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Research 181–210 of 1000+
- 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
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- 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.
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- 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
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Toxicological Studies on Procyanidin B-2 for Extern?al Application as a Hair Growing Agent
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Validation of Replacement of the Synthetic Food Dye 'Sunset Yellow'-Induced Hepatotoxicity and Genotoxicity with the Nutraceutical 'Curcumin' in Mice