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- Genetic mapping of hair loss through the APCDD1 gene pathway: A new perspective
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Genetic Fate Mapping Using Site-Specific Recombinases
- Genetic fate-mapping reveals surface accumulation but not deep organ invasion of pleural and peritoneal cavity macrophages following injury
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Alopecia in children
- Hair follicle and interfollicular epidermal stem cells make varying contributions to wound regeneration
- The genetics of alopecia areata
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Alopecia Areata: Updates from the Mouse Perspective
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Developmental Mapping of Hair Follicles in the Embryonic Stages of Cashmere Goats Using Proteomic and Metabolomic Construction
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Evaluating HWE and Association in Genome Wide Association Studies: A Unified Procedure
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype