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Research 61–90 of 1000+
- Update on hidradenitis suppurativa: connecting the tracts
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Genetic Control/Involvement in Hair Fiber Traits
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Dermatoscopy of hair shaft disorders
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- A 40-Year-Old Woman of African Descent with the Central Scalp Hair Loss
- Current Genetics in Hair Diseases
- Technological Advances in Anti-hair Loss and Hair Regrowth Cosmeceuticals: Mechanistic Breakthroughs and Industrial Prospects Driven by Multidisciplinary Collaborative Innovation
- Follicular and Scarring Disorders in Skin of Color: Presentation and Management
- The first 20 years of skin of color dermatology: An era of advancements in skin, hair, and nail disorders
- A Holistic Approach to Unravel Keloid Pathogenesis and Optimize Therapeutic Outcomes
- Research progress in the treatment of non-scarring alopecia: mechanism and treatment
- Risk factors and comorbidities associated with central centrifugal cicatricial alopecia