Search
for
Sort by
Research 811–840 of 1000+
- Lipoatrophy and severe metabolic disturbance in mice with fat-specific deletion of PPARγ
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- SEXUAL DIMORPHISM IN MAMMALS
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Regulatory T Cells: the Many Faces of Foxp3
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Combined C3b and Factor B Autoantibodies and MPGN Type II
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Generalized atrophic benign epidermolysis bullosa.
- Clinical application of 5α-reductase inhibitors
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- The nude gene and the skin
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Human Follicular Papilla Cells Carry Out Nonadipose Tissue Production of Leptin
- FOXN1 deficient nude severe combined immunodeficiency
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Cellular heterogeneity and microenvironmental control of skin cancer
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia