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1دورية أكاديمية
المصدر: Frontiers in Neurology, Vol 13 (2022)
مصطلحات موضوعية: locomotor training, paired associative stimulation (PAS), rehabilitation, spinal cord injury (SCI), transspinal stimulation, transspinal evoked potentials (TEPs), Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2022.1000940/fullTest; https://doaj.org/toc/1664-2295Test
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2دورية أكاديمية
المؤلفون: Carolin Rickert, Monika Grabowski, Georg Gosheger, Dominik Schorn, Kristian Nikolaus Schneider, Sebastian Klingebiel, Dennis Liem
المصدر: BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-6 (2020)
مصطلحات موضوعية: Shoulder immobilization, Activity of daily living, Sedentary behavior, Rehabilitation, Diseases of the musculoskeletal system, RC925-935
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s12891-020-3133-8Test; https://doaj.org/toc/1471-2474Test
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3دورية أكاديمية
المؤلفون: Timothy S. Pulverenti, Morad Zaaya, Monika Grabowski, Ewelina Grabowski, Md. Anamul Islam, Jeffrey Li, Lynda M. Murray, Maria Knikou
المصدر: Frontiers in Neurology, Vol 12 (2021)
مصطلحات موضوعية: H-reflex, locomotor training, neuromodulation, paired associative stimulation, rehabilitation, spinal cord injury, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2021.627975/fullTest; https://doaj.org/toc/1664-2295Test
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4
المؤلفون: Monika Grabowski, Udo Koehler, Elke Holinski-Feder, Ulrike Bacher
المصدر: Cancer Genetics and Cytogenetics. 175:81-84
مصطلحات موضوعية: Adult, Male, Cancer Research, Biology, MLH1, DNA-binding protein, Genetics, medicine, Humans, Nuclear protein, Interphase, Molecular Biology, In Situ Hybridization, Fluorescence, Adaptor Proteins, Signal Transducing, Aged, Chromosome Aberrations, Gene Rearrangement, medicine.diagnostic_test, Nuclear Proteins, Gene rearrangement, Middle Aged, Colorectal Neoplasms, Hereditary Nonpolyposis, DNA-Binding Proteins, MSH6, Mutation, Mutation (genetic algorithm), Cancer research, Female, MutL Protein Homolog 1, Microsatellite Repeats, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a017551cf9a6f2d74b5e2bb0fc202f9Test
https://doi.org/10.1016/j.cancergencyto.2007.01.008Test -
5
المؤلفون: Peter Lohse, Reinhard Kopp, Uwe Schiemann, Jens Daum, Monika Grabowski, Yvonne Mueller-Koch, Brigitte Kerker, Manfred Gross, Elke Holinski-Feder, Gisela Keller, Gabriele Henke, Holger Vogelsang, Daniela E. Aust, Michael H. Muders, Ingrid Becker, Michael Scholz
المصدر: Gut. 54:1733-1740
مصطلحات موضوعية: Adult, Male, Oncology, medicine.medical_specialty, Pathology, Letter, Familial Colorectal Cancer Type X, Colorectal cancer, Molecular evidence, MLH1, Neoplastic Syndromes, Hereditary, Internal medicine, medicine, Humans, Age of Onset, Adaptor Proteins, Signal Transducing, Splenic flexure, business.industry, Gastroenterology, Nuclear Proteins, Nucleic Acid Hybridization, Microsatellite instability, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Neoplasm Proteins, Pedigree, MutS Homolog 2 Protein, MSH2, Population Surveillance, Mutation, Disease Progression, Female, Age of onset, Carrier Proteins, MutL Protein Homolog 1, business, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c2d64f135a0c175933534ef99f8abc8Test
https://doi.org/10.1136/gut.2004.060905Test -
6The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted
المؤلفون: Monika Grabowski, Friedrich Asmus, Thomas Meitinger, Vera M. Kalscheuer, Alexander Zimprich, Bettina Lorenz-Depiereux, Tim M. Strom, Thomas Gasser
المصدر: Eur. J. Hum. Genet. 11, 138-144 (2003)
مصطلحات موضوعية: Male, Myoclonus, Biology, Cytosine, Genomic Imprinting, Exon, SGCE, Sarcoglycans, Genetics, Humans, Allele, Imprinting (psychology), Genetics (clinical), Membrane Glycoproteins, Wild type, Sequence Analysis, DNA, Penetrance, Pedigree, Cytoskeletal Proteins, myoclonus-dystonia syndrome, epsilon-sarcoglycan, imprinting, differential methylation, CpG site, Dystonic Disorders, 5-Methylcytosine, CpG Islands, Female, Genomic imprinting
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d12d476987d9b4476ec8ca52c5cd11Test
https://doi.org/10.1038/sj.ejhg.5200938Test -
7
المؤلفون: Peter Kern, Bertram Müller-Myhsok, Tanja Müller, Tim M. Strom, Thomas Meitinger, Mirna Castro, Daniela Berg, M. Bertram, Friedrich Asmus, Markus Naumann, Monika Grabowski, Thomas Gasser, Alexander Zimprich, Karl Scheidtmann, Matthias F. Bauer, Leonhard Riedel, Juliane Winkelmann
المصدر: Nature Genetics. 29:66-69
مصطلحات موضوعية: Genetics, Dystonia, Positional cloning, Locus (genetics), Myoclonic dystonia, Biology, medicine.disease, Penetrance, nervous system diseases, SGCE, medicine, medicine.symptom, Allele, Myoclonus
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::237093fcb03ec2f3cdc2c5a7c5ebce5bTest
https://doi.org/10.1038/ng709Test -
8
المؤلفون: Michael J. Econs, Thomas Meitinger, Kenneth E. White, Bettina Lorenz-Depiereux, Tim M. Strom, Monika Grabowski, Jeffery L.H. O'Riordan, Marcy C. Speer, Wayne E. Evans
المصدر: Nature Genetics. 26:345-348
مصطلحات موضوعية: Male, Fibroblast growth factor 23, medicine.medical_specialty, Positional cloning, DNA Mutational Analysis, Molecular Sequence Data, Autosomal dominant hypophosphatemic rickets, Biology, Genetic Heterogeneity, Internal medicine, Genetics, medicine, Humans, Point Mutation, Abnormalities, Multiple, Amino Acid Sequence, Hypophosphatemia, Familial, Genes, Dominant, Chromosomes, Human, Pair 12, Sequence Homology, Amino Acid, Reverse Transcriptase Polymerase Chain Reaction, PHEX, X-linked hypophosphatemia, medicine.disease, United States, Pedigree, Europe, Fibroblast Growth Factors, Familial Hypophosphatemic Rickets, Fibroblast Growth Factor-23, Hypophosphatemic Rickets, Endocrinology, Genes, Female, Lod Score, Renal phosphate excretion, Sequence Alignment
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e30b3bb5b736134d4fcab55d2df117Test
https://doi.org/10.1038/81664Test -
9
المؤلفون: Wolfgang Dietmaier, Elke Holinski-Feder, Arndt Hartmann, Gisela Keller, Stephan Dechant, Petra Ruemmele, Ferdinand Hofstaedter, Marcus Bettstetter, Monika Grabowski
المصدر: Clinical cancer research : an official journal of the American Association for Cancer Research. 13(11)
مصطلحات موضوعية: Adult, Proto-Oncogene Proteins B-raf, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Colorectal cancer, Biology, MLH1, medicine.disease_cause, Cohort Studies, Diagnosis, Differential, medicine, Humans, Promoter Regions, Genetic, neoplasms, Adaptor Proteins, Signal Transducing, Aged, Genetics, Mutation, Reverse Transcriptase Polymerase Chain Reaction, nutritional and metabolic diseases, Microsatellite instability, Nuclear Proteins, Methylation, DNA Methylation, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Lynch syndrome, Oncology, DNA methylation, Cancer research, DNA mismatch repair, Colorectal Neoplasms, MutL Protein Homolog 1, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0cf0ddc91e454bcdf57f180eb3c4156Test
https://pubmed.ncbi.nlm.nih.gov/17545526Test -
10
المؤلفون: Elke Holinski-Feder, Maria Gruber, Wolfgang Schmitt, Christa Doerner, Birgit Neitzel, Yvonne Mueller-Koch, Petra Ruemmele, Udo Koehler, Monika Grabowski, Brigitte Kerker, Wolfgang Dietmaier, Eva Grasbon-Frodl, Ulrike Siebers, Gisela Keller, Gabriele Henke, Holger Vogelsang, Reinhard Kopp
المصدر: Genetic testing. 9(2)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Biology, MLH1, Alu Elements, Gene Duplication, medicine, PMS2, Humans, Point Mutation, Multiplex ligation-dependent probe amplification, neoplasms, Genetics (clinical), In Situ Hybridization, Fluorescence, Sequence Deletion, Genetics, Base Sequence, Point mutation, nutritional and metabolic diseases, Microsatellite instability, Exons, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, digestive system diseases, MSH6, MSH2, DNA mismatch repair, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::386ad53b7cc9a42b63ce047dcdb72a4bTest
https://pubmed.ncbi.nlm.nih.gov/15943554Test