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Research 391–420 of 1000+
- Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Production of artificial synthetic spidroin gene 4S-transgenic cloned sheep embryos using somatic cell nuclear transfer
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Development and Molecular Characterization of Human Placental Mesenchymal Stem Cells from Human Aborted Fetal Tissue as a Model to Study Mechanism of Spontaneous Abortion
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- RORA Regulates Autophagy in Hair Follicle Stem Cells by Upregulating the Expression Level of the Sqstm1 Gene
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- Developmental changes of skin quality from breast, back, and thigh of Pekin ducks from 1 to 6 weeks of age
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- The nude gene and the skin
- Role of OsPHR2 on phosphorus homoestasis and root hairs development in rice (<i>Oryza sativa</i>L.)
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Analysis of gene expression patterns and levels in maize hybrids and their parents
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- Identification of immune microenvironment changes, immune-related pathways and genes in male androgenetic alopecia
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study
- 604 DNA dioxygenases TET regulate keratin gene expression and enhancer networks within lineage-specific gene loci during epidermal and hair follicle-specific keratinocyte differentiation
- STAT3 Inhibits Cell Proliferation at Least in Part Via Directly Negatively Regulating FST Gene Expression
- Short sequence repeats of the intergenic spacer regions of ribosomal RNA genes in <i>Malassezia globosa</i> and <i>M. restricta</i> colonizing the scalps of male individuals with and without androgenetic alopecia
- Phosphatidylinositol‐specific phospholipase C2 functions in auxin‐modulated root development
- <i>Mrp4</i>, A New Mitogen-Regulated Protein/Proliferin Gene; Unique in this Gene Family for its Expression in the Adult Mouse Tail and Ear<sup>1</sup>
- Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene