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Research 811–840 of 1000+
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Evaluation of noninvasive biospecimens for transcriptome studies
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Bachmann–Bupp syndrome and treatment
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature
- Uncovering novel biomarkers and drug targets for androgenetic alopecia via metabolite regulation and multi-tissue validation
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Therapies and nanotherapies for cervical cancer (Review)
- Consensus Document on the Clinical Management of Frontal Fibrosing Alopecia: Recommendations From Spanish Working Group on Trichology and Onychology of the AEDV
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Ocular manifestations in a case of Kallmann syndrome – An interesting case report on isolated gonadotropin-releasing hormone deficiency
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Immune therapies for alopecia areata: evidence and new perspectives
- Genetically determined metabolites in allergic conjunctivitis: A Mendelian randomization study
- RETRACTED: Interleukin‐33 links asthma to alopecia areata: Mendelian randomization and mediation analysis
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Aging skin and non-surgical procedures: a basic science overview
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Concurrent autoimmune and endocrine dysregulation in polycystic ovary syndrome