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Research 511–540 of 1000+
- Transient mitochondrial DNA double strand breaks in mice cause accelerated aging phenotypes in a ROS-dependent but p53/p21-independent manner
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Stem cells and aberrant signaling of molecular systems in skin aging
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Use of natural molecules as anti-angiogenic inhibitors for vascular endothelial growth factor receptor
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- Ectopic Sebaceous Glands in the Hair Follicle Matrix: Case Reports and Literature Review of this Embryogenic Anomaly
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A review on PCOS: Its causes, symptoms, pathogenesis and management
- Thyroid disorders: An overview of causes and treatment
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Botanical booster: Effective plant molecules for enhancing hair growth
- Managing androgenic alopecia with individualised homeopathic medicine and biochemic remedies- An evidence based single case report
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Morphological, molecular and histopathological identification of Sarcoptes scabieiinfection in a goat herd at Goa, India
- 1351 Investigation of the molecular identity of the junctional zone in human
- Pityriasis rubra pilaris unveiling a case of a new onset hepatitis C infection
- Comorbidities in patients with lichen planopilaris: A retrospective case-control study
- Dapsone Therapy for Pustular Psoriasis: Case Series and Review of the Literature
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Prevalence of Metabolic Syndrome in Patients with Mucosal Lichen Planus: A Case–Control Study
- EFFECT OF PLATELET-RICH PLASMA (PRP) ON HAIRFALL (KHALITYA) ALONG WITH AYURVEDIC MEDICINES- A CASE STUDY
- A ROLE OF JALUAKAAVCHARANAAND NIMBA HARIDRACHOORNA LEPA IN TREATMENT OF INDRALUPTA - A CASE STUDY
- The hair growth promoting effect of Sophora flavescens extract and its molecular regulation
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A Thallium-Based Screening Procedure to Identify Molecules That Modulate the Activity of Ca2+-Activated Monovalent Cation-Selective Channels
- Simulative Evaluation of Taurine Against Alopecia Caused by Stress in Caenorhabditis elegans
- Beyond Circadian Rhythm: Melatonin as a Bio-Regulatory Molecule in Skin and Hair Aesthetics
- Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)