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Publications by Dale Cooper
A Novel Rat Model of Hereditary Hemochromatosis Due to a Mutation in Transferrin Receptor 2
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Related publications
Interaction of the Hereditary Hemochromatosis Protein HFE With Transferrin Receptor 2 Is Required for Transferrin-Induced Hepcidin Expression
Cell Metabolism
Cell Biology
Molecular Biology
Physiology
Hereditary Hemochromatosis
Annual Review of Nutrition
Medicine
Nutrition
Dietetics
Isolated Growth Hormone Deficiency Type 2 Due to a Novel GH1 Mutation: A Case Report
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Recurrent Hyperparathyroidism Due to a Novel CDC73 Splice Mutation
Journal of Bone and Mineral Research
Endocrinology
Orthopedics
Sports Medicine
Metabolism
Diabetes
A Novel Mutation in CELSR1 Is Associated With Hereditary Lymphedema
Vascular Cell
Computer Networks
Developmental Neuroscience
Neurology
Cell Biology
Communications
A Novel Homozygous Mutation in the WNK1/HSN2 Gene Causing Hereditary Sensory Neuropathy Type 2.
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
Mutation Analysis of Four Chinese Families With Pure Hereditary Spastic Paraplegia: Pseudo- X-Linked Dominant Inheritance and Male Lethality Due to a Novel ATL1 Mutation
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
Novel EXT1 Mutation Identified in a Pedigree With Hereditary Multiple Exostoses
Oncology Reports
Medicine
Cancer Research
Oncology
Juvenile Onset Autoinflammatory Disease Due to a Novel Mutation in TNFAIP3 (A20)
Arthritis Research & Therapy
