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Research 391–420 of 1000+
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Dermatomyositis Disease in Dogs
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- The Clinical Presentation of Systemic Lupus Erythematosus
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Polycystic ovary syndrome
- Alopecia Areata. Current situation and perspectives
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- British Society for Dermatopathology
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Chronic overlapping pain conditions and nociplastic pain
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle