Search
for
Sort by
Research 181–210 of 1000+
- Three-Dimensional Analysis of Sex- and Gonadal Status- Dependent Microglial Activation in a Mouse Model of Parkinson’s Disease
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Platelet-Rich Plasma in the Management of Alopecia: A Systematic Review and Meta-Analysis of Clinical Evidence
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- A missense mutation in Lama3 causes androgen alopecia
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Molecular genetics of androgen insensitivity
- Activation of Polyamine Catabolism Profoundly Alters Tissue Polyamine Pools and Affects Hair Growth and Female Fertility in Transgenic Mice Overexpressing Spermidine/SpermineN 1-Acetyltransferase
- <i>PIK3CA</i> gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effect
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Biochemistry of epidermal stem cells
- The Pathogenesis of Alopecia Areata in Rodent Models
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Transient Ca2+ entry by plasmalogen-mediated activation of receptor potential cation channel promotes AMPK activity
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Radiotherapy-Induced Skin Fibrosis: Pathophysiology, Emerging Therapeutics, and the Role of Dermatology
- Langerin+ Dendritic Cells in Cutaneous Fibrosis: The TGF-β1 Signaling Axis
- Linking Morphogen and Chromatin in the Hair Follicle
- Effect of inhibiting prolactin secretion on secondary hair follicle development in cashmere goats
- A Review of Platelet-Rich Plasma: History, Biology, Mechanism of Action, and Classification
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering