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Research 481–510 of 1000+
- Industry update: the latest developments in the field of therapeutic delivery, July 2018
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Trichodystrophies: A hair-raising differential diagnosis
- Melanocytes and Vitiligo (and Hair Graying)
- The Role of Histone Demethylases in Disease
- Woolly Antics between the Sheaths
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Lysocellin, a metabolite of the novel drug ‘alopestatin’, induces G1 arrest and prevents cytotoxicity induced by etoposide
- ER-located Ca2+ ATPase ACA2 regulates Ca2+ cytoplasmic pool linked to root hair growth in Arabidopsis thaliana
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Pharmacology of Induced Artificial Platelets in Regenerative Medicine: Beyond Transfusion
- Concomitant acute alopecia and profound bone marrow suppression: An unusual manifestation of azathioprine toxicity
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Paraoxonase Enzyme Activity and Determination of Phenotypic Polymorphism in Patients with Acne Vulgaris
- ラット精巣におけるビタミンD 代謝関連遺伝子の発現解析
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Diagnosis Of Satoyoshi Syndrome Using A Neuroblastoma Cell (SH-SY5Y) Lysate As Substrate For Western Blot
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Human and animal cells under influence of different lighting and stimulus
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- POSTĘP W DIAGNOZIE I LECZENIU STWARDNIENIA ROZSIANEGO
- PŁYNY- NIE ZA DUŻO, NIE ZA MAŁO, LECZ W SAM RAZ
- ONKOLOGIA OKULISTYCZNA WCZORAJ I DZIŚ