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- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- 666 Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in follicular dystrophy and primary cicatricial alopecia
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Effects of cyclosporine A on clinical and histologic abnormalities in dogs with sebaceous adenitis
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Acne
- Loss of ERBB2 and ERBB3 Receptors Impacts Epidermal Differentiation in Mice
- Cutaneous Tumours of Pilar Origin with Associated Syndromes
- Loss of epidermal PLCg1 induced sebaceous gland hyperplasia and sparse hair
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- Development and homeostasis of the sebaceous gland
- Growth of the Mouse Coat VII. Hair Cycles and Sebaceous Glands in Homozygous and Heterozygous Naked Mice
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling
- Male Pattern Alopecia A Histopathologic and Histochemical Study
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- Smad7-Induced β-Catenin Degradation Alters Epidermal Appendage Development
- Mitochondrial Function in Murine Skin Epithelium Is Crucial for Hair Follicle Morphogenesis and Epithelial–Mesenchymal Interactions
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression