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Research 211–240 of 601
- Genetic Defects of Female Sexual Differentiation
- PRP for skin rejuvenation
- From Old to New: Trends in Drug Repurposing for Modern Medicine
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Regulatory T cells in dominant immunologic tolerance
- Selective Expansion of Tregs Using the IL-2 Cytokine Antibody Complex Does Not Reverse Established Alopecia Areata in C3H/HeJ Mice
- ANAPLASMOSIS IN KINTAMANI CROSSBREED DOG: A CASE REPORT
- Targeted photochemotherapy in alopecia areata
- Repurposed Drugs: Current Trends in Drug Discovery
- Tinea Kapitis pada Dua Saudara Kandung
- Low-level laser treatment promotes skin wound healing by activating hair follicle stem cells in female mice
- Hair follicle epithelial stem cells contribute to interfollicular epidermis during homeostasis
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Hairy tale of signaling in hair follicle development and cycling
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Advancements and challenges in stem cell transplantation for regenerative medicine
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- Immunohistochemical analysis of procathepsin L and cathepsin B in cutaneous Kaposi's sarcoma
- Targeting cardiac hypertrophy through a nuclear co‐repressor
- Generation of iPS-derived model cells for analyses of hair shaft differentiation
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome