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Research 931–960 of 1000+
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Sex-limited chromosomes and non-reproductive traits
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Effects of anticonvulsant drugs on chromosomes.
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- The role of the androgen receptor gene CAG repeat polymorphism and X-chromosome inactivation pattern in postmenopausal female pattern hair loss
- Human Trichohyalin Gene Is Clustered with the Genes for Other Epidermal Structural Proteins and Calcium-Binding Proteins at Chromosomal Locus 1q21
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- 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
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- SEXUAL DIMORPHISM IN MAMMALS
- Male-pattern baldness susceptibility locus at 20p11
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Toxicological Studies on Procyanidin B-2 for Extern?al Application as a Hair Growing Agent
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Bloom's syndrome–‐a first report from India