Search
for
Did you mean Phenylalanine?
Sort by
Research 30 of 351
- Man made disease: Clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse study
- Raman spectroscopic analysis of L‐phenylalanine and hydrolyzed eggwhite protein penetration into keratin fibers
- Role of Phenylalanine and Its Metabolites in Health and Neurological Disorders
- Synthesis and Biological Evaluation of 4-(4-(Alkyl-and Phenylaminocarbonyl)benzoyl)benzoic Acid Derivatives as Non-steroidal Inhibitors of Steroid 5α-Reductase Isozymes 1 and 2
- Unique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratins
- The long and the short of it: evidence that <i>FGF5</i> is a major determinant of canine ‘hair’‐itability
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- NON-PSORALEN TREATMENT OF VITILIGO. PART II. LESS COMMONLY USED AND EXPERIMENTAL THERAPIES
- Hair Amino Acids: Normal Values and Results in Metabolic Errors
- Cataracts and strabismus associated with hand rearing using artificial milk formulas in Bengal tiger (<i>Panthera tigris spp tigris</i>) cubs
- Hair and amino acids: the interactions and the effects.
- Human hair proteins as natural reactive oxygen species scavengers for in vitro applications
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Evaluation of Resistance Resources and Analysis of Resistance Mechanisms of Maize to Stalk Rot Caused by <i>Fusarium graminearum</i>
- Inhibition of a signaling modality within the gp130 receptor enhances tissue regeneration and mitigates osteoarthritis
- Non-invasive monitoring of low molecular weight biomarkers relevant to skin inflammation and cancer
- Widespread erythematous scaly eruption in an infant with phenylketonuria
- Untargeted metabolomics analysis of plasma metabolic characteristics in patients with acne and insulin resistance
- Phénylcétonurie de l’adulte : manifestations neurologiques et modalités évolutives
- Detection of urine metabolites in polycystic ovary syndrome by UPLC triple-TOF-MS
- Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Analysis of Lower-Limb Ulcers in Participants with Leprosy Sequelae Using Metabolomics and 16S Ribosomal DNA Sequencing
- Biosynthetic studies through feeding experiments in Eclipta prostrata (L.) L. hairy roots
- Uncovering the biosynthetic pathway of bioactive compounds from Eclipta prostrata (L.) L. hairy roots
- Anti-anginal and beta-adrenoceptor blocking drugs
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Optimization of the method for the culture of melanocyte precursors from hair follicles and their activation by 1,25-dihydroxyvitamin D3
- Intractable Diffuse Alopecia Caused by Multifactorial Side-Effects in Treatment of Acute Lymphocytic Leukemia: Connection to Iatrogenic Failure of Estrogen Secretion
- 4-O-Methylhonokiol: A lesser-known neolignan from Magnolia species with diverse and promising pharmacological properties