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Research 481–510 of 1000+
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- WNT Signaling in Disease
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- A linear and reticulate crusted keratotic papulopustular eruption: a rare presentation of PRIDE (Papulopustules and/or paronychia, Regulatory abnormalities of hair growth, Itching, and Dryness due to Epidermal growth factor receptor inhibitors) complex
- Depletion of <i>Gsdma1/2/3</i> alleviates PMA-induced epidermal hyperplasia by inhibiting the EGFR–Stat3/Akt pathway
- Sorafenib-Associated Facial Acneiform Eruption
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Keratins: the hair shaft's backbone revealed
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Seborrheic keratosis
- Targeted expression of activated erbB-2 to the epidermis of transgenic mice elicits striking developmental abnormalities in the epidermis and hair follicles.
- Clinical and histological recovery of non-thymoma-associated exfoliative dermatitis in a cat treated with ciclosporin A
- The epidermis: rising to the surface
- Ornithine decarboxylase expression in cutaneous papillomas in SENCAR mice is associated with altered expression of keratins 1 and 10.
- Pathophysiological and Pharmaceutical Considerations for Enhancing the Control of Sarcoptes scabiei in Wombats Through Improved Transdermal Drug Delivery
- Follicular cysts and hyperkeratoses in early mycosis fungoides
- Is Wnt5a overexpression sufficient for generating a psoriasis‐like phenotype in transgenic mice?
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Skin iconography analysis of traumatic anserine folliculosis: Skin image feature of TAF
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Netherton Syndrome
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- A case report of verruca vulgaris on basis of alopecia areata successfully treated with diphenylcyclopropenone
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Immune Privilege Collapse and Alopecia Development: Is Stress a Factor
- Adenohypophysitis Associated with Sebaceous Gland Atrophy in a Dog