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- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Polymorphism in the A2M gene associated with high-quality milk in Murrah buffaloes (Bubalus bubalis)
- A mutation in MAP2 is associated with prenatal hair follicle density
- P78 Acrodermatitis enteropathica in children: clinical cases
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Pseudofolliculitis barbae; current treatment options
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- A newborn presenting with congenital blistering
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Expression and Distribution of the Guanine Nucleotide-binding Protein Subunit Alpha-s in Mice Skin Tissues and Its Association with White and Black Coat Colors
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Leveraging Single Nucleotide Polymorphism Profiling for Precision Skin Care: How SNPs Shape Individual Responses in Cosmetic Dermatology
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Diagnostic approach to low‐renin hypertension
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- Topische Immuntherapie mit Diphenylcyclopropenon bei verschiedenen Typen der Alpecia areata: Assoziation zu klinischen Parametern und einem funktionellen Genpolymorphismus des Interleukin-6-Promotors
- Intra-host SARS-CoV-2 single-nucleotide variants emerged during the early stage of COVID-19 pandemic forecast population fixing mutations
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- Clinical Snippets
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy