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Research 481–510 of 1000+
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Syndromes of Severe Insulin Resistance (SSIRs)
- Molecular pathology of skin adnexal tumours
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Impact of Hormones on Female Sexual Function and Dysfunction
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Molecular Genetics of Human Hair Diseases
- Gerontobiology of the Hair Follicle
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Nail abnormalities in patients with vitiligo
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Hypotrichosis in a child with olmsted syndrome
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Causes and Management of Hypertrichosis
- Ichthyosis with confetti: clinics, molecular genetics and management
- Physiological Insights from the Vitamin D Receptor Knockout Mouse
- Evaluation of the Safety and Effectiveness of Oral Minoxidil in Children: A Systematic Review
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- The prevalence of polycystic ovary syndrome in a community sample of Iranian population: Iranian PCOS prevalence study
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Health-related quality of life and mental state in women with polycystic ovary syndrome and migration or minority background – A cross-sectional study