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Research 931–960 of 1000+
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Autoimmune associations of alopecia areata in pediatric population - A study in tertiary care centre
- Frontal Fibrosing Alopecia
- Delayed Cutaneous Wound Healing and Aberrant Expression of Hair Follicle Stem Cell Markers in Mice Selectively Lacking Ctip2 in Epidermis
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Mineral Malnutrition Following Bariatric Surgery
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Natural killer cells in atopic and autoimmune diseases of the skin
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Dermatoscopy of hair shaft disorders
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Role of janus kinase inhibitors in the treatment of alopecia areata
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- The developmental basis of fingerprint pattern formation and variation
- Profile of tofacitinib citrate and its potential in the treatment of moderate-to-severe chronic plaque psoriasis
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path?
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Alopecia and Associated Toxic Agents: A Systematic Review
- Pregnancy and Skin
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- <i>Msx2</i> Prevents Stratified Squamous Epithelium Formation in the Enamel Organ
- Evolution of Trichocyte Keratins
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice