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Research 541–570 of 895
- Pooled safety and tolerability data from four placebo-controlled teriflunomide studies and extensions
- Clinical and hepatic evaluation in adult dengue patients: a prospective two-month cohort study
- Sequential Morphologic and Clinicopathologic Alterations in Dogs with Experimentally Induced Glucocorticoid Hepatopathy
- High dose interferon treatment in chronic hepatitis C.
- Identification of a preferred substrate peptide for transglutaminase 3 and detection of <i>in situ</i> activity in skin and hair follicles
- Prevalence of nutritional deficiencies in hair loss among Indian participants: Results of a cross-sectional study
- Optimal laboratory testing protocol for patients with acne taking oral isotretinoin
- THE N- AND C-TERMINAL END GROUPS OF HAIR KERATIN
- Hair and amino acids: the interactions and the effects.
- Clinical Manifestations of Dermatomyositis
- Hepatoprotective Activity of Yellow Chinese Chive against Acetaminophen-Induced Acute Liver Injury via Nrf2 Signaling Pathway
- Comprehensive characterization of keratin extracted from patients with androgenetic alopecia and healthy individuals through multimolecular spectroscopy and structural analysis
- Šunų Kraujo Rodiklių ir kliniškai Simptomų pokyčių įvertinimas, esant prieinksčių funkcijų sutrikimams
- Ingestion of minoxidil associated with elevated transaminases in the absence of ischemic hepatitis
- Drugs affecting blood coagulation, fibrinolysis, and hemostasis
- Hyperadrenocorticism Associated with Sex Steroid Excess
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Action of Nucleophilic Reagents on Hair Keratin
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Structural optimization of pep7, a small peptide extracted from epimorphin, for effective induction of hair follicle anagen
- Rand Protease: The Role of Calcium-Binding Site on Stability with Mutagenesis and The Effectiveness on Leather Dehairing
- 1452 Noncoding dsRNA stimulates exosome biosynthesis to regulate skin regeneration
- Etoposide sensitizes CT26 colorectal adenocarcinoma to radiation therapy in BALB/c mice
- 851 The role of astrotactin2 in regulating mammalian skin polarity
- Case Report: Diffuse Hypertrichosis in the Course of Hepatitis C Treatment by IFN-<i>α</i> and Ribavirin
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Design of a RADA16-based self-assembling peptide nanofiber scaffold for biomedical applications