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Research 241–270 of 1000+
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- The clock within
- Runx1 transcription factor is involved in the regulation of KAP5 gene expression in human hair follicles
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Staphylococcus aureus accessory gene regulator quorum-sensing system inhibits keratinocyte lipid enzymes and delays wound repair
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Woolly Antics between the Sheaths
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Inherited Epidermolysis Bullosa: A Clinical Case
- 1377 Decoding frontal fibrosing alopecia and lichen planopilaris: Macrophages hold the key?
- Australasian Society for Dermatology Research Meeting, May 2006
- Main Plenary Sessions: Summaries of Papers
- British Society for Dermatopathology: Summaries of Papers
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Alopecia Areata
- Dermatopathology and molecular genetics
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Evidence That the Satin Hair Mutant Gene Foxq1 Is among Multiple and Functionally Diverse Regulatory Targets for Hoxc13 during Hair Follicle Differentiation
- Concerted gene duplications in the two keratin gene families
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia