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Aquatic Toxicology, ISSN 0166-445X, 2000, Volume 49, Issue 1, pp. 89 - 100
A multixenobiotic resistance mechanism (MXR) related to the P- glycoprotein multidrug transporter protein (p-gp) has been identified and characterized in... 
hsp70 | MDR | P-Glycoprotein | Induction | Mytiluscalifornianus | Mytilus californianus | AQUATIC ORGANISMS | CELLS | PERMEABILITY | IDENTIFICATION | GALLOPROVINCIALIS | HEAT-SHOCK-PROTEIN | P-glycoprotein | XENOBIOTICS | induction | MARINE & FRESHWATER BIOLOGY | MDR1 GENE | TOXICOLOGY | EXPRESSION | MULTIDRUG-RESISTANCE GENE | hsp70 protein | double prime P glycoprotein
Journal Article
Journal Article
Osteoporosis International, ISSN 0937-941X, 11/2017, Volume 28, Issue 11, pp. 3277 - 3280
Journal Article
Marine Biology, ISSN 0025-3162, 2002, Volume 140, Issue 2, pp. 343 - 353
Mytilus californianus is a filter feeder that removes seaweed particulates, phytoplankton, and their byproducts from the water. The gills of this animal... 
BROWN-ALGAE | TRANSPORT | MULTIDRUG RESISTANCE | MUSSEL | MARINE & FRESHWATER BIOLOGY | INDUCTION | MULTIXENOBIOTIC DEFENSE-MECHANISM | GALLOPROVINCIALIS | CHEMICAL DEFENSES | DEPENDENCE | REVERSAL
Journal Article
Osteoporosis International, ISSN 0937-941X, 1/2017, Volume 28, Issue 1, pp. 347 - 348
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00198-016-3815-0 
Medicine & Public Health | Orthopedics | Endocrinology | Rheumatology | Osteogenesis imperfecta | Children | Creatine | Isoenzymes | Creatine kinase | Osteogenesis
Journal Article
Journal Article
OSTEOPOROSIS INTERNATIONAL, ISSN 0937-941X, 01/2017, Volume 28, Issue 1, pp. 347 - 348
Journal Article
Marine Biology, ISSN 0025-3162, 02/2002, Volume 140, Issue 2, p. 343
  Mytilus califorianus is a filter feeder that removes seaweed particulates, phytoplankton, and their byproducts from the water. The gills of this animal... 
Proteins | Shellfish | Algae
Journal Article
EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN 1018-4813, 07/2019, Volume 27, Issue 7, pp. 1090 - 1100
Osteogenesis imperfecta (OI) is a rare genetic disorder of the connective tissue and 90% of cases are due to dominant mutations in COLIA1 and COLIA2 genes. To... 
DIAGNOSIS | HEART-DISEASE | COLLAGEN | HELICAL DOMAIN | ABNORMALITIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | I PROCOLLAGEN | GENETICS & HEREDITY | MUTATIONS | PREVALENCE | EPIDEMIOLOGY | SEVERITY | Phenotypes | Collagen (type I) | Connective tissue diseases | Serine | Population studies | Nucleotides | Dentinogenesis | Collagen | Osteogenesis imperfecta | Dentinogenesis imperfecta | Mutation | Osteogenesis | Genotypes
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2011, Volume 6, Issue 1, pp. 88 - 88
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2011, Volume 19, Issue 8, pp. 875 - 881
Journal Article