Search
for
Sort by
Research 121–150 of 1000+
- Identifying causal genes in alopecia areata using integrative analysis of differential expression and Mendelian randomization
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Cloning, computational analysis and expression profiling of steroid 5 alpha-reductase 1 (SRD5A1) gene during reproductive phases and ovatide stimulation in endangered catfish, Clarias magur
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Melatonin promotes Cashmere goat (<i>Capra hircus</i>) secondary hair follicle growth: a view from integrated analysis of long non-coding and coding RNAs
- Different gene expression profile observed in dermal papilla cells related to androgenic alopecia by DNA macroarray analysis
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Prediction of male-pattern baldness from genotypes
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Genetic Fate Mapping Using Site-Specific Recombinases
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Bioinformatics analysis and verification of m6A related genes based on the construction of keloid diagnostic model