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Research 31–60 of 1000+
- Decision letter: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Characterization of an autoimmune condition associated with AEC syndrome
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Inhibition of mitochondrial respiration prevents BRAF-mutant melanoma brain metastasis
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- 177 The Striatin-Interacting Phosphatase And Kinases complex is important for skin epidermal differentiation and barrier formation
- Mutant Cx43 in Skin Differentiation and Disease
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- Disruption of Smad4 in Mouse Epidermis Leads to Depletion of Follicle Stem Cells
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- A BIOCHEMICAL MARKER IN A DOMINANT MOUSE TRAIT
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Abnormalities of Purkinje Cell Arborization in Brindled Mouse Cerebellum
- A doxycycline- and light-inducible Cre recombinase mouse model for optogenetic genome editing
- Functional analysis of collagen XVII in epithelial cancers and a mouse model
- 1229 Melanocyte cell states defined and visualized in developing mouse skin
- The epidermal growth factor receptor decreases Stathmin 1 and triggers catagen entry in the mouse
- The TFIID subunit TAF4 regulates keratinocyte proliferation and has cell-autonomous and non-cell-autonomous tumour suppressor activity in mouse epidermis
- [Genetic dissection of retinoic acid function in epidermis physiology].
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- 1338 Dermal Wnt/β-catenin activation tunably controls hair follicle initiation
- 361 p120-catenin regulates epidermal inflammation in a cadherin-dependent manner