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Research 661–690 of 1000+
- Multi-Walled Carbon Nanotubes can Promote Root Hair Development Through Nitric Oxide and Ethylene Pathways
- cis-Element- and Transcriptome-Based Screening of Root Hair-Specific Genes and Their Functional Characterization in Arabidopsis
- Histological and dermatoscopic description of sphynx cat skin
- Pathological Studies of Cross‐Related Congenital Hypotrichosis in Cattle
- Interaction of the vacuolar H+-pyrophosphatase AVP1 with the secondary transporters AtNHX1 and SOS1 in Arabidopsis thaliana: Implications in salt tolerance and mineral nutrition
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Hair follicle morphogenesis and epidermal homeostasis in we/we wal/wal mice with postnatal alopecia
- Abstract 4385: Live-imaging the interface between homeostasis and cancer initiation
- The transcriptional repressor CDP (Cutl1) is essential for epithelial cell differentiation of the lung and the hair follicle
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Auxin Input Pathway Disruptions Are Mitigated by Changes in Auxin Biosynthetic Gene Expression in Arabidopsis
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Wool fiber curvature is correlated with abundance of K38 and specific keratin‐associated proteins
- 361 p120-catenin regulates epidermal inflammation in a cadherin-dependent manner
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- The Function of LPR1 is Controlled by an Element in the Promoter and is Independent of SUMO E3 Ligase SIZ1 in Response to Low Pi Stress in Arabidopsis thaliana
- The Effect of Copper Supplementation on the Brindled Mouse
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- Characterization of an autoimmune condition associated with AEC syndrome
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice