Search
for
Sort by
Research 871–900 of 1000+
- Experimental Induction of Alopecia Areata-Like Hair Loss in C3H/HeJ Mice Using Full-Thickness Skin Grafts
- Tregs: Where We Are and What Comes Next?
- Female pattern hair loss
- In vivo function of VDR in gene expression-VDR knock-out mice
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- The interaction of CaM7 and CNGC14 regulates root hair growth in<i>Arabidopsis</i>
- Long COVID: Clinical characteristics, proposed pathogenesis and potential therapeutic targets
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Tight Junction barriers in human hair follicles – role of claudin-1
- Redefining hormone resistance in prostate cancer
- Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Nonclassic congenital adrenal hyperplasia
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Through the lens of hair follicle neogenesis, a new focus on mechanisms of skin regeneration after wounding
- Ovarian SAHA syndrome is associated with a more insulin-resistant profile and represents an independent risk factor for glucose abnormalities in women with polycystic ovary syndrome: A prospective controlled study
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- Expression Profiles of Reproduction- and Thyroid Hormone-Related Transcripts in the Brains of Chemically-Induced Intersex Frogs
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Insertional mutation of the hairless locus on mouse Chromosome 14
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Retinoic Acid and Mouse Skin Morphogenesis. II. Role of Epidermal Competence in Hair Glandular Metaplasia
- Mesothelial Stem Cells and Stromal Vascular Fraction for Skin Rejuvenation
- The hair shaft: normality, abnormality, and genetics
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- Alterations in transcriptome and antioxidant activity of naturally aged mice exposed to selenium-rich rice