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Research 871–900 of 1000+
- Molecular Targeted Agents and Biologic Therapies for Non-small Cell Lung Cancer
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Therapeutic Effect of Superficial Scalp Hypothermia on Chemotherapy-Induced Alopecia in Breast Cancer Survivors
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Congenital triangular alopecia: Is it always confined to fronto-temporal region?
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Treatment of Alopecia in Children
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Discreet monilethrix: De novo mutation on the example of polish families
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- 549 Temporary cell cycle arrest in human scalp hair follicles and their epithelial stem cells by ALRN-6924: A novel strategy to selectively protect p53-wildtype cells against paclitaxel-induced alopecia
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Netherton Syndrome – Responding to Oral Retinoids
- MULTIPLE HEMANGIOMAS OF THE TONGUE AND ORAL CAVITY IN A MYOTONIC DYSTROPHY TYPE 1 PATIENT: A CASE REPORT
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Medicinal Plants for Skin Health: A Holistic Review of Botanical Interventions
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Adsorption of Diclofenac and PFBS on a Hair Keratin Dimer
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Hair Anomalies in a 6-Year-Old Girl
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Platelet-Rich Plasma Therapy for Male and Female Pattern Hair Loss
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia