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Research 91–120 of 1000+
- Disease causing homozygous variants in the human hairless gene
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- Marie-unna hereditary hypotrichosis
- Monilethrix
- Congenital atrichia with papular lesions
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- 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
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Monilethrix: Beaded hair and hypotrichosis in a child
- 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
- Papular atrichia
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- A review of genetic researches of and rogenic alopecia
- Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- 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
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Genes for intermediate filament proteins and the draft sequence of the human genome