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Research 271–300 of 1000+
- The Role of Cell Polarity Regulator aPKC in Hair Follicle Stem Cell Maintenance and Wound Healing
- Cells to Surgery Quiz: April 2020
- Clinical Snippets
- Investigation of Paraoxanase Enzyme Polymorphism in Patients with Alopecia Areata
- Polycystic ovary syndrome
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Allelic frequencies for the seventeen Y-STR loci observed in Iraqi male patients with prostate cancer
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Fertility and Sterility Vol 101 No 4, April 2014
- Evaluation of the relationship between androgenetic alopecia and blood groups and Rhesus factor
- Male pattern hair loss: Taking one for the team: The selfless gene
- Emerging interactions between skin stem cells and their niches
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Association between TLR1 polymorphisms and alopecia areata
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- A meta-analysis of the relationship between vitamin D receptor gene ApaI polymorphisms and polycystic ovary syndrome
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Familial patterns of alopecia areata: A systematic review and meta-analysis
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Chemically induced skin tumors arise from long-lived stem cells of the upper hair follicle
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Localized variant of junctional epidermolysis bullosa with R795X mutation
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- INNOVATIVE APPROACH TO CRC PREVENTION: THE ROLE OF LOW-PENETRATION GENES
- [Usefulness and limitations of the evaluation of sex-hormone-binding globulin in women with a female pattern of androgen-induced baldness].
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa