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Wyświetlanie 1-16 z 16
Tytuł :
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.
Autorzy :
Radio FC; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Pang K; Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
Ciolfi A; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Levy MA; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.
Hernández-García A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Pedace L; Oncohaematology Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Pantaleoni F; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Liu Z; Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
de Boer E; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 GA Nijmegen, the Netherlands.
Jackson A; Division of Evolution & Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, M13 9 WL Manchester, UK; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Bruselles A; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
McConkey H; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.
Stellacci E; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Lo Cicero S; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Motta M; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Carrozzo R; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Dentici ML; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
McWalter K; GeneDx, Gaithersburg, MD 20877, USA.
Desai M; GeneDx, Gaithersburg, MD 20877, USA.
Monaghan KG; GeneDx, Gaithersburg, MD 20877, USA.
Telegrafi A; GeneDx, Gaithersburg, MD 20877, USA.
Philippe C; Inserm UMR 1231 GAD (Génétique des Anomalies du Développement), Université de Bourgogne, 21070 Dijon, France; UF Innovation en Diagnostic Génomique des Maladies Rares, CHU, Dijon Bourgogne, 21079 Dijon, France.
Vitobello A; Inserm UMR 1231 GAD (Génétique des Anomalies du Développement), Université de Bourgogne, 21070 Dijon, France; UF Innovation en Diagnostic Génomique des Maladies Rares, CHU, Dijon Bourgogne, 21079 Dijon, France.
Au M; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Grand K; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Sanchez-Lara PA; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Baez J; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Lindstrom K; Phoenix Children's Hospital, Phoenix, AZ 85016, USA.
Kulch P; Phoenix Children's Hospital, Phoenix, AZ 85016, USA.
Sebastian J; Division of Medical Genetics, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, USA.
Madan-Khetarpal S; Division of Medical Genetics, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA 15224, USA.
Roadhouse C; McMaster Children's Hospital, Hamilton, ON L8N 3Z5, Canada.
MacKenzie JJ; McMaster Children's Hospital, Hamilton, ON L8N 3Z5, Canada.
Monteleone B; Clinical genetics, NYU Langone Long Island School of Medicine, Mineola, NY 11501, USA.
Saunders CJ; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Jean Cuevas JK; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Cross L; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Zhou D; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Hartley T; Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.
Sawyer SL; Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.
Monteiro FP; Mendelics Genomic Analysis, Campo Belo - São Paulo 04013-000, Brazil.
Secches TV; Mendelics Genomic Analysis, Campo Belo - São Paulo 04013-000, Brazil.
Kok F; Mendelics Genomic Analysis, Campo Belo - São Paulo 04013-000, Brazil.
Schultz-Rogers LE; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Macke EL; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Morava E; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA; Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55905, USA.
Klee EW; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Kemppainen J; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Iascone M; Ospedale Papa Giovanni XXIII, 24127 Bergamo, Italy.
Selicorni A; Azienda Socio Sanitaria Territoriale Lariana, 22100 Como, Italy.
Tenconi R; Dipartimento di Pediatria, Università di Padova, 35137 Padua, Italy.
Amor DJ; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia; Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
Pais L; Medical and Populations Genetics Program, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Gallacher L; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia; Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
Turnpenny PD; Royal Devon & Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.
Stals K; Royal Devon & Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.
Ellard S; Royal Devon & Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.
Cabet S; Department of Genetics, Hospices Civils de Lyon, Groupement Hospitalier Est, Claude Bernard Lyon 1 University, 69002 Lyon, France.
Lesca G; Department of Genetics, Hospices Civils de Lyon, Groupement Hospitalier Est, Claude Bernard Lyon 1 University, 69002 Lyon, France.
Pascal J; Institute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Steindl K; Institute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Ravid S; Pediatric Neurology Unit, Ruth Children's Hospital, Rambam Health Care Campus, Haifa 3109601, Israel.
Weiss K; Genetics Institute, Rambam Health Care Campus, Rappaport Faculty of Medicine, Israel Institute of Technology, Haifa 3109601, Israel.
Castle AMR; Department of Genetics, CHEO, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Carter MT; Department of Genetics, CHEO, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Kalsner L; Connecticut Children's Medical Center, University of Connecticut School of Medicine, Farmington, CT 06032, USA.
de Vries BBA; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 GA Nijmegen, the Netherlands.
van Bon BW; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands.
Wevers MR; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands.
Pfundt R; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands.
Stegmann APA; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Department of Clinical Genetics, Maastricht University Medical Center+, 6229 HX Maastricht, the Netherlands.
Kerr B; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Kingston HM; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Chandler KE; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Sheehan W; Department of Medical Genetics, Shodair Children's Hospital, Helena, MT 59601, USA.
Elias AF; Department of Medical Genetics, Shodair Children's Hospital, Helena, MT 59601, USA.
Shinde DN; Ambry Genetics, Aliso Viejo, CA 92656, USA.
Towne MC; Ambry Genetics, Aliso Viejo, CA 92656, USA.
Robin NH; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Goodloe D; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Vanderver A; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Sherbini O; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Bluske K; Illumina Clinical Services Laboratory, San Diego, CA 92122, USA.
Hagelstrom RT; Illumina Clinical Services Laboratory, San Diego, CA 92122, USA.
Zanus C; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy.
Faletra F; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy.
Musante L; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy.
Kurtz-Nelson EC; Department of Psychiatry & Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Earl RK; Department of Psychiatry & Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Anderlid BM; Department of Molecular Medicine and Surgery, Karolinska Institutet and Department of Clinical Genetics, Karolinska University Hospital, 17176 Stockholm, Sweden.
Morin G; CA de Génétique Clinique & Oncogénétique, CHU Amiens-Picardie, 80054 Amiens, France.
van Slegtenhorst M; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Diderich KEM; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Brooks AS; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Gribnau J; Department of Developmental Biology, Oncode Institute, Erasmus MC, University Medical Center, 3015 GD Rotterdam, the Netherlands.
Boers RG; Department of Developmental Biology, Oncode Institute, Erasmus MC, University Medical Center, 3015 GD Rotterdam, the Netherlands.
Finestra TR; Department of Developmental Biology, Oncode Institute, Erasmus MC, University Medical Center, 3015 GD Rotterdam, the Netherlands.
Carter LB; Department of Pediatrics, Division of Medical Genetics, Levine Children's Hospital Atrium Health, Charlotte, NC 28203, USA.
Rauch A; Institute of Medical Genetics, University of Zurich, 8952 Schlieren, Zurich, Switzerland.
Gasparini P; Institute for Maternal and Child Health, IRCCS 'Burlo Garofolo,' 34137 Trieste, Italy; Department of Medicine, Surgery & Health Science, University of Trieste, 34143 Trieste, Italy.
Boycott KM; Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.
Barakat TS; Department of Clinical Genetics, Erasmus MC University Medical Center, 3015 GD Rotterdam, the Netherlands.
Graham JM Jr; Division of Medical Genetics, Department of Pediatrics, Cedars Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90048, USA.
Faivre L; Centre de Référence Maladies Rares « Anomalies du Développement et Syndromes Malformatifs », Centre de Génétique, FHU-TRANSLAD et Institut GIMI, 77908 Dijon, France; UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, 77908 Dijon, France.
Banka S; Division of Evolution & Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, M13 9 WL Manchester, UK; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, M13 9WL Manchester, UK.
Wang T; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
Priolo M; UOSD Genetica Medica del Grande Ospedale Metropolitano 'Bianchi Melacrino Morelli' di Reggio Calabria, 89124 Reggio Calabria, Italy.
Dallapiccola B; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Vissers LELM; Department of Human Genetics, Radboudumc, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 GA Nijmegen, the Netherlands.
Sadikovic B; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.
Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.
Holder JL Jr; Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
Tartaglia M; Genetics and Rare Disease Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy. Electronic address: .
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Źródło :
American journal of human genetics [Am J Hum Genet] 2021 Mar 04; Vol. 108 (3), pp. 502-516. Date of Electronic Publication: 2021 Feb 16.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Disorders/*genetics
Chromosomes, Human, Pair 1/*genetics
Chromosomes, Human, X/*genetics
DNA-Binding Proteins/*genetics
RNA-Binding Proteins/*genetics
Adolescent ; Autism Spectrum Disorder/genetics ; Autism Spectrum Disorder/pathology ; Child ; Child, Preschool ; Chromosome Deletion ; Chromosome Disorders/physiopathology ; DNA Methylation/genetics ; Epigenesis, Genetic/genetics ; Female ; Haploinsufficiency/genetics ; Humans ; Intellectual Disability/genetics ; Intellectual Disability/physiopathology ; Male ; Neurodevelopmental Disorders/genetics ; Neurodevelopmental Disorders/physiopathology ; Phenotype ; Young Adult
SCR Disease Name :
Chromosome 1p36 Deletion Syndrome
Czasopismo naukowe
Tytuł :
Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy.
Autorzy :
Carter LB; Stanford University, Stanford, California.
Battaglia A; Department of Developmental Neuroscience, IRCCS Stella Maris Foundation, Pisa, Italy.
Cherry A; Stanford University, Stanford, California.
Manning MA; Stanford University, Stanford, California.
Ruzhnikov MR; Stanford University, Stanford, California.
Bird LM; University of California San Diego and Rady Children's Hospital San Diego, San Diego, California.
Dowsett L; Kapi'olani Medical Center and University of Hawai'i, Honolulu, Hawaii.
Graham JM Jr; Cedars-Sinai Medical Center, Los Angeles, California.
Alkuraya FS; King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Hashem M; King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Dinulos MB; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Vallee S; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Adam MP; University of Washington, Seattle, Washington.
Glass I; University of Washington, Seattle, Washington.
Beck AE; University of Washington, Seattle, Washington.
Stevens CA; University of Tennessee School of Medicine, Knoxville, Tennessee.
Zackai E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
McDougall C; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Keena B; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Peron A; Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.; Department of Pediatrics, Division of Medical Genetics, University of Utah School of Medicine, Salt Lake City, Utah.
Vignoli A; Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Seaver LH; Spectrum Health Helen DeVos Children's Hospital.; Michigan State University Department of Pediatrics and Human Development, Grand Rapids, Michigan.
Slavin TP; Division of Clinical Cancer Genomics, City of Hope, Duarte, California.
Hudgins L; Stanford University, Stanford, California.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2019 Aug; Vol. 179 (8), pp. 1543-1546. Date of Electronic Publication: 2019 Jun 17.
Typ publikacji :
Journal Article; Meta-Analysis; Review
MeSH Terms :
Phenotype*
Psychological Distress*
Chromosome Disorders/*diagnosis
Chromosome Disorders/*genetics
Hypoxia-Ischemia, Brain/*diagnosis
Chromosome Deletion ; Chromosomes, Human, Pair 1/genetics ; Diagnosis, Differential ; Female ; Humans ; Infant, Newborn ; Male ; Pregnancy
SCR Disease Name :
Chromosome 1p36 Deletion Syndrome
Czasopismo naukowe
Tytuł :
Smokers Display Reduced Glucocorticoid Sensitivity Prior to Symptomatic Chronic Disease Development.
Autorzy :
Bennett JM; Department of Psychological Science, UNC Charlotte, NC, USA.; Health Psychology PhD Program, UNC Charlotte, NC, USA.
Marino JS; Department of Kinesiology, Laboratory of Systems Physiology, UNC Charlotte, NC, USA.
Peck B; Department of Kinesiology, Laboratory of Systems Physiology, UNC Charlotte, NC, USA.
Roos LG; Health Psychology PhD Program, UNC Charlotte, NC, USA.
Joseph KM; Department of Psychological Science, UNC Charlotte, NC, USA.
Carter LB; Department of Psychological Science, UNC Charlotte, NC, USA.
Smith CB; School of Nursing, UNC Charlotte, NC, USA.
Rohleder N; Department of Psychology and Sports Science, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany.; Department of Psychology, Brandeis University, MA, USA.
Coffman MJ; Health Psychology PhD Program, UNC Charlotte, NC, USA.; School of Nursing, UNC Charlotte, NC, USA.
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Źródło :
Annals of behavioral medicine : a publication of the Society of Behavioral Medicine [Ann Behav Med] 2018 Sep 13; Vol. 52 (10), pp. 830-841.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Cigarette Smoking/*adverse effects
Cigarette Smoking/*immunology
Glucocorticoids/*pharmacology
Leukocytes, Mononuclear/*drug effects
Leukocytes, Mononuclear/*immunology
Adult ; Chronic Disease ; Female ; Humans ; Male
Czasopismo naukowe
Tytuł :
Clinical anesthesia causes permanent damage to the fetal guinea pig brain.
Autorzy :
Rizzi S; Department of Anesthesiology, University of Virginia Health System, Charlottesville, VA 22908, USA.
Carter LB
Ori C
Jevtovic-Todorovic V
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Źródło :
Brain pathology (Zurich, Switzerland) [Brain Pathol] 2008 Apr; Vol. 18 (2), pp. 198-210. Date of Electronic Publication: 2008 Jan 29.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Prenatal Exposure Delayed Effects*
Anesthesia/*adverse effects
Brain Damage, Chronic/*etiology
Animals ; Brain/pathology ; Brain Damage, Chronic/pathology ; Disease Models, Animal ; Embryo, Mammalian ; Female ; Guinea Pigs ; Male ; Pregnancy
Czasopismo naukowe
Tytuł :
Early exposure to general anesthesia causes significant neuronal deletion in the developing rat brain.
Autorzy :
Nikizad H; Department of Anesthesiology, University of Virginia Health System, P.O. Box 800710, Charlottesville, VA 22980, USA.
Yon JH
Carter LB
Jevtovic-Todorovic V
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Źródło :
Annals of the New York Academy of Sciences [Ann N Y Acad Sci] 2007 Dec; Vol. 1122, pp. 69-82.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Anesthetics, Inhalation/*adverse effects
Apoptosis/*drug effects
Brain/*cytology
Brain/*growth & development
Neurons/*drug effects
Animals ; Animals, Newborn ; Gene Expression Regulation, Developmental/drug effects ; Nerve Tissue Proteins/metabolism ; Rats ; Rats, Sprague-Dawley ; Time Factors
Czasopismo naukowe
Tytuł :
General anesthesia activates BDNF-dependent neuroapoptosis in the developing rat brain.
Autorzy :
Lu LX; Department of Anasthesiology, University of Virginia Health System, P.O. Box 800710, Charlottesville, 22908, USA.
Yon JH
Carter LB
Jevtovic-Todorovic V
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Źródło :
Apoptosis : an international journal on programmed cell death [Apoptosis] 2006 Sep; Vol. 11 (9), pp. 1603-15.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Anesthesia, General/*adverse effects
Apoptosis/*drug effects
Brain/*growth & development
Brain-Derived Neurotrophic Factor/*physiology
Neurons/*drug effects
Anesthetics/adverse effects ; Anesthetics/pharmacology ; Animals ; Apoptosis/physiology ; Brain/drug effects ; Brain-Derived Neurotrophic Factor/metabolism ; Cerebral Cortex/drug effects ; Cerebral Cortex/growth & development ; Down-Regulation/drug effects ; Estradiol/pharmacology ; Models, Biological ; Nerve Degeneration/chemically induced ; Oncogene Protein v-akt/metabolism ; Oncogene Proteins/metabolism ; Rats ; Rats, Sprague-Dawley ; Respiratory Insufficiency/chemically induced ; Signal Transduction/drug effects ; Thalamus/drug effects ; Thalamus/growth & development
Czasopismo naukowe
Tytuł :
Neurotoxicity of nitrous oxide and ketamine is more severe in aged than in young rat brain.
Autorzy :
Beals JK; Department of Anesthesiology, University of Virginia Health System, Charlottesville 22908, USA.
Carter LB
Jevtovic-Todorovic V
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Źródło :
Annals of the New York Academy of Sciences [Ann N Y Acad Sci] 2003 May; Vol. 993, pp. 115; discussion 123-4.
Typ publikacji :
Journal Article; Research Support, U.S. Gov't, P.H.S.
MeSH Terms :
Aging/*physiology
Anesthetics, Dissociative/*toxicity
Anesthetics, Inhalation/*toxicity
Cerebral Cortex/*drug effects
Ketamine/*toxicity
Nitrous Oxide/*toxicity
Anesthetics, Dissociative/pharmacology ; Anesthetics, Inhalation/pharmacology ; Animals ; Cerebral Cortex/physiology ; Female ; Ketamine/pharmacology ; Nitrous Oxide/pharmacology ; Rats ; Rats, Inbred F344 ; Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors
Czasopismo naukowe
Tytuł :
Renal function in patients receiving long-term lithium therapy.
Autorzy :
Uldall PR
Awad AG
McCormick WO
Carter LB
Gonsick T
Grass CL
Kugelmass MI
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Źródło :
Canadian Medical Association journal [Can Med Assoc J] 1981 Jun 01; Vol. 124 (11), pp. 1471-4.
Typ publikacji :
Journal Article
MeSH Terms :
Kidney/*drug effects
Kidney Diseases/*chemically induced
Lithium/*adverse effects
Female ; Glomerular Filtration Rate/drug effects ; Humans ; Hydrogen-Ion Concentration ; Kidney Concentrating Ability/drug effects ; Male ; Mental Disorders/drug therapy ; Time Factors
Czasopismo naukowe
Tytuł :
Cognitive learning and anxiety in registered nurses in CEU-contingent and noncontingent continuing education courses.
Autorzy :
Carter LB
Mills GC
Pokaż więcej
Źródło :
Journal of continuing education in nursing [J Contin Educ Nurs] 1982 May-Jun; Vol. 13 (3), pp. 19-27.
Typ publikacji :
Journal Article
MeSH Terms :
Anxiety*
Education, Nursing, Continuing*
Learning*
Students, Nursing/*psychology
Education, Nursing, Diploma Programs ; Educational Measurement ; Humans ; Psychological Tests
Czasopismo naukowe
    Wyświetlanie 1-16 z 16

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