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Research 391–420 of 1000+
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- SOX9 in organogenesis: shared and unique transcriptional functions
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Roles of GasderminA3 in Catagen–Telogen Transition During Hair Cycling
- Animal models and culture methods in the study of hair growth
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- In the quest to stymie time, will laboratory data stand up in man?
- Do Changes in Chromosomes Cause Aging?
- Converging physiological roles of the anthrax toxin receptors
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- The Roles of EDA2R in Ageing and Disease
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Genetics of Inherited Ichthyoses and Related Diseases
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Disorders of Keratinization
- Absence of vitamin D receptor (VDR)‐mediated PPARγ suppression causes alopecia in VDR‐null mice
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Human Regulatory T Cells: Understanding the Role of Tregs in Select Autoimmune Skin Diseases and Post-Transplant Nonmelanoma Skin Cancers
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Dermatologic manifestations of thyroid disease: a literature review
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin