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Research 541–570 of 1000+
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Splitting Hairs
- Fibroblast growth factors: key players in regeneration and tissue repair
- WNT Signaling in Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- FGF5 is a crucial regulator of hair length in humans
- Epidermal stem cells in wound healing and their clinical applications
- Gene expression profiling of intestinal regeneration in the sea cucumber
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Hox in hair growth and development
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- Bone morphogenetic protein signaling regulates the size of hair follicles and modulates the expression of cell cycle-associated genes
- Keratins and disease at a glance
- A Review of the Use of Biotin for Hair Loss
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- The biology and genetics of curly hair
- Noggin overexpression inhibits eyelid opening by altering epidermal apoptosis and differentiation
- Receptor activator of NF-κB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unit
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Animal and in vitro Models for the Study of Hair Follicles
- Heparan Sulfate Regulates Hair Follicle and Sebaceous Gland Morphogenesis and Homeostasis
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Control by a hair’s breadth: the role of microRNAs in the skin
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations