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Research 151–180 of 1000+
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Off-Label Use of Botulinum Toxin in Dermatology—Current State of the Art
- Cantú Syndrome Is Caused by Mutations in ABCC9
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Testicular Steroidogenesis
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Understanding, recognizing, and managing toxicities of targeted anticancer therapies
- Recently Identified Forms of Epidermolysis Bullosa
- The role of WNT10B in physiology and disease: A 10-year update
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation
- Hair & Cutaneous Development
- Significance of stress keratin expression in normal and diseased epithelia
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Hair loss and its management in children
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Dermoscopy Research—An Update
- Unruly hair
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome