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Research 30 of 382
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- Meibomian gland changes in the rhino (hrrhhrrh) mouse.
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Molecular basis of congenital atrichia in humans and mice.
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Differential activity of 2-methylene-19-nor vitamin D analogs on growth factor gene expression in rhino mouse skin and comparison to all-trans retinoic acid
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Disease causing homozygous variants in the human hairless gene
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa