Three MspI polymorphisms at the UGT1 locus

Same author

Clinical and electroencephalographic findings in acutely ill adults with non-convulsive vs convulsive status epilepticus.

Acta neurologica Scandinavica·2014

Same author

Pulmonary vascular disease in Gaucher disease: clinical spectrum, determinants of phenotype and long-term outcomes of therapy.

Journal of inherited metabolic disease·2011

Same author

Impact of a real-time peer review audit on patient management in a radiation oncology department.

Journal of medical imaging and radiation oncology·2009

Same author

17beta-hydroxysteroid dehydrogenases: physiological roles in health and disease.

Trends in endocrinology and metabolism: TEM·2008

Same author

CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families.

The British journal of dermatology·2005

Same author

A germline mutation in KIT in familial diffuse cutaneous mastocytosis.

Journal of medical genetics·2004

Same journal

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Human molecular genetics·2026

Same journal

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Human molecular genetics·2026

Same journal

Nicotinamide riboside prevents mitochondrial dysfunction in nemaline myopathy type 6.

Human molecular genetics·2026

Same journal

Retraction: Aqua-soluble DDQ reduces the levels of Dr1 and Ab and inhibits abnormal interactions between Ab and Dr1 and protects Alzheimer's disease neurons from Ab- and Dr1-induced mitochondrial and synaptic toxicities.

Human molecular genetics·2026

Same journal

Retraction: Breast cancer cell-derived exosome-delivered microRNA-155 targets UBQLN1 in adipocytes and facilitates cancer cachexia-related fat loss.

Human molecular genetics·2026

Same journal

Editor's Note: Protective effects of antidepressant citalopram against abnormal APP processing and amyloid beta-induced mitochondrial dynamics, biogenesis, mitophagy and synaptic toxicities in Alzheimer's disease.

Human molecular genetics·2026

Related Experiment Videos

Three MspI polymorphisms at the UGT1 locus

Related Concept Videos

Clinical and electroencephalographic findings in acutely ill adults with non-convulsive vs convulsive status epilepticus.

Pulmonary vascular disease in Gaucher disease: clinical spectrum, determinants of phenotype and long-term outcomes of therapy.

Impact of a real-time peer review audit on patient management in a radiation oncology department.

17beta-hydroxysteroid dehydrogenases: physiological roles in health and disease.

CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families.

A germline mutation in KIT in familial diffuse cutaneous mastocytosis.

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Nicotinamide riboside prevents mitochondrial dysfunction in nemaline myopathy type 6.

Retraction: Aqua-soluble DDQ reduces the levels of Dr1 and Ab and inhibits abnormal interactions between Ab and Dr1 and protects Alzheimer's disease neurons from Ab- and Dr1-induced mitochondrial and synaptic toxicities.

Retraction: Breast cancer cell-derived exosome-delivered microRNA-155 targets UBQLN1 in adipocytes and facilitates cancer cachexia-related fat loss.

Editor's Note: Protective effects of antidepressant citalopram against abnormal APP processing and amyloid beta-induced mitochondrial dynamics, biogenesis, mitophagy and synaptic toxicities in Alzheimer's disease.

Related Experiment Videos

Three MspI polymorphisms at the UGT1 locus

Related Concept Videos

Related Articles

Clinical and electroencephalographic findings in acutely ill adults with non-convulsive vs convulsive status epilepticus.

Pulmonary vascular disease in Gaucher disease: clinical spectrum, determinants of phenotype and long-term outcomes of therapy.

Impact of a real-time peer review audit on patient management in a radiation oncology department.

17beta-hydroxysteroid dehydrogenases: physiological roles in health and disease.

CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families.

A germline mutation in KIT in familial diffuse cutaneous mastocytosis.

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Nicotinamide riboside prevents mitochondrial dysfunction in nemaline myopathy type 6.

Retraction: Aqua-soluble DDQ reduces the levels of Dr1 and Ab and inhibits abnormal interactions between Ab and Dr1 and protects Alzheimer's disease neurons from Ab- and Dr1-induced mitochondrial and synaptic toxicities.

Retraction: Breast cancer cell-derived exosome-delivered microRNA-155 targets UBQLN1 in adipocytes and facilitates cancer cachexia-related fat loss.

Editor's Note: Protective effects of antidepressant citalopram against abnormal APP processing and amyloid beta-induced mitochondrial dynamics, biogenesis, mitophagy and synaptic toxicities in Alzheimer's disease.