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Research 991–1000 of 1000+
- Immunoregulatory Effects of Myeloid-Derived Suppressor Cell Exosomes in Mouse Model of Autoimmune Alopecia Areata
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Synaptic processes and immune-related pathways implicated in Tourette syndrome