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Research 31–60 of 1000+
- 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
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- 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
- 706 Predictive modeling of patient response to JAK/STAT inhibitors and dynamic patient-matching
- 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
- Amino Acids Oral Treatment for the Amelioration of Skin, Hair, and Nails Conditions: An Open-Label Study
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Action of Nucleophilic Reagents on Hair Keratin
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Botanical extracts
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Aspartame and its effects on health
- Metabolic Engineering of Microorganisms to Produce L-Aspartate and Its Derivatives
- Роль внеклеточных нуклеиновых кислот в процессах регенерации
- 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
- Care for Adolescents With Polycystic Ovary Syndrome: Development and Prescribing Patterns of a Multidisciplinary Clinic
- Structural optimization of pep7, a small peptide extracted from epimorphin, for effective induction of hair follicle anagen
- Practices, Efficacy, and Reported Side Effects Associated with Isotretinoin Treatment in Palestine