Ethical questions haunt new genetic technologies

Epidemiological survey of Angiostrongylus vasorum in dogs and slugs around a new endemic focus in Scotland.

The Veterinary record·2015

Trends in door-to-balloon time and outcomes following primary percutaneous coronary intervention for ST-elevation myocardial infarction: an Australian perspective.

Internal medicine journal·2014

Breast cancer risk assessment in 8,824 women attending a family history evaluation and screening programme.

Familial cancer·2013

Mammographic surveillance in women aged 35-39 at enhanced familial risk of breast cancer (FH02).

Familial cancer·2013

Nutrition self-efficacy assessment: development of a questionnaire and evaluation of reliability in African-American and Latino children.

Journal of human nutrition and dietetics : the official journal of the British Dietetic Association·2013

Exploitation of interspecific diversity for monocot crop improvement.

Heredity·2013

Antibodies sculpt adult brain circuits.

Science (New York, N.Y.)·2026

Ice as a geochemical reactor.

Science (New York, N.Y.)·2026

To eat or to breathe?

Science (New York, N.Y.)·2026

Roots navigate around decay regions by sensing local pH gradients.

Science (New York, N.Y.)·2026

In Science Journals.

Science (New York, N.Y.)·2026

Transient assembly of precision-tuned platinum-skin intermetallic catalysts for fuel cells.

Science (New York, N.Y.)·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

Related Experiment Videos

Ethical questions haunt new genetic technologies

Related Concept Videos

Epidemiological survey of Angiostrongylus vasorum in dogs and slugs around a new endemic focus in Scotland.

Trends in door-to-balloon time and outcomes following primary percutaneous coronary intervention for ST-elevation myocardial infarction: an Australian perspective.

Breast cancer risk assessment in 8,824 women attending a family history evaluation and screening programme.

Mammographic surveillance in women aged 35-39 at enhanced familial risk of breast cancer (FH02).

Nutrition self-efficacy assessment: development of a questionnaire and evaluation of reliability in African-American and Latino children.

Exploitation of interspecific diversity for monocot crop improvement.

Antibodies sculpt adult brain circuits.

Ice as a geochemical reactor.

To eat or to breathe?

Roots navigate around decay regions by sensing local pH gradients.

In Science Journals.

Transient assembly of precision-tuned platinum-skin intermetallic catalysts for fuel cells.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Related Experiment Videos

Ethical questions haunt new genetic technologies

Related Concept Videos

Related Articles