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Research 31–60 of 1000+
- Research landscapes and knowledge structure of cardiac xenotransplantation: A bibliometric analysis
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- 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
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- An analysis of gene expression data involving examination of signaling pathways activation reveals new insights into the mechanism of action of minoxidil topical foam in men with androgenetic alopecia
- Gene Expression Profiling of the Intact Dermal Sheath Cup of Human Hair Follicles
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Genetic Fate Mapping Using Site-Specific Recombinases
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Mapping Metabolism: Monitoring Lactate Dehydrogenase Activity Directly in Tissue
- The clock gene brain and muscle Arnt-like protein-1 (BMAL1) is involved in hair growth
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- JAK-centric explainable few-shot gene-expression diagnosis framework for alopecia via MultiPLIER priors and relation-style set-to-set comparison
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells