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Research 211–240 of 1000+
- Androgen receptor activation integrates complex transcriptional effects in osteoblasts, involving the growth factors TGF-β and IGF-I, and transcription factor C/EBPδ
- A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA
- Influence of NUDT15 Genotyping on Dose Intensity of Thiopurine Administration and Long-Term Clinical Outcomes (Hospitalization and Surgery)
- Esrp1-Regulated Splicing of Arhgef11 Isoforms Is Required for Epithelial Tight Junction Integrity
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Keratin Gene Expression in Wool Fibre Development
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Keratin 79 is a PPARA target that is highly expressed by liver damage
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Cantú Syndrome Is Caused by Mutations in ABCC9
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Hub biomarkers in ultrasound-guided bladder cancer and osteosarcoma: Myosin light chain kinase and caldesmon
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- P78 Acrodermatitis enteropathica in children: clinical cases
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- E-Poster
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets