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Research 31–60 of 1000+
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Crystalline Cataract and Uncombable Hair
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- The Genetics of Human Skin Disease
- Alopecia and hirsutism*
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Dermatomyositis Disease in Dogs
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Baker′s dozen on the scalp: An interesting case of multiple trichilemmal cyst
- Monilethrix in three generations
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Keratosis Follicularis Spinulosa Decalvans
- Clinical Research Progress on Plum-Blossom Needle Combined Therapy for Androgenic Alopecia
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Androgenetic alopecia: pathogenesis and potential for therapy
- Polycystic ovary syndrome and impact on health
- Androgens and hair loss