Search
for
Sort by
Research 781–810 of 1000+
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Sulfotransferases, sulfatases and formylglycine-generating enzymes: a sulfation fascination
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Next generation human skin constructs as advanced tools for drug development
- Ectopic Expression of the nude Gene Induces Hyperproliferation and Defects in Differentiation: Implications for the Self-Renewal of Cutaneous Epithelia
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Evidence That the Satin Hair Mutant Gene Foxq1 Is among Multiple and Functionally Diverse Regulatory Targets for Hoxc13 during Hair Follicle Differentiation
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- The genetics of hair shaft disorders
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Clock genes, hair growth and aging
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Decreased Androgen Receptor Gene Methylation in Premature Pubarche: A Novel Pathogenetic Mechanism?
- Concerted gene duplications in the two keratin gene families
- Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- Molecular Genetic and Endocrine Mechanisms of Hair Growth
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Primary Generalized Glucocorticoid Resistance and Hypersensitivity
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family