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Research 211–240 of 280
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice
- Back to the Roots—An Overview of the Chemical Composition and Bioactivity of Selected Root-Essential Oils
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Female pattern alopecia: current perspectives
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Anticancer agents against malaria: time to revisit?
- The role of WNT10B in physiology and disease: A 10-year update
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Genetic Hair Disorders: A Review
- The investigation and management of hirsutism
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Multiomics-empowered Deep Phenotyping of Ulcerative Colitis Identifies Biomarker Signatures Reporting Functional Remission States
- Thymic Mesenchymal Cells Have a Distinct Transcriptomic Profile
- Intralesional Triamcinolone Acetonide Versus Topical Betamethasone Valearate in the Management of Localized Alopecia Areata.
- Turmeric Essential Oil Constituents as Potential Drug Candidates: A Comprehensive Overview of Their Individual Bioactivities
- Building Fucoidan/Agarose-Based Hydrogels as a Platform for the Development of Therapeutic Approaches against Diabetes
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Making the head: Caspases in life and death
- A Survey of Medicinal Plants on Acharya Prafulla Chandra College Campus
- Associations between clinical data, vaccination status, antibody responses, and post-COVID-19 symptoms in Thais infected with SARS-CoV-2 Delta and Omicron variants: a 1-year follow-up study
- Cellular and Molecular Mechanisms of Wound Repair: From Biology to Therapeutic Innovation
- Advances in Nanotechnology Research in Food Production, Nutrition, and Health
- Practices, Efficacy, and Reported Side Effects Associated with Isotretinoin Treatment in Palestine