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Research 31–60 of 1000+
- 223 Canonical and Dominant Negative Peroxisome Proliferator-Activated Receptor γ Isoforms are Differentially Expressed in Human Skin and Skin Appendages
- 1381 Molecular mechanisms of donor dominance in androgenetic alopecia
- 863 Molecular basis of hair follicle donor dominance in androgenetic alopecia and sexual dimorphism of the skin
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation
- Interventions for preventing the progression of autosomal dominant polycystic kidney disease
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- A BIOCHEMICAL MARKER IN A DOMINANT MOUSE TRAIT
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Chronic Pelvic Neuralgia Following Finasteride Exposure: A Case Report Suggestive of Nociplastic Dominant Pain
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- An intergenerational androgenic mechanism of female intrasexual competition in the cooperatively breeding meerkat
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Association of Rs231775 Genetic Variant of Cytotoxic T-lymphocyte Associated Protein 4 with Alopecia Areata Disease in Males: A Case–Control Study
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Precocious puberty in a 24 month old Nigerian girl: case report
- 078 The transmembrane protein LRIG1 regulates receptor tyrosine kinases in skin development and homeostasis
- Clinical Snippets
- Does the Recipient Site Influence the Hair Growth Characteristics in Hair Transplantation?
- Hair transplantation surgery