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- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Melatonin membrane receptors in peripheral tissues: Distribution and functions
- COVID-19 and endocrine and metabolic diseases. An updated statement from the European Society of Endocrinology
- Nonclassic congenital adrenal hyperplasia
- Farmácia Militar do Laboratório Nacional do Medicamento, Porto e Serviços Farmacêuticos do Centro Hospitalar Universitário do Porto (Hospital de Santo António), EPE, Porto
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Androgen Receptor–Mediated Paracrine Signaling Induces Regression of Blood Vessels in the Dermal Papilla in Androgenetic Alopecia
- Induced Pluripotent Stem Cell Approach to Hair Follicle Regeneration
- CD80 on skin stem cells promotes local expansion of regulatory T cells upon injury to orchestrate repair within an inflammatory environment
- COVID-19 and hypopituitarism
- Expansion Culture of Hair Follicle Stem Cells through Uniform Aggregation in Microwell Array Devices
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- miR-3606-3p alleviates skin fibrosis by integratively suppressing the integrin/FAK, p-AKT/p-ERK, and TGF-β signaling cascades
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- P‐30 Use of fipronil for treatment of <i>Lynxacarus radovskyi</i> in outdoor cats in Rio de Janeiro (Brazil)
- P‐81 A retrospective study of equine sarcoidosis
- Fetal wound healing using a genetically modified murine model: the contribution of P-selectin
- Accumulations of Ca/P in the core of hairs from Taklamakan desert mummies
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Regulation of immune response genes in the skin of allergic and clinically tolerant individuals exposed to p‐phenylenediamine
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- P latelet rich plasma application by dermapen microneedling and intradermal point‐by‐point injection methods, and their comparison with clinical findings and trichoscan in patients with androgenetic alopecia
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- P‐79 Hair follicle growth arrest in Austrian Icelandic horses
- P‐46 A placebo‐controlled, double‐blinded study of recombinant IFNγ in dogs with atopic dermatitis
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog