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Research 31–60 of 1000+
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Congenital hair loss disorders: Rare, but not too rare
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets.
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- p63 regulates <i>Satb1</i> to control tissue-specific chromatin remodeling during development of the epidermis
- Obesity and the skin
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Quoi de neuf en recherche dermatologique ?
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study