Huntington's gene: so near, yet so far

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

The visual brain hypothesis.

Science (New York, N.Y.)·2026

Listening to storms as they shake Earth.

Science (New York, N.Y.)·2026

AI-designed viral genomes.

Science (New York, N.Y.)·2026

A fungus makes itself at home on skin.

Science (New York, N.Y.)·2026

The next Turing tests: Reimagining conceptions and measures of AI.

Science (New York, N.Y.)·2026

Paleogenomic insight into the collapse, recovery, and management of American bison.

Science (New York, N.Y.)·2026

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Frontiers in genetics·2026

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

Frontiers in pediatrics·2026

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Seizure·2026

Related Experiment Videos

Huntington's gene: so near, yet so far

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.

The visual brain hypothesis.

Listening to storms as they shake Earth.

AI-designed viral genomes.

A fungus makes itself at home on skin.

The next Turing tests: Reimagining conceptions and measures of AI.

Paleogenomic insight into the collapse, recovery, and management of American bison.

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Related Experiment Videos

Huntington's gene: so near, yet so far

Related Concept Videos

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