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Research 451–480 of 1000+
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Second International Symposium—Epigenetic Regulation of Skin Regeneration and Aging: From Chromatin Biology towards the Understanding of Epigenetic Basis of Skin Diseases
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Suicidality Risks Associated with Finasteride, a 5-Alpha Reductase Inhibitor: An Evaluation of Real-World Data from the FDA Adverse Event Reports
- Efectos de la disminución de los depósitos tisulares de hierro sobre los factores de riesgo cardiovascular en pacientes con hiperandrogenismo ovárico funcional
- Significance of stress keratin expression in normal and diseased epithelia
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Endocrine-skin interactions
- Prevalence, Phenotypes, and Comorbidities of Polycystic Ovary Syndrome Among Indian Women
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- A Case of Ovarian Hyperthecosis in a Postmenopausal Woman
- Polycystic Ovary Syndrome: An Updated Overview Foregrounding Impacts of Ethnicities and Geographic Variations
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Application of Acyzol in the Context of Zinc Deficiency and Perspectives
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Hair loss among a group of Egyptian children
- Testosterone therapy in men: Clinical and pharmacological perspectives
- Ethnic Hair Disorders
- RASopathic alopecia: Hair changes associated with vemurafenib therapy
- Dermatopathology Workshop Summary, Berlin 2004