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Research 751–780 of 1000+
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- A Study of the androgen receptor gene polymorphism and the level of expression of the androgen receptor in androgenetic alopecia among Egyptians
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- Study on genetic polymorphisms of androgen receptor gene and 5α-reductase genes of Han men with androgenetic alopecia in the Eastern China
- Genetic Markers of Male and Female Pattern Hair Loss
- A child with generalized hypertrichosis due to secondary topical minoxidil exposure
- Androgenic alopecia in men: the significance of genetic, hormonal and metabolic factors (prospective cohort comparative study)
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Peripheral patterns of calcitonin‐gene‐related peptide general somatic sensory innervation: Cutaneous and deep terminations
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- Molecular epidemiology of hypospadias: Review of genetic and environmental risk factors
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Biology and Genetics of Hair
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Hox genes in development and beyond