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Research 91–120 of 1000+
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Bloom's syndrome–‐a first report from India
- The hair shaft: normality, abnormality, and genetics
- The genetics of androgenetic alopecia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Effects of anticonvulsant drugs on chromosomes.
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- Human Trichohyalin Gene Is Clustered with the Genes for Other Epidermal Structural Proteins and Calcium-Binding Proteins at Chromosomal Locus 1q21
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- The 5α-Recluctase System and Its Inhibitors
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Increased copy number of the TERT and TERC telomerase subunit genes in cancer cells
- Organization and Expression of Hair Follicle Genes.
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Pallister-Killian Syndrome
- New familial association between ocular coloboma and loose anagen syndrome
- Nosocomial Intravascular Catheter Infections with Extended-spectrum Beta-lactamase-producing<i>Escherichia coli</i>in Calves after Strain Introduction from a Commercial Herd
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Acromegaloid Facial Appearance: Case Report and Literature Review