection From Type 1 Diabetes.

Diabetes care·2026

Deciphering pervasive domestication and active "dark matter" of proviruses in prokaryotes via precision border mapping.

Science advances·2026

Related Experiment Videos

Screening for polymorphisms in exon 5 of the glutathione S-transferase P1 gene

Related Concept Videos

Cellular aspects of vascular remodeling in hypertension revealed by confocal microscopy.

Osteoarticular and muscle infectious lesions in patients with the human immunodeficiency virus.

Carbon monoxide inhibits hypoxic pulmonary vasoconstriction in rats by a cGMP-independent mechanism.

NMR solution structure of the 205-316 C-terminal fragment of thermolysin. An example of dimerization coupled to partial unfolding.

Neuronal nitric oxide synthase activation by vasoactive intestinal peptide in bovine cerebral arteries.

Long-term extractable compounds screening in surface water to prevent accidental organic pollution.

End of rarity: the evolving burden of interstitial lung diseases in England - trends from a national population-based cohort study.

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Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.

Case Report: A novel 1, 171 bp GCK promoter/exon 1 deletion in a Chinese pedigree: correcting a misdiagnosis of MODY10 based on an incidental INS variant.

A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.

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Screening for polymorphisms in exon 5 of the glutathione S-transferase P1 gene

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