Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Andres Caro
Uroporphyrinogen III Synthase Knock-In Mice Have the Human Congenital Erythropoietic Porphyria Phenotype, Including the Characteristic Light-Induced Cutaneous Lesions
American Journal of Human Genetics
Genetics
Related publications
548 Prenatal Diagnosis of Congenital Erythropoietic Etic Porphyria
Pediatric Research
Child Health
Pediatrics
Perinatology
46. Gene Therapy of Congenital Erythropoietic Porphyria Using Genetically Modified Induced Pluripotent Stem Cells
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
Metabolic Correction of Congenital Erythropoietic Porphyria With iPSCs Free of Reprogramming Factors
American Journal of Human Genetics
Genetics
Structural Diversity in Metal Ion Chelation and the Structure of Uroporphyrinogen III Synthase
Biochemical Society Transactions
Biochemistry
Feline Congenital Erythropoietic Porphyria: Two Homozygous UROS Missense Mutations Cause the Enzyme Deficiency and Porphyrin Accumulation
Molecular Medicine
Molecular Medicine
Genetics
Molecular Biology
A Novel Ataxin-3 Knock-In Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities
Rat Liver Uroporphyrinogen III Synthase Has Similar Properties to the Enzyme fromEuglena Gracilis, Including Absence of a Requirement for a Reversibly Bound Cofactor for Activity
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Family Evaluations in Acute Intermittent Porphyria Using Red Cell Uroporphyrinogen I Synthetase.
Journal of Medical Genetics
Genetics
The Role of Iron in the Pathogenesis of Porphyria Cutanea Tarda. II. Inhibition of Uroporphyrinogen Decarboxylase.
Journal of Clinical Investigation
Medicine
