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Research 721–750 of 799
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- Unravelling the threads of central centrifugal cicatricial alopecia
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- The genetic basis of dermatophytosis skin infection susceptibility
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Matriptase-2, A Novel Suppressor of Hepcidin.
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Androgen biosynthetic pathways in the human prostate
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- The molecular basis of human keratin disorders
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- PROTACs: A novel strategy for cancer drug discovery and development
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Host-Directed FDA-Approved Drugs with Antiviral Activity against SARS-CoV-2 Identified by Hierarchical In Silico/In Vitro Screening Methods
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- FOXN1 deficient nude severe combined immunodeficiency
- SWEET SYNDROME: AN UNUSUAL PRESENTATION OF CHRONIC GRANULOMATOUS DISEASE IN A CHILD
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Betaine supplementation is less effective than methionine restriction in correcting phenotypes of CBS deficient mice
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles