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Research 241–270 of 1000+
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Association Between Natural Hair Color, Race, and Alopecia
- Toward Optimal Health: The Experts Respond to Hair Loss in Women
- Characterizing hair loss in female patients with systemic lupus erythematosus (SLE)
- Hair loss and herbs for treatment
- Miniaturized hairs maintain contact with the arrector pili muscle in alopecia areata but not in androgenetic alopecia: A model for reversible miniaturization and potential for hair regrowth
- Biotinidase deficiency characterized by skin and hair findings
- Hair and scalp disorders
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Hair and scalp disorders in ethnic populations
- The genetic basis of dermatophytosis skin infection susceptibility
- What does acne genetics teach us about disease pathogenesis?
- A review of the treatment of male pattern hair loss
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- The Dickkopf Protein Family in Non-Neoplastic Disorders: Emerging Roles and Therapeutic Targeting
- Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
- A rare hair loss in children: Monilethrix
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Understanding Pattern Hair Loss—Hair Biology Impacted by Genes, Androgens, Prostaglandins and Epigenetic Factors
- The Naked (N) Mutation, Chromosome 15
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients