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Research 331–360 of 1000+
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Differential gene expression profiles in foetal skin of Rex rabbits with different wool density
- The Roles of EDA2R in Ageing and Disease
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Androgenetic Alopecia in Men: An Update On Genetics
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- Modeling animal genomics in mice: An authentic approach for the functional interrogation of evolutionarily and agriculturally critical variants
- From the Microscopic Sweat Gland to Large Datasets: The Power of Quantitative Traits in Dermatology
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- The genetic basis of dermatophytosis skin infection susceptibility
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Spatial transcriptomics of a giant pilomatricoma
- Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Does Androgenic Alopecia Aggravate the Risk of Prostate Cancer? Evidence from Mendelian Randomization
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Past, Present and Future Perspectives of Forensic Genetics
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Wound Healing: A Cellular Perspective