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Research 661–690 of 1000+
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- A counter gradient of Activin A and follistatin instructs the timing of hair cell differentiation in the murine cochlea
- Rapamycin but not acarbose decreases age-related loss of outer hair cells in the mouse Cochlea
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Targeted expression of SV40 T antigen in the hair follicle of transgenic mice produces an aberrant hair phenotype
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Oil body bound oleosin-rhFGF9 fusion protein expressed in safflower (Carthamus tinctorius L.) stimulates hair growth and wound healing in mice
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- SOX9 in organogenesis: shared and unique transcriptional functions
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Evaluation of noninvasive biospecimens for transcriptome studies
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Identification of functional circRNAs regulating ovarian follicle development in goats
- ALKBH5-mediated m6A demethylation fuels cutaneous wound re-epithelialization by enhancing PELI2 mRNA stability
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Androgens in cervical cancer: Their role in epidemiology and biology
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile
- ROBO4 deletion ameliorates PAF-mediated skin inflammation via regulating the mRNA translation efficiency of LPCAT1/LPCAT2 and the expression of PAF receptor