Mutational spectrum of phenylketonuria in Ireland

Pharmacokinetic and pharmacodynamic evaluation of alternative pomalidomide dosing regimens in the treatment of multiple myeloma.

British journal of haematology·2025

Variation in the mu-opioid receptor gene (OPRM1) moderates the influence of maternal sensitivity on child attachment.

Translational psychiatry·2024

Organic osmolytes increase expression of specific tight junction proteins in skin and alter barrier function in keratinocytes.

The British journal of dermatology·2020

CRISPR/Cas9 mediated generation of an ovine model for infantile neuronal ceroid lipofuscinosis (CLN1 disease).

Scientific reports·2019

Dilated cardiomyopathy secondary to vitamin D deficiency and hypocalcaemia in the Irish paediatric population: A case report.

Irish medical journal·2017

Type 1 Tyrosinaemia.

Irish medical journal·2016

Fc-engineering for improved cancer immunotherapy.

Biochemical Society transactions·2026

Where metabolism and virulence meet-sulfoxide reductases as determinants of bacterial survival.

Biochemical Society transactions·2026

Molecular mechanisms of Kir channel gating.

Biochemical Society transactions·2026

Communication is key: combinatorial phosphorylation and functional cross-talk in the RNA polymerase II CTD code.

Biochemical Society transactions·2026

The tumor microenvironment in pancreatic cancer: from composition to therapeutic targeting.

Biochemical Society transactions·2026

Deciphering influenza B virus-derived peptides and their presentation by HLA class I molecules.

Biochemical Society transactions·2026

Narrow Band Imaging Improves Endoscopic Differentiation of Inverted Papillomas From Nasal Polyps.

The Laryngoscope·2026

Epidemiological, Clinical and Viral Genomic Features of Influenza Virus Infections Among Pilgrims During the Grand Magal of Touba Over 7 Years (2018-2024).

Journal of medical virology·2026

Delayed Diagnosis of Common Variable Immunodeficiency Revealed by Recurrent Respiratory Infections and Persistent Mediastinal Lymphadenopathy: A Case Report.

Cureus·2026

Association Between UGT1A9 rs13418420 Polymorphism and Propofol Induction Characteristics in Chinese Female Patients Undergoing Brief Gynecological Procedures.

Pharmacogenomics and personalized medicine·2026

Clinical pearls and pitfalls in inborn errors of immunity: An expert-derived framework for diagnostic pattern recognition.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology·2026

Inebilizumab in AQP4-Seropositive NMOSD: One-Year Follow-Up From a Multicenter, Real-World Study.

Annals of clinical and translational neurology·2026

Related Experiment Videos

Mutational spectrum of phenylketonuria in Ireland

Related Concept Videos

Pharmacokinetic and pharmacodynamic evaluation of alternative pomalidomide dosing regimens in the treatment of multiple myeloma.

Variation in the mu-opioid receptor gene (OPRM1) moderates the influence of maternal sensitivity on child attachment.

Organic osmolytes increase expression of specific tight junction proteins in skin and alter barrier function in keratinocytes.

CRISPR/Cas9 mediated generation of an ovine model for infantile neuronal ceroid lipofuscinosis (CLN1 disease).

Dilated cardiomyopathy secondary to vitamin D deficiency and hypocalcaemia in the Irish paediatric population: A case report.

Type 1 Tyrosinaemia.

Fc-engineering for improved cancer immunotherapy.

Where metabolism and virulence meet-sulfoxide reductases as determinants of bacterial survival.

Molecular mechanisms of Kir channel gating.

Communication is key: combinatorial phosphorylation and functional cross-talk in the RNA polymerase II CTD code.

The tumor microenvironment in pancreatic cancer: from composition to therapeutic targeting.

Deciphering influenza B virus-derived peptides and their presentation by HLA class I molecules.

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Epidemiological, Clinical and Viral Genomic Features of Influenza Virus Infections Among Pilgrims During the Grand Magal of Touba Over 7 Years (2018-2024).

Delayed Diagnosis of Common Variable Immunodeficiency Revealed by Recurrent Respiratory Infections and Persistent Mediastinal Lymphadenopathy: A Case Report.

Association Between UGT1A9 rs13418420 Polymorphism and Propofol Induction Characteristics in Chinese Female Patients Undergoing Brief Gynecological Procedures.

Clinical pearls and pitfalls in inborn errors of immunity: An expert-derived framework for diagnostic pattern recognition.

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Mutational spectrum of phenylketonuria in Ireland

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