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Research 211–240 of 1000+
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- A Role for Steroid 5 alpha-reductase 1 in Vascular Remodelling During Endometrial Decidualisation
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- 公表学術論文等リスト 2018
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Physiological and retinoid-induced proliferations of epidermis basal keratinocytes are differently controlled
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- YAP and TAZ are essential for basal and squamous cell carcinoma initiation
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Nonclassic adrenal hyperplasia
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Androgenetic Alopecia: In Vivo Models
- ROR2 regulates self-renewal and maintenance of hair follicle stem cells
- Indian Hedgehog Controls Proliferation and Differentiation in Skin Tumorigenesis and Protects against Malignant Progression