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Research 211–240 of 1000+
- Evaluation of Gene Expression Patterns in Micrografts Demonstrate Induction of Catagen-Like Processes During Storage
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Effect of Adenovirus-Mediated Expression of Sonic Hedgehog Gene on Hair Regrowth in Mice With Chemotherapy-Induced Alopecia
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Fadrozole and finasteride exposures modulate sex steroid- and thyroid hormone-related gene expression in Silurana (Xenopus) tropicalis early larval development
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Development of gene therapy for inner ear disease: Using bilateral vestibular hypofunction as a vehicle for translational research
- Microarray analysis of androgenetic and senescent alopecia: Comparison of gene expression shows two distinct profiles
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Functional analysis of the PIP5K1A gene in Liaoning Cashmere goats: an investigation based on bioinformatics, tissue localization, and biological functions
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- 1358 PRC1 fine-tunes gene repression and activation to safeguard skin epithelium development and stem cell specification
- Investigating RNA-Seq-based differential gene expression during hair follicle development in Angora goat skin
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- The clock gene brain and muscle Arnt-like protein-1 (BMAL1) is involved in hair growth
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals