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Research 601–630 of 1000+
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Types of Human Stem Cells and Their Therapeutic Applications
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Testosterone, sex hormone-binding globulin and dehydroepiandrosterone levels and cervical length of Egyptian women with a history of recurrent miscarriages, polycystic ovary syndrome and without the conditions at three stages of pregnancy
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- HHV-6 reactivations in immunocompetent patients with psychiatric disorders: visual hallucinations or possible interactions?
- Signal integrator function of CXXC5 in Cancer
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Detection of the nuclear translocation of androgen receptor using quantitative and automatic cell imaging analysis
- Endocrine intervention for transsexuals
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- 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.
- Androgen Action in the Ovary
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Hair shaft disorders in children – An update
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Role of the SOX family in cancer immune evasion: Emerging player and promising therapeutic opportunities
- Thyroid Hormone Receptor Agonist Promotes Hair Growth in Mice
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Focal Dermal Hypoplasia Associated With Lymphedema: A Case Report From Saudi Arabia
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing