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Research 661–690 of 1000+
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- Current Genetics in Hair Diseases
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Comparative Effect of Conventional and Non-Conventional Over-the-Counter Treatments for Male Androgenetic Alopecia: A Network Meta-Analysis Study
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Effect of inhibiting prolactin secretion on secondary hair follicle development in cashmere goats
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Comprehensive transcriptome profiling between balding and non-balding scalp of female pattern hair loss in Asian
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis
- Microarray Gene Expression Analysis of Lesional Skin in Canine Pemphigus Foliaceus
- The role of the skin microbiome in wound healing
- Identification of immune microenvironment changes, immune-related pathways and genes in male androgenetic alopecia
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Policistisko olnīcu sindroms pusaudzēm – starppaaudžu, ģenētiskie, dzīves kvalitātes un negausīgas ēšanas aspekti. Promocijas darbs
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Inherited Epidermolysis Bullosa: A Clinical Case
- Two females with hair loss
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- 250 Sweat glands shrink upward with aging, causing dermal layer defects that lead to loss of skin elasticity and wrinkling-establishment of 3D imaging method for skin appendages
- Clinical Snippets
- Unravelling the link between insulin resistance and androgen excess
- Multi-target evaluation of Korean herbal compounds against the SRD5A2 / AR / beta-catenin axis for androgenetic alopecia: Boltz-2 cofold, ChEMBL-anchored ranking, ADMET-AI 107-endpoint safety panel, and pilosebaceous single-cell atlas-constrained prioritization of Saponin Re, Emodin, and Biochanin A