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Research 481–510 of 1000+
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Off-label uses of retinoids in dermatology
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Role of Phenylalanine and Its Metabolites in Health and Neurological Disorders
- Proceedings of the Ninth World Congress for Hair Research (2015)
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Sex-limited chromosomes and non-reproductive traits
- Toward Elucidating Epigenetic and Metabolic Regulation of Stem Cell Lineage Plasticity in Skin Aging
- Central centrifugal cicatricial alopecia in Black men: A case series highlighting key clinical features in this cohort
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Trailing the Path to Preventive Oncology
- Predicting Physical Appearance from Low Template: State of the Art and Future Perspectives
- Technological Advances in Anti-hair Loss and Hair Regrowth Cosmeceuticals: Mechanistic Breakthroughs and Industrial Prospects Driven by Multidisciplinary Collaborative Innovation
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Autosomal recessive congenital ichthyosis due to <i>PNPLA1</i> mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy