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Research 151–180 of 1000+
- Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- Clonal multipotency and effect of long-term in vitro expansion on differentiation potential of human hair follicle derived mesenchymal stem cells
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Skin signs of systemic diseases
- Keratin disorders: from gene to therapy
- Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation
- Menopause - Andropause - Anti-Aging 2008, 11.-13. Dezember 2008, Wien - Abstracts
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Outcome and clinical–biological characteristics of patients with advanced breast cancer undergoing removal of ovarian/pelvic metastases
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Oral Manifestations of Hematologic and Nutritional Diseases
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome
- Genetics of Structural Hair Disorders
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients