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Research 181–210 of 1000+
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- Disorders of ovulation
- 1123 COPPER LOADING (CuL) STUDIES IN BRINDLED (Br) MOUSE HEMIZYGOTES AND HETEROZYGOTES
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- The genetic basis of dermatophytosis skin infection susceptibility
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- More than one way to skin . . .
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Plain language summaries
- Pleiotropic effects of the nude mutation.
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Cysteine and Glutamine level in hair shaft fractures patients
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Steroid 17β-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Neonatal Occipito-Lınear and Temporo-Fronto-Parıetal Alopecıa: Can Non-Marginal and Marginal forms of the Transient Neonatal Hair Loss be Found Together?
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Congenital hypotrichosis due to short anagen
- The vitamin D receptor, the skin and stem cells