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Publications by Melissa K. Hartley

Recurrent Loss-Of-Function Mutations Reveal Costs to OAS1 Antiviral Activity in Primates

Cell Host and Microbe

Molecular Biology

Cancer Research

English

Patient-Specific Parameters Associated With Traction in Primary and Revision Hip Arthroscopic Surgery

Orthopaedic Journal of Sports Medicine

Sports Medicine

English

Related publications

Loss-Of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy

American Journal of Human Genetics

English

Loss-Of-Function Mutations in Sodium Channel Nav1.7 Cause Anosmia

Multidisciplinary

English

Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American Journal of Human Genetics

English

Escape Mutations in NS4B Render Dengue Virus Insensitive to the Antiviral Activity of the Paracetamol Metabolite AM404

Antimicrobial Agents and Chemotherapy

Infectious Diseases

English

Homozygous Loss-Of-Function Mutations in SLC26A7 Cause Goitrous Congenital Hypothyroidism

Yearbook of Paediatric Endocrinology

English

Effects of MYBPC3 Loss of Function Mutations Preceding Hypertrophic Cardiomyopathy

English

Making Sense of CBP/P300 Loss of Function Mutations in Skin Tumorigenesis

Journal of Pathology

Forensic Medicine

English

BMP4 Loss-Of-Function Mutations in Developmental Eye Disorders Including SHORT Syndrome

English

Loss-Of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome

American Journal of Human Genetics

English