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- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Genetic mapping of hair loss through the APCDD1 gene pathway: A new perspective
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Identification of novel hair‐growth inducers by means of connectivity mapping
- Mapping Human Skin: One Sequenced Cell at a Time
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Faculty Opinions recommendation of Identification of novel hair-growth inducers by means of connectivity mapping.
- The keratin proteins and genes of wool and hair.
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Alopecia in children
- Inherited Epidermolysis Bullosa: A Clinical Case
- Itpr3 Is Responsible for the Mouse Tufted (tf) Locus
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- 332 Generation of a gene expression signature for sebaceous glands by transcriptome comparison of psoriasis and sebaceous hyperplasia
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Human Trichohyalin Gene Is Clustered with the Genes for Other Epidermal Structural Proteins and Calcium-Binding Proteins at Chromosomal Locus 1q21
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese