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Research 211–240 of 1000+
- Genetic Hair Disorders: A Review
- Akt2 and SGK3 are both determinants of postnatal hair follicle development
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Sustained Postnatal Skin Regeneration Upon Prenatal Application of Functionalized Collagen Scaffolds
- Niche work when you can get it: collagen XVII and the melanocyte stem cell
- Nelfb promotes dermal white adipose tissue formation through RNA Polymerase II mediated adipogenic gene regulation
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Mechanical forces in skin disorders
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- An Update of Congenital Adrenal Hyperplasia
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Acquired Progressive Kinking of Hair
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Caring for women with polycystic ovary syndrome
- Depletion of S100A4+ stromal cells results in abnormal nipple development and nursing failure
- Hair Follicle Stem Cell SLC3A2 Regulates Epithelial Regenerative Properties
- Adrenal causes of endocrine hypertension in childhood or adolescence
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Gelişmekte olan insan fetüslerinin ve yetişkinlerin derisinde EZH2 ekspresyonu: karşılaştırmalı bir çalışma
- Congenital Atrichia: A Case Report
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Congenital adrenal hyperplasia
- Adverse events of the thyroid peroxidase inhibitor methimazole in the treatment of hyperthyroidism: a comprehensive analysis from the first quarter of 2004 to the first quarter of 2025
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE