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- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- 921 Generation of a new rodent model of scleroderma
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- The Shaven (Sha) Mutation, Chromosome 15
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Molecular genetics of androgen insensitivity
- THE PATHOGENESIS OF ALOPECIA AREATA
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles