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Research 211–240 of 1000+
- FOXN1 deficient nude severe combined immunodeficiency
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Integrating whole-genome re-sequencing and transcriptome data to reveal the molecular mechanism of TBX5 gene regulating feathered feet in Guangxi native chickens
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Australasian Society for Dermatology Research Meeting, May 2006
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- Pigmentary mosaicism: An update
- Comprehensive transcriptome profiling between balding and non-balding scalp of female pattern hair loss in Asian
- Cantú Syndrome Is Caused by Mutations in ABCC9
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Melanocytes: The new Black
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- 744 Role of Sdf1-Cxcr4 signaling in mouse appendage regeneration
- Polycystic ovary syndrome
- Toward understanding scarless skin wound healing and pathological scarring
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Congenital hair loss disorders: Rare, but not too rare
- Human skin color: Origin, variation and significance
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- 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
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation