refine search
creatine transport 123
 
creatine transporter activity 123
 
Creatine 135
 
creatine biosynthetic process 39
 
Amidinotransferases 25
 
Mentally Disabled Persons 48
 
Guanidinoacetate N-Methyltransferase 25
 
glycine amidinotransferase activity 20
 
Theory of Mind 50
 
Creatinine 41
 
Authors
Locations
Journals
Publication Dates
Find concepts in Knowledge Base
Explore current query
documentsstatisticstop authorclipboard
179 documents found
1: Title: Treatment outcome of creatine transporter deficiency: international retrospective cohort study.
Authors: Bruun, Theodora U J, et.al. .
Journal: Metabolic brain disease (Metab Brain Dis), 2018 .
Snippet: Combined creatine, arginine and glycine therapy might have stopped disease progression in males and improved phenotype in females.
Affiliation: Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada. Division of Clinical and Metabolic Genetics, Department of Paediatrics, University of Toronto, The Hospital for Sick Children, Toronto, ON, Canada. Department of Biochemistry, University of Oxford, Oxford, UK. Pediatrics, Metabolic Unit, Centro Materno Infantil do Norte, Centro Hospitalar do Porto, Porto, Portugal. Service of Human Genetics, CHU Liège, University of Liège, Liège, Belgium. Department of Pediatrics, Division of Human Genetics, The Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA. Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, NC, North, USA. Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia. Metabolic Unit - Child Development Center, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra (CHUC), Coimbra, Portugal. Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Woluwe-Saint-Lambert, Belgium. Department of Metabolic Paediatrics, Royal Hospital for Sick Children, Belfast, UK. Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia. Departments of Paediatrics and Biochemistry, University of Toronto, Toronto, ON, Canada. Center for Human Genetics, Franche-Comté University, Besançon, France. Metabolic Unit, Department of Clinical Chemistry, VU University Medical Center, Amsterdam Neuroscience, Amsterdam, The Netherlands. Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada. saadet.andrews@sickkids.ca. Division of Clinical and Metabolic Genetics, Department of Paediatrics, University of Toronto, The Hospital for Sick Children, Toronto, ON, Canada. saadet.andrews@sickkids.ca. Institute of Medical Sciences, University of Toronto, The Hospital for Sick Children, Toronto, ON, Canada. saadet.andrews@sickkids.ca. .
Related Products: order online
2: Title: Cognitive deficits and increases in creatine precursors in a brain-specific knockout of the creatine transporter gene Slc6a8.
Authors: Udobi, Kenea C, et.al. .
Journal: Genes, brain, and behavior (Genes Brain Behav), 2018 .
Snippet: Creatine transporter (CrT; SLC6A8) deficiency (CTD) is an X-linked disorder characterized by severe cognitive deficits, impairments in language, and an absence of brain creatine (Cr).
Affiliation: Division of Neurology, Cincinnati Children's Research Foundation and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH. Service de Pharmacologie et Immunoanalyse (SPI), CEA, Université Paris Saclay, Gif-sur-Yvette cedex, France. .
Related Products: order online
3: Title: Astrocytic γ-aminobutyric acid (GABA) transporters mediate guanidinoacetate transport in rat brain.
Authors: Tachikawa, Masanori, et.al. .
Journal: Neurochemistry international (Neurochem Int), Vol. 113, 2017 .
Snippet: In contrast, betaine, a substrate of betaine-GABA transporter 1 (BGT1)/Slc6a12, and creatine, a substrate of creatine transporter (CRT)/Slc6a8, had little inhibitory effect.
Affiliation: Division of Membrane Transport and Drug Targeting, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan; Department of Pharmaceutics, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan. Electronic address: tachik-dds@umin.ac.jp. Department of Pharmaceutics, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan. Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan. Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan; Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan. Department of Pharmaceutics, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan. Electronic address: hosoyak@pha.u-toyama.ac.jp. .
Related Products: order online
4: Title: SLC6 Transporter Folding Diseases and Pharmacochaperoning.
Authors: Freissmuth, Michael, et.al. .
Journal: Handbook of experimental pharmacology (Handb Exp Pharmacol), 2017 .
Snippet: Prominent examples include mutations in the transporters for dopamine (DAT, SLC6A3), for creatine (CT1, SLC6A8), and for glycine (GlyT2, SLC6A5), which result in infantile dystonia, mental retardation, and hyperekplexia, respectively.
Affiliation: Institute of Pharmacology and the Gaston H. Glock Research Laboratories for Exploratory Drug Development, Center of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria. michael.freissmuth@meduniwien.ac.at. Institute of Pharmacology and the Gaston H. Glock Research Laboratories for Exploratory Drug Development, Center of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria. .
Related Products: order online
5: Title: Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder.
Authors: Cameron, Jessie M, et.al. .
Journal: International journal of molecular sciences (Int J Mol Sci), Vol. 18 (8), 2017 .
Snippet: Creatine deficiency syndrome (CDS) comprises three separate enzyme deficiencies with overlapping clinical presentations: arginine:glycine amidinotransferase (GATM gene, glycine amidinotransferase), guanidinoacetate methyltransferase (GAMT gene), and creatine transporter deficiency (SLC6A8 gene, solute carrier family 6 member 8).
Affiliation: Genetics and Genome Biology, Peter Gilgan Center for Research and Learning, Toronto, ON M5G 0A4, Canada. jessie.cameron@sickkids.ca. Genetics and Genome Biology, Peter Gilgan Center for Research and Learning, Toronto, ON M5G 0A4, Canada. Valeriy.Levandovskiy@sickkids.ca. Department of Paediatrics, University of Toronto, Toronto, ON M5S 1A1, Canada. wendy.roberts@sickkids.ca. Holland Bloorview Kids Rehabilitation Hospital, 150 Kigour Rd, Toronto, ON M4G 1R8, Canada. wendy.roberts@sickkids.ca. Department of Paediatrics, University of Toronto, Toronto, ON M5S 1A1, Canada. Evdokia.Anagnostou@sickkids.ca. Holland Bloorview Kids Rehabilitation Hospital, 150 Kigour Rd, Toronto, ON M4G 1R8, Canada. Evdokia.Anagnostou@sickkids.ca. Genetics and Genome Biology, Peter Gilgan Center for Research and Learning, Toronto, ON M5G 0A4, Canada. Stephen.Scherer@sickkids.ca. The Centre for Applied Genomics and Genetics and Genome Biology, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada. Stephen.Scherer@sickkids.ca. McLaughlin Centre and Department of Molecular Genetics, 686 Bay Street, 13th Floor, Peter Gilgan Center for Research and Learning, Toronto, ON M5G 0A4, Canada. Stephen.Scherer@sickkids.ca. Department of Paediatrics, University of Toronto, Toronto, ON M5S 1A1, Canada. Alvin.Loh@SurreyPlace.on.ca. Surrey Place Center, 2 Surrey Place, Toronto, ON M5S 2C2, Canada. Alvin.Loh@SurreyPlace.on.ca. Genetics and Genome Biology, Peter Gilgan Center for Research and Learning, Toronto, ON M5G 0A4, Canada. andreas.schulze@sickkids.ca. Department of Paediatrics, University of Toronto, Toronto, ON M5S 1A1, Canada. andreas.schulze@sickkids.ca. Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada. andreas.schulze@sickkids.ca. .
Related Products: order online
6: Title: Inhibition of the high affinity choline transporter enhances hyperalgesia in a rat model of chronic pancreatitis.
Authors: Luo, Dan, et.al. .
Journal: Biochemical and biophysical research communications (Biochem Biophys Res Commun), Vol. 488 (1): 204-210, 2017 .
Snippet: CHT1 expression in pancreas-specific dorsal root ganglia (DRGs) was assessed through immunohistochemistry and western blotting.
Affiliation: Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, China; Key Laboratory of Hubei Province for Digestive System Diseases, Wuhan, China. Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, China; Key Laboratory of Hubei Province for Digestive System Diseases, Wuhan, China. Electronic address: yubaop62@163.com. .
Related Products: order online
7: Title: Creatine biosynthesis and transport by the term human placenta.
Authors: Ellery, Stacey J, et.al. .
Journal: Placenta, Vol. 52, 2017 .
Snippet: qPCR was used to determine the mRNA expression of the creatine synthesising enzymes arginine:glycine amidinotransferase (AGAT) and guanidinoacetate methyltransferase (GAMT), and the creatine transporter (SLC6A8).
Affiliation: The Ritchie Centre, Hudson Institute of Medical Research, Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia. Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Deakin University, Burwood Campus, Melbourne, Australia. Department of Obstetrics and Gynaecology, Monash University & Monash Health, Melbourne, Australia. The Ritchie Centre, Hudson Institute of Medical Research, Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia; Department of Medicine, School of Clinical Sciences, Monash University, Monash Medical Centre, Clayton, Australia. The Ritchie Centre, Hudson Institute of Medical Research, Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia. Electronic address: Hayley.Dickinson@hudson.org.au. .
Related Products: order online
8: Title: Does maternal-fetal transfer of creatine occur in pregnant sheep?
Authors: Baharom, Syed, et.al. .
Journal: American journal of physiology. Endocrinology and metabolism (Am J Physiol Endocrinol Metab), Vol. 313 (1): E75-E83, 2017 .
Snippet: Presence of the creatine transporter-1 (SLC6A8) and l-arginine:glycine amidinotransferase (AGAT; the enzyme synthesizing GAA) proteins were determined by Western blots of placental cotyledons.
Affiliation: The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Australia. Department of Anatomy and Developmental Biology, Monash University, Melbourne, Australia. Faculty of Medicine, Universiti Teknologi MARA, Sungai Buloh, Selangor, Malaysia. Institute for Physical Activity and Nutrition, Deakin University, Melbourne, Australia. Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia; and. Institute for Physical Activity and Nutrition, Deakin University, Melbourne, Australia; rsnow@deakin.edu.au. .
Related Products: order online
9: Title: Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity.
Authors: Heussinger, Nicole, et.al. .
Journal: Pediatric neurology (Pediatr Neurol), Vol. 67, 2017 .
Snippet: BACKGROUND: The X-linked creatine transporter deficiency (CRTD) caused by an SLC6A8 mutation represents the second most common cause of X-linked intellectual disability.
Affiliation: Department of Pediatrics, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany. Electronic address: Nicole.heussinger@klinikum-ab-alz.de. Department of Radiology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany. Department of Neuroradiology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany. Department of Pediatrics, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany. .
Related Products: order online
10: Title: Abnormal N-Glycosylation of a Novel Missense Creatine Transporter Mutant, G561R, Associated with Cerebral Creatine Deficiency Syndromes Alters Transporter Activity and Localization.
Authors: Uemura, Tatsuki, et.al. .
Journal: Biological & pharmaceutical bulletin (Biol Pharm Bull), Vol. 40 (1): 49-55, 2017 .
Snippet: Cerebral creatine deficiency syndromes (CCDSs) are caused by loss-of-function mutations in creatine transporter (CRT, SLC6A8), which transports creatine at the blood-brain barrier and into neurons of the central nervous system (CNS).
Affiliation: Department of Pharmaceutical Microbiology, Graduate School of Pharmaceutical Sciences, Kumamoto University. .
Related Products: order online
11: Title: Down-Regulation of the Na+,Cl- Coupled Creatine Transporter CreaT (SLC6A8) by Glycogen Synthase Kinase GSK3ß.
Authors: Fezai, Myriam, et.al. .
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology (Cell Physiol Biochem), Vol. 40 (5): 1231-1238, 2016 .
Snippet: BACKGROUND: The Na+,Cl- coupled creatine transporter CreaT (SLC6A8) is expressed in a variety of tissues including the brain.
Affiliation: Department of Physiology I, University of Tuebingen, Tuebingen, Germany. .
Related Products: order online
12: Title: Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.
Journal: Molecular neurobiology (Mol Neurobiol), 2016 .
Snippet: Furthermore, we describe the first manifesting carrier female with deletion of SLC6A8 and BCAP31 genes on Xq28.
Affiliation: Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran. Pediatric Neurorehabilitation Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Child and Adolescent Psychiatry Department, Zahedan University of Medical Sciences, Zahedan, Iran. Research Center for Children and Adolescents Health, Zahedan University of Medical Sciences, Zahedan, Iran. Shahroud Welfare Organization, Shahroud, Iran. Health Psychology Department, Edalat University, Tehran, Iran. Genetics of Non-communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran. Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran. Department of Neurology, School of Medicine, Imam Khomeini Hospital and Iranian Center of Neurological Research, Tehran University of Medical Sciences, Tehran, Iran. Bahar Education and Rehabilitation Center for the handicapped, Tehran, Iran. Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. f_behjati@uswr.ac.ir. .
Related Products: order online
13: Title: Creatine transporter deficiency: Novel mutations and functional studies.
Authors: Ardon, O, et.al. .
Journal: Molecular genetics and metabolism reports (Unknown Journal), Vol. 8, 2016 .
Snippet: The second patient had a three base pair deletion in the SLC6A8 gene (c.1222_1224delTTC,
Affiliation: Research and Development, ARUP Laboratories, Salt Lake City, UT, USA; Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT, USA; Department of Pathology, University of Utah, Salt Lake City, UT, USA. Research and Development, ARUP Laboratories, Salt Lake City, UT, USA. Edmond and Lily Safra Children's hospital and Sackler Faculty of Medicine, TAU, Sheba Medical Center, Israel. Edmond and Lily Safra Children's hospital and Sackler Faculty of Medicine, TAU, Sheba Medical Center, Israel; Pediatric Neurology Unit, Edmond and Lily Safra Children's Hospital and The Dr. Pinchas Borenstein Talpiot Medical Leadership Program, Sheba Medical Center, Tel-Hashomer, Israel. Department of Pathology, University of Utah, Salt Lake City, UT, USA; Edmond and Lily Safra Children's hospital and Sackler Faculty of Medicine, TAU, Sheba Medical Center, Israel. .
Related Products: order online
14: Title: Creatine transporter deficiency leads to increased whole body and cellular metabolism.
Authors: Perna, Marla K, et.al. .
Journal: Amino acids, Vol. 48 (8): 2057-65, 2016 .
Snippet: In humans, mutations in the Cr transporter (CRT;SLC6A8) prevent Cr entry into tissue and result in a significant intellectual impairment, epilepsy, and aphasia.
Affiliation: Division of Neurology, Cincinnati Children's Research Foundation, 3333 Burnet Ave, ML 7044, Cincinnati, OH, 45229, USA. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, USA. Department of Neurology, University of Cincinnati College of Medicine, Cincinnati, USA. Department of Neurosurgery, University of Cincinnati College of Medicine, Cincinnati, USA. Heart Institute, Cincinnati Children's Research Foundation, Cincinnati, USA. Division of Neurology, Cincinnati Children's Research Foundation, 3333 Burnet Ave, ML 7044, Cincinnati, OH, 45229, USA. matthew.skelton@cchmc.org. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, USA. matthew.skelton@cchmc.org. .
Related Products: order online
15: Title: Impaired muscle uptake of creatine in spinal and bulbar muscular atrophy.
Authors: Hijikata, Yasuhiro, et.al. .
Journal: Annals of clinical and translational neurology (Unknown Journal), Vol. 3 (7): 537-46, 2016 .
Snippet: Furthermore, we measured the mRNA expression levels of SLC6A8 in cultured muscle cells (C2C12) transfected with the polyglutamine-expanded androgen receptor (AR-97Q).
Affiliation: Department of Neurology Nagoya University Graduate School of Medicine Nagoya Japan. Department of NeurologyNagoya University Graduate School of MedicineNagoyaJapan; Innovation Center for Clinical ResearchNational Center for Geriatrics and GerontologyObuJapan. Department of NeurologyNagoya University Graduate School of MedicineNagoyaJapan; Institute for Advanced ResearchNagoya UniversityNagoyaJapan. Biostatistics Section, Center for Advanced Medicine and Clinical Research Nagoya University Graduate School of Medicine Nagoya Japan. Department of NeurologyNagoya University Graduate School of MedicineNagoyaJapan; Department of NeurologyUniversity of Occupational and Environmental Health School of MedicineKitakyushuJapan. Department of Speech Pathology and Audiology Aichi-Gakuin University School of Health Science Nisshin Japan. Department of NeurologyNagoya University Graduate School of MedicineNagoyaJapan; Research Division of Dementia and Neurodegenerative DiseaseNagoya University Graduate School of MedicineNagoyaJapan. .
Related Products: order online
16: Title: Creatine Transporter Deficiency: Screening of Males with Neurodevelopmental Disorders and Neurocognitive Characterization of a Case.
Authors: Thurm, Audrey, et.al. .
Journal: Journal of developmental and behavioral pediatrics : JDBP (J Dev Behav Pediatr), Vol. 37 (4): 322-6, 2016 .
Snippet: CTD is identified by elevated urine creatine/creatinine (Cr/Crn) ratio or reduced Cr peak on brain magnetic resonance spectroscopy; the diagnosis is confirmed by decreased Cr uptake in cultured fibroblasts, and/or identification of a mutation in the SLC6A8 gene.
Affiliation: *Pediatrics and Developmental Neuroscience Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD; †Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD; ‡Therapeutics for Rare and Neglected Diseases, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD; §Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT; ‖Associated Regional and University Pathologists (ARUP) Laboratories, Salt Lake City, UT; ¶Department of Pathology, University of Utah, Salt Lake City, UT; **Department of Clinical Chemistry, Metabolic Unit, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, the Netherlands. .
Related Products: order online
17: Title: Structural correlates of the creatine transporter function regulation: the undiscovered country.
Authors: Santacruz, Lucia, et.al. .
Journal: Amino acids, Vol. 48 (8): 2049-55, 2016 .
Snippet: Therefore, these cells depend on Cr uptake across the cell membrane by a specialized creatine transporter (CrT solute carrier SLC6A8) in order to maintain intracellular creatine levels.
Affiliation: Department of Biochemistry and Molecular Biology, University of Texas, Medical Branch, 301 University Boulevard, Galveston, TX, USA. lasantac@utmb.edu. Department of Biochemistry and Molecular Biology, University of Texas, Medical Branch, 301 University Boulevard, Galveston, TX, USA. Departament of Surgery and the institute for Translational Sciences, University of Texas, Medical Branch, Galveston, USA. .
Related Products: order online
18: Title: Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing.
Authors: Qin, Lan, et.al. .
Journal: The Journal of molecular diagnostics : JMD (J Mol Diagn), Vol. 18 (3): 446-53, 2016 .
Snippet: Mosaicism was identified for autosomal dominant (JAG1, COL3A1), autosomal recessive (PYGM), and X-linked (PHKA2, PDHA1, OTC, and SLC6A8) disorders.
Affiliation: Baylor Miraca Genetics Laboratories, Houston, Texas. Baylor Miraca Genetics Laboratories, Houston, Texas; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas. Division of Pediatric Endocrinology, Montreal Children's Hospital, Montreal, Quebec, Canada. Department of Pediatrics, Section of Genetics, University of Oklahoma Health Science Center, Oklahoma City, Oklahoma. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas. Baylor Miraca Genetics Laboratories, Houston, Texas; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas. Electronic address: ljwong@bcm.edu. .
Related Products: order online
19: Title: Creatine synthesis and exchanges between brain cells: What can be learned from human creatine deficiencies and various experimental models?
Authors: Hanna-El-Daher, Layane, et.al. .
Journal: Amino acids, Vol. 48 (8): 1877-95, 2016 .
Snippet: It has also been shown that SLC6A8 is expressed by microcapillary endothelial cells at the blood-brain barrier, but is absent from surrounding astrocytes, raising the concept that the blood-brain barrier has a limited permeability for peripheral creatine.
Affiliation: Service of Biomedicine, Neurometabolic Unit, Lausanne University Hospital, 1011, Lausanne, Switzerland. Service of Biomedicine, Neurometabolic Unit, Lausanne University Hospital, 1011, Lausanne, Switzerland. Olivier.Braissant@chuv.ch. .
Related Products: order online
20: Title: Fenugreek increases insulin-stimulated creatine content in L6C11 muscle myotubes.
Authors: Tomcik, Kristyen A, et.al. .
Journal: European journal of nutrition (Eur J Nutr), Vol. 56 (3): 973-979, 2017 .
Snippet: Alterations in the expression of the sodium- and chloride-dependent creatine transporter, SLC6A8, and key signaling proteins in the PI3-K/Akt pathway were determined.
Affiliation: Centre for Exercise and Nutrition, Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, VIC, 3065, Australia. School of Applied Sciences and Health Innovations Research Institute, RMIT University, Melbourne, VIC, Australia. Centre for Exercise and Nutrition, Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, VIC, 3065, Australia. john.hawley@acu.edu.au. Research Institute for Sports and Exercise Sciences, Liverpool John Moores University, Liverpool, UK. john.hawley@acu.edu.au. .
Related Products: order online
Page 1 2 3 … 9 
Documents per page: 20 | 50 | 100