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Research 841–870 of 1000+
- The resistance mechanisms of bacteria against ciprofloxacin and new approaches for enhancing the efficacy of this antibiotic
- FGF5 is a crucial regulator of hair length in humans
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Tinea genitalis: a new entity of sexually transmitted infection? Case series and review of the literature
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Inflammatory Cytokine TNFα Promotes the Long-Term Expansion of Primary Hepatocytes in 3D Culture
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Expression of Vimentin in hair follicle growth cycle of inner Mongolian Cashmere goats
- Special Biochemical Features of the Hair Follicle
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Mild oxidative stress protects against chemotherapy-induced hair loss
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- A meta-analysis of chemokines in alopecia areata: recruiting immune cells toward the hair follicle
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Insights into male androgenetic alopecia using comparative transcriptome profiling: hypoxia-inducible factor-1 and Wnt/β-catenin signalling pathways
- Zebrafish Model of Hereditary Pigmentary Disorders
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Sweat under surveillance: Loss of immune–metabolic loop during aging