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Research 361–390 of 1000+
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Frontal Fibrosing Alopecia
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Familial congenital generalized hypertrichosis
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- Monilethrix: Beaded hair and hypotrichosis in a child
- Immunolocalization of telomerases in human hairs identifies proliferating cells in the bulb matrix and outer root sheath
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Congenital Atrichia: A Case Report
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Papular atrichia
- Hox demarcates regional regeneration of adult hair follicle stem cells
- A review of genetic researches of and rogenic alopecia
- Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis
- A mouse with bad hair and poor taste
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- Genetics of blond hair
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Screening of Sheep Fibroblast Cell Line with the Spider Dragline Silk Protein Gene
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Letter To Editor-Alopecia universalis in Down syndrome: Response totherapy
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- BRITISH ASSOCIATION OF DERMATOLOGY.
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- Sperm aneuploidy in infertile male patients: a systematic review of the literature