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Research 511–540 of 1000+
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Androgen Receptor (<i>AR</i>) Gene (CAG)n and (GGN)n Length Polymorphisms and Symptoms in Young Males With Long-Lasting Adverse Effects After Finasteride Use Against Androgenic Alopecia
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Game Changers: Blockbuster Small-Molecule Drugs Approved by the FDA in 2024
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Alopecia: Association with Resistance to Thyroid Hormones
- Disease causing homozygous variants in the human hairless gene
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Hyperadrenocorticism in Ferrets
- Cellular Senescence and Aging in Myotonic Dystrophy
- Spatiotemporal Labeling of Melanocytes in Mice
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- The urine as a diagnostic key for a homozygous EGFR mutation
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Adult Male Hypogonadism: A Laboratory Medicine Perspective on Its Diagnosis and Management
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case