Search
for
Sort by
Research 931–960 of 1000+
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- The aetiology and pathogenesis of alopecia areata
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Werner's syndrome: incidental finding during pregnancy
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Genetics of infertility and “assisted fertilization” in the Bible: The case of Abraham and his family
- From the Microscopic Sweat Gland to Large Datasets: The Power of Quantitative Traits in Dermatology
- Decision letter: Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- The Shaven (Sha) Mutation, Chromosome 15
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- The Naked (N) Mutation, Chromosome 15
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes