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Research 901–930 of 1000+
- Tabby pattern genetics – a whole new breed of cat
- Epigenetic regulation of 5α reductase-1 underlies adaptive plasticity of reproductive function and pubertal timing
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Generalised Glucocorticoid Resistance
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- FGF5 is a crucial regulator of hair length in humans
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Prediction of the Development of Depression in Patients with Autoimmune Thyroiditis and Hypothyroidism
- Decoding the role of <i>OsPRX83</i> in enhancing osmotic stress tolerance in rice through ABA-dependent pathways and ROS scavenging
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- BJD Snippet
- A Receptor-Like Kinase Mediates Ammonium Homeostasis and Is Important for the Polar Growth of Root Hairs in<i>Arabidopsis</i>
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- Universal Dermatology: Bridging Gaps in Skin Health
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Proteomics Reveals the Role of PLIN2 in Regulating the Secondary Hair Follicle Cycle in Cashmere Goats
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Diurnal Preference Predicts Phase Differences in Expression of Human Peripheral Circadian Clock Genes
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Thyroxine Differentially Modulates the Peripheral Clock: Lessons from the Human Hair Follicle
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Major Differences in Expression of Inflammatory Pathways in Skin from Different Body Sites of Healthy Individuals
- Cell Membrane-Camouflaged Nanoparticles Mediated Nucleic Acids Delivery
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA