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Research 601–630 of 675
- 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
- Ubiquity and Diversity of Human-Associated Demodex Mites
- A Dispute Between the Cavendish and Caltech: The Emergence and Ubiquity of the α-Helix
- Molecular elements of the regulatory control of keratin filament modulator AHF/trichohyalin in the hair follicle
- Degradation of human hair keratin scaffold implanted for repairing injured skeletal muscles.
- OsUEV1B, an Ubc enzyme variant protein, is required for phosphate homeostasis in rice
- Degradation of human hair keratin scaffold material used to repair injured skeletal muscles of rabbits
- Comparative ubiquitinomics of human skin reveals insulin receptor ubiquitination as a regulator of collagen secretion
- Clinical Translation of Targeted Protein Degraders
- De Novo-Designed Bifunctional Proteins for Targeted Protein Degradation
- PROTACs in cancer therapy: targeted degradation of GPX4, PARP and epigenetic regulators
- A CLINICAL STUDY OF GERIATRIC DERMATOSES
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Androgens in women
- Does tachyphylaxis occur in long‐term management of scalp seborrheic dermatitis with pyrithione zinc‐based treatments?
- Patterns of keratinocyte carcinoma incidence on the scalp and forehead of non-alopecic women: a retrospective review
- Male pattern hair loss: Taking one for the team: The selfless gene
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- A novel purification procedure for keratin-associated proteins and keratin from human hair
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- New 5?-reductase inhibitors: In vitro and in vivo effects
- Hair keratin film as a substitute device for human hair
- Function and interactions of the Ysc84/SH3yl1 family of actin- and lipid-binding proteins
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Inherited Epidermolysis Bullosa: A Clinical Case
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- Doing Well by Doing Good: The Benevolent Halo of Corporate Social Responsibility
- Interferon alfa-2a in the treatment of cutaneous T cell lymphoma
- Effect of decellularisation methods on methacryloyl-substituted placental ECM hydrogels