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Research 451–480 of 1000+
- Wnt target gene Ascl4 is dispensable for skin appendage development
- Occipital donor area grading and profile in Indian population
- Natural ‘Green’ Sugar-Based Treatment for Hair Styling
- Combination therapy of orally administered glycyrrhizin and UVB improved active-stage generalized vitiligo
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Acidic and basic hair/nail ("hard") keratins: their colocalization in upper cortical and cuticle cells of the human hair follicle and their relationship to "soft" keratins.
- Defective trophoblast function in mice with a targeted mutation of Ets2
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Mouse notch: expression in hair follicles correlates with cell fate determination.
- Hair follicle-specific keratins and their diseases
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- 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
- 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
- Sequence and Expression of Murine Type I Hair Keratins mHa2 and mHa3
- Contrasting Localization of c-Myc with Other Myc Superfamily Transcription Factors in the Human Hair Follicle and During the Hair Growth Cycle
- 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
- FOXN1 deficient nude severe combined immunodeficiency
- The Proteins of Normal and Aberrant Hair Keratins
- 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