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Research 301–330 of 1000+
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Dermatological drugs, topical agents, and cosmetics
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Efficacy and safety of glucocorticoids in the treatment of progressive muscular dystrophy in children: a systematic review and meta-analysis
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- Relation of Selenium, Vitamin E and Other Factors to Muscular Dystrophy in the Rabbit
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A rare case of woolly hair with unusual associations
- Hair Loss as a Side Effect of Lamotrigine Treatment
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Value of dermoscopy for the diagnosis of monilethrix
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Monilethrix – Case report of a rare disease
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Congenital atrichia with papular lesions
- Frontal Fibrosing Alopecia
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice