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Research 601–630 of 815
- Localized alopecia and suppression of hypothalamic-pituitary-adrenal (HPA) axis in dogs following treatment with difluprednate 0.05% ophthalmic emulsion (Durezol®)
- Skin epidermal keratinocyte p53 induces food uptake upon UV exposure
- Integrative Analysis of the Metabolome and Transcriptome Reveals the Mechanism Underlying Differences in Skin Development Between the New Zealand Rabbit and the Rex Rabbit
- XIAP Stabilizes DDRGK1 to Promote ER‐Phagy and Protects Against Noise‐Induced Hearing Loss
- SRD5A2 and emerging therapies in androgen-driven disorders
- An <i>mTurq2-Col4a1</i> mouse model allows for live visualization of mammalian basement membrane development
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- Hair & Cutaneous Development
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
- Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- SAT-288 Successful Virilization of a PAIS Patient with a Missense Mutation In The Ligand-binding Domain Of The Androgen Receptor with Combined High-dose Testosterone and Aromatase Inhibitor
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- The long and the short of it: evidence that <i>FGF5</i> is a major determinant of canine ‘hair’‐itability
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Association analysis of polymorphisms in six keratin genes with wool traits in sheep
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family