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Research 151–180 of 1000+
- Integrative study of gene expression and protein complexes
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Analysis of the sheep trichohyalin gene: potential structural and calcium-binding roles of trichohyalin in the hair follicle.
- Peripheral patterns of calcitonin‐gene‐related peptide general somatic sensory innervation: Cutaneous and deep terminations
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Androgens induce sebaceous differentiation in sebocyte cells expressing a stable functional androgen receptor
- The role of <i>Atg5</i> gene in tumorigenesis under autophagy deficiency conditions
- TRPV3 Ion Channel: From Gene to Pharmacology
- 1358 PRC1 fine-tunes gene repression and activation to safeguard skin epithelium development and stem cell specification
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- The function of BST2 in γδ T Cells, CD8 T Cells, and macrophages in alopecia areata pathogenesis 4231
- Photobiomodulation and its influence on the regulation of gene expression in human cells: a narrative literature review
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- 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.
- Effect of a transcriptional inactive or absent vitamin D receptor on beta-cell function and glucose homeostasis in mice
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Lineage‐specific requirements of Alx4 function in craniofacial and hair development
- Identification of a Novel MPL Loss of Function Mutation in a Patient with Cyclic Thrombocytopenia and Characterization of This Syndrome
- Expression and Function of FGF5 Isoform in Hair Growth
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform