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Research 61–90 of 1000+
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- On the effects of testosterone on brain behavioral functions
- Clinical Impact of Molecular Diagnostics in Endocrinology
- New Frontiers of Non‐Invasive Detection in Scalp and Hair Diseases: A Review of the Application of Novel Detection Techniques
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Role of hair as Evidence in Investigation: A Forensic Approach
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Induction of hair follicle dermal papilla cell properties in human induced pluripotent stem cell-derived multipotent LNGFR(+)THY-1(+) mesenchymal cells
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Optimized Methodology to Produce Platelet-Rich Plasma and Perform Platelet Aggregation in Patients With Coronary Artery Disease
- Role of skin enzymes in metabolism of topical drugs
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- An Uncontrolled Case Series Using a Botanically Derived, β-Cyclodextrin Inclusion Complex in Two Androgenetic Alopecia-Affected Male Subjects
- Organoid‐Guided Precision Medicine: From Bench to Bedside
- Selection signatures for fiber production in commercial species: A review
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Contact sensitization to hair care allergens in scalp seborrheic dermatitis: associations with disease severity and microbiota profiles