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Research 871–900 of 1000+
- Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2%
- Five SNP variability in male pattern hair loss patients and healthy individuals from Russia
- Chronic overlapping pain conditions and nociplastic pain
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Distinct stem cells contribute to mammary gland development and maintenance
- Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Identification of genes and proteins associated with anagen wool growth
- Siberian cats help in solving part of the mystery surrounding golden cats
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Mechanism of androgenic alopecia: Addressing speculations through empirical evidences
- Clinical Impact of Molecular Diagnostics in Endocrinology
- The Association Between Polycystic Ovary Syndrome and Its Dermatological Manifestations
- Finding bald spots on chromosome 20p11
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Pathogenesis of androgenetic alopecia
- Phenotype of Normal Hairline Maturation
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Genomic Analysis of Trichotillomania