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Research 331–360 of 889
- Unique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratins
- Pooled safety and tolerability data from four placebo-controlled teriflunomide studies and extensions
- 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
- Teriflunomide in multiple sclerosis: an update
- 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.
- Biochemical changes and liver tissue pathology in weanling Wistar albino rats with protein-energy malnutrition (PEM).
- Nonalcoholic fatty liver disease in young adult Egyptian women with polycystic ovary syndrome
- 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
- A population pharmacokinetic model for individualized regimens of finasteride according to CYP3A5 genotype and liver function
- Ingestion of minoxidil associated with elevated transaminases in the absence of ischemic hepatitis
- Effects of Abuse of Anabolic Androgenic Steroids on Iraqi Athletes
- Drugs affecting blood coagulation, fibrinolysis, and hemostasis
- Diabetex: A novel approach for diabetic wound healing
- Hyperadrenocorticism Associated with Sex Steroid Excess
- 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
- Metabolic Engineering of Microorganisms to Produce L-Aspartate and Its Derivatives
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- 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