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Research 931–960 of 1000+
- A patient with Cronkhite-Canada syndrome whose entire digestive tracts was examined endoscopically
- Epithelial Stem Cells: Turning over New Leaves
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- Molecular Mechanisms Responsible for Therapeutic Potential of Mesenchymal Stem Cell-Derived Secretome
- Autoimmunity: Alopecia Areata
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Dermal fibroblast in cutaneous development and healing
- Hair: Its structure and response to cosmetic preparations
- Molecular signaling in feather morphogenesis
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Bone Morphogenetic Protein Signaling Regulates Postnatal Hair Follicle Differentiation and Cycling
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Multi-layered environmental regulation on the homeostasis of stem cells: The saga of hair growth and alopecia
- Platelet-rich plasma as a potential treatment for noncicatricial alopecias
- Choreographing Immunity in the Skin Epithelial Barrier
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Current Advanced Therapies Based on Human Mesenchymal Stem Cells for Skin Diseases
- Controllable Production of Transplantable Adult Human High-Passage Dermal Papilla Spheroids Using 3D Matrigel Culture
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Regionalisation of the skin
- The Genetics of Human Skin Disease
- Dynamic expression of ornithine decarboxylase in hair growth
- Cooperation of TGF‐β and FGF signalling pathways in skin development
- Extracellular vesicles from hair follicle-derived mesenchymal stromal cells: isolation, characterization and therapeutic potential for chronic wound healing