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Research 691–720 of 1000+
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- The developmental basis of fingerprint pattern formation and variation
- Alopecia Universalis Successfully Treated With Adalimumab
- Recent advances on skin‐resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti‐aging and cancer therapies
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- The influence of interferon on healthy and diseased skin
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)
- The Story of the Finest Armor: Developmental Aspects of Reptile Skin
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Engineering molecular imaging strategies for regenerative medicine
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Transcriptomic regulation of seasonal coat color change in hares
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- Skin Development and Disease: A Molecular Perspective
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Association of atopic dermatitis with autoimmune diseases: A bidirectional and multivariable two-sample mendelian randomization study
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Expression analysis of KAP9.2 and Hoxc13 genes during different cashmere growth stages by qRT-PCR method
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- JAK-STAT1 as therapeutic target for EGFR deficiency-associated inflammation and scarring alopecia
- Genetically predicted levels of circulating cytokines and the risk of six immune skin diseases: a two-sample Mendelian randomization study
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains
- A novel eco-friendly Acinetobacter strain A1-4-2 for bioremediation of aquatic pollutants