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Research 961–990 of 1000+
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- The Process of Cornification Evolved From the Initial Keratinization in the Epidermis and Epidermal Derivatives of Vertebrates: A New Synthesis and the Case of Sauropsids
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- The proteomics of keratin proteins
- Targeting integrin pathways: mechanisms and advances in therapy
- Conformational differences in protein disulfide linkages between normal hair and hair from subjects with trichothiodystrophy: A quantitative analysis by Raman microspectroscopy
- Hair growth induction by the tellurium immunomodulator AS101: association with delayed terminal differentiation of follicular keratinocytes and ras‐dependent up‐regulation of KGF expression
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Contrasting Localization of c-Myc with Other Myc Superfamily Transcription Factors in the Human Hair Follicle and During the Hair Growth Cycle
- The role of disulfide bond formation in the structural transition observed in the intermediate filaments of developing hair
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- FOXN1 deficient nude severe combined immunodeficiency
- Finasteride-mediated hair regrowth and reversal of atrophy in a patient with frontal fibrosing alopecia
- Monilethrix Treated with Minoxidil
- Platelet Extracellular Vesicles Loaded Gelatine Hydrogels for Wound Care
- Mapping the accessibility of the disulfide crosslink network in the wool fiber cortex
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- S100A6 Protein—Expression and Function in Norm and Pathology
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Sequence and expression of human hair keratin genes
- SUBEPIDERMAL CALCIFIED NODULE OF THE EAR IN A CHILD WITH HAIR FOLLICLE NEVUS
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Follistatin promotes LIN28B-mediated supporting cell reprogramming and hair cell regeneration in the murine cochlea
- A counter gradient of Activin A and follistatin instructs the timing of hair cell differentiation in the murine cochlea