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Research 91–120 of 202
- Progeroide Syndrome
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism
- Mucocutaneous Manifestations of Endocrine Disorders
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Use of Antiandrogens as Therapeutic Agents in COVID-19 Patients
- Männlicher Haarausfall – was uns unsere Gene verraten
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Matricellular Proteins in the Homeostasis, Regeneration, and Aging of Skin
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Harnessing miRNA Milk-Derived Exosomes for Hair Loss Disorders: In Vitro Modulation of WNT Signaling and Dermal Papilla Proliferation
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Androgenetic alopecia
- Evolution of long scalp hair in humans