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Publications by Amarilla Mandola
A Novel Homozygous Mutation in CIITA Resulting in MHC Class II Deficiency in an Adult Patient
LymphoSign Journal
Chronic Mucocutaneous Candidiasis Associated With a Novel Frameshift Mutation in IL-17 Receptor Alpha (IL-17RA)
LymphoSign Journal
Related publications
Mice Lacking the MHC Class II Transactivator (CIITA) Show Tissue-Specific Impairment of MHC Class II Expression
Immunity
Infectious Diseases
Allergy
Immunology
Promoter-Specific Functions of CIITA and the MHC Class II Enhanceosome in Transcriptional Activation
EMBO Journal
Immunology
Molecular Biology
Biochemistry
Microbiology
Neuroscience
Medicine
Genetics
MHC Class II Transactivator (CIITA) Expression Is Upregulated in Multiple Myeloma Cells by IFN-γ
Molecular Immunology
Immunology
Molecular Biology
Novel Homozygous GBA2 Mutation in a Patient With Complicated Spastic Paraplegia
Clinical Neurology and Neurosurgery
Medicine
Surgery
Neurology
Revisiting the Specificity of the MHC Class II Transactivator CIITA in Classical Murine Dendritic Cells in Vivo
European Journal of Immunology
Allergy
Immunology
Spontaneous Thrombosis in a Patient With Factor XI Deficiency Homozygous for the p.Cys398Tyr Mutation
Cumhuriyet Medical Journal
Medicine
A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant Without Obvious Maternal Virilisation
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Novel Homozygous Truncating Mutation in LAMB2 Gene in a Chinese Uyghur Patient With Severe Phenotype Pierson Syndrome
Frontiers in Medicine
Medicine
GNE Myopathy in Turkish Sisters With a Novel Homozygous Mutation
Case Reports in Neurological Medicine
