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Research 961–990 of 1000+
- Selective Expansion of Tregs Using the IL-2 Cytokine Antibody Complex Does Not Reverse Established Alopecia Areata in C3H/HeJ Mice
- miR-129-5p Participates in Hair Follicle Growth by Targeting HOXC13 in Rabbit
- Caffeine Induces Autophagy and Apoptosis in Auditory Hair Cells via the SGK1/HIF-1α Pathway
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- What does the research say about androgen use and cerebrovascular events?
- Dermal lymphatic dilation in a mouse model of alopecia areata
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Evo Devo of the Vertebrates Integument
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- lncRNA2919 Suppresses Rabbit Dermal Papilla Cell Proliferation via trans-Regulatory Actions
- Cellular Senescence and Aging in Myotonic Dystrophy
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Transcription Factor DLX5 Promotes Hair Follicle Stem Cell Differentiation by Regulating the c-MYC/microRNA-29c-3p/NSD1 Axis
- TMT-Based Quantitative Proteomic Analysis Reveals the Effect of Bone Marrow Derived Mesenchymal Stem Cell on Hair Follicle Regeneration
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- “Structural imprinting” of the cutaneous immune effector function
- Pigmented Epithelioid Melanocytoma (PEM)/Animal Type Melanoma (ATM): Quest for an Origin. Report of One Unusual Case Indicating Follicular Origin and Another Arising in an Intradermal Nevus
- Types of Human Stem Cells and Their Therapeutic Applications
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Molecular Evolution and Protein Structure Variation of Dkk Family
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- MG53 Mitigates Nitrogen Mustard-Induced Skin Injury
- Pharmacological Activity of Cepharanthine
- Application of stem cells in regeneration medicine
- Discovery and Functional Analysis of Secondary Hair Follicle miRNAs during Annual Cashmere Growth