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1
المؤلفون: Roseline Caume, M Scott Perry, Massimo Mastrangelo, Margarete Koch-Hogrebe, Pasquale Striano, Karen Müller-Schlüter, Petra Laššuthová, Monisa D. Wagner, Ingo Helbig, Stephan Lauxmann, Emmanuel Scalais, Marie-Cécile Nassogne, Silvia Masnada, Henrike O. Heyne, Konrad Platzer, Frederic Bilan, Chloe A Stutterd, Sonja Walsh, Katrine M Johannesen, Damien Lederer, Ngoc Minh Le, Christina Fenger, Daniel Tibussek, Lukas Sonnenberg, Andrea Berger, Yuanyuan Liu, Mikhail Abramov, Karen E. Wain, Sergey Korostelev, P Y Billie Au, Elena L. Dadali, An-Sofie Schoonjans, Cornelia Betzler, Artem Borovikov, Johanna Krüger, Maert Rannap, Sebastian Lebon, Nils A Koch, Nancy Eisenhauer, Judith Kroell-Seger, Julian Schubert, Marije Meuwissen, Caroline Lund, Mark Fitzgerald, Federico Zara, Siddharth Srivastava, Claudia M Bonardi, Pia Zacher, Haim Bassan, Arve Vøllo, Katherine B. Howell, Francesca Darra, Guido Rubboli, Stephen W. Scherer, Bénédicte Gérard, Stefano Sartori, Annapurna Poduri, Helene Verhelst, Katalin Sterbova, Mathilde Nizon, Marketa Vlckova, Christina E. Hoei-Hansen, Renzo Guerrini, Ilya V. Kanivets, Juliann M. Savatt, Johannes Rebstock, Jakob Christensen, Cecilia Altuzarra, Dennis Lal, Judith S. Verhoeven, Agathe Roubertie, Constanze Heine, Dagmar Wieczorek, Ingo Borggraefe, Aster V. E. Harder, Anne Destrée, Wen-Hann Tan, Tobias Brünger, Shoji Ichikawa, Laura Canafoglia, Mahmoud Koko, Sergey Kutsev, Sabine Grønborg, Patrizia Accorsi, Heather E. Olson, Bert van der Zwaag, Cathrine E Gjerulfsen, Patrick May, A. A. Sharkov, M. Mahdi Motazacker, Manuela Pendziwiat, Richard J. Leventer, Anna Jansen, Lucio Giordano, Holger Lerche, Carla Marini, Karl Martin Klein, Eva H. Brilstra, Ahmed Eltokhi, Ethan M. Goldberg, Walid Fazeli, Rikke S. Møller, Dorota Hoffman-Zacharska, Michael Alber, Susanne Ruf, Jennifer L. Howe, Phillis Lakeman, Josua Kegele, Katherine L. Helbig, Marga Buzatu, Alice W Ho, Jan Benda, Ilona Krey, Marion Gérard, Sara Matricardi, Thomas U. Mayer, Philippe Gelisse, Jong M. Rho, Johannes R. Lemke, Pierangelo Veggiotti, Tobias Loddenkemper, Gaetan Lesca, Ulrike B. S. Hedrich, Silvana Franceschetti, Elena Gardella, Irina Mishina, María Vaccarezza, Timo Roser
المساهمون: Public Health Sciences, Mental Health and Wellbeing research group, Neurogenetics, Neuroprotection & Neuromodulation, Pediatrics, Human Genetics, ANS - Complex Trait Genetics, ARD - Amsterdam Reproduction and Development, Human genetics, Amsterdam Reproduction & Development (AR&D)
المصدر: Johannesen, K M, Liu, Y, Koko, M, Gjerulfsen, C E, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N A, Lauxmann, S, Krüger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthová, P, Vlckova, M, Lemke, J R, Platzer, K, Krey, I, Heine, C, Wieczorek, D, Kroell-Seger, J, Lund, C, Klein, K M, Au, P Y B, Rho, J M, Ho, A W, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoei-Hansen, C E, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, Braakman, H M H, van der Zwaag, B, Harder, A V E, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, Le, N M, Christensen, J, Grønborg, S, Scherer, S W, Howe, J, Fazeli, W, Howell, K B, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vøllo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caume, R, Roubertie, A, Gélisse, P, Marini, C, Guerrini, R, Bilan, F, Tibussek, D, Koch-Hogrebe, M, Perry, M S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J M, Müller-Schlüter, K, Bassan, H, Borovikov, A, Nassogne, M C, Destrée, A, Schoonjans, A S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W H, Olson, H E, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M P, Goldberg, E M, Roser, T, Borggraefe, I, Brünger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Heyne, H O, Lesca, G, Hedrich, U B S, Benda, J, Gardella, E, Lerche, H & Møller, R S 2022, ' Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications ', Brain, vol. 145, no. 9, pp. 2991-3009 . https://doi.org/10.1093/brain/awab321
Johannesen, K M, Liu, Y, Koko, M, Gjerulfsen, C E, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N A, Lauxmann, S, Krüger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthová, P, Vlckova, M, Lemke, J R, Platzer, K, Krey, I, Heine, C, Wieczorek, D, Kroell-Seger, J, Lund, C, Klein, K M, Au, P Y B, Rho, J M, Ho, A W, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoei-Hansen, C E, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, Braakman, H M H, van der Zwaag, B, Harder, A V E, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, Le, N M, Christensen, J, Grønborg, S, Scherer, S W, Howe, J, Fazeli, W, Howell, K B, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vøllo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caume, R, Roubertie, A, Gélisse, P, Marini, C, Guerrini, R, Bilan, F, Tibussek, D, Koch-Hogrebe, M, Perry, M S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J M, Müller-Schlüter, K, Bassan, H, Borovikov, A, Nassogne, M C, Destrée, A, Schoonjans, A S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W H, Olson, H E, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M P, Goldberg, E M, Roser, T, Borggraefe, I, Brünger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Heyne, H O, Lesca, G, Hedrich, U B S, Benda, J, Gardella, E, Lerche, H & Møller, R S 2022, ' Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications ', Brain : a journal of neurology, vol. 145, no. 9, pp. 2991-3009 . https://doi.org/10.1093/brain/awab321
Brain
Johannesen, K M, Liu, Y, Koko, M, Gjerulfsen, C E, Sonnenberg, L, Schubert, J, Fenger, C D, Eltokhi, A, Rannap, M, Koch, N A, Lauxmann, S, Krüger, J, Kegele, J, Canafoglia, L, Franceschetti, S, Mayer, T, Rebstock, J, Zacher, P, Ruf, S, Alber, M, Sterbova, K, Lassuthová, P, Vlckova, M, Lemke, J R, Platzer, K, Krey, I, Heine, C, Wieczorek, D, Kroell-Seger, J, Lund, C, Klein, K M, Au, P Y B, Rho, J M, Ho, A W, Masnada, S, Veggiotti, P, Giordano, L, Accorsi, P, Hoei-Hansen, C E, Striano, P, Zara, F, Verhelst, H, Verhoeven, J S, Braakman, H M H, van der Zwaag, B, Harder, A V E, Brilstra, E, Pendziwiat, M, Lebon, S, Vaccarezza, M, le, N M, Christensen, J, Grønborg, S, Scherer, S W, Howe, J, Fazeli, W, Howell, K B, Leventer, R, Stutterd, C, Walsh, S, Gerard, M, Gerard, B N, Matricardi, S, Bonardi, C M, Sartori, S, Berger, A, Hoffman-Zacharska, D, Mastrangelo, M, Darra, F, Vøllo, A, Motazacker, M M, Lakeman, P, Nizon, M, Betzler, C, Altuzarra, C, Caume, R, Roubertie, A, Gélisse, P, Marini, C, Guerrini, R, Bilan, F, Tibussek, D, Koch-Hogrebe, M, Perry, M S, Ichikawa, S, Dadali, E, Sharkov, A, Mishina, I, Abramov, M, Kanivets, I, Korostelev, S, Kutsev, S, Wain, K E, Eisenhauer, N, Wagner, M, Savatt, J M, Müller-Schlüter, K, Bassan, H, Borovikov, A, Nassogne, M C, Destrée, A, Schoonjans, A S, Meuwissen, M, Buzatu, M, Jansen, A, Scalais, E, Srivastava, S, Tan, W H, Olson, H E, Loddenkemper, T, Poduri, A, Helbig, K L, Helbig, I, Fitzgerald, M P, Goldberg, E M, Roser, T, Borggraefe, I, Brünger, T, May, P, Lal, D, Lederer, D, Rubboli, G, Heyne, H O, Lesca, G, Hedrich, U B S, Benda, J, Gardella, E, Lerche, H & Møller, R S 2022, ' Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications ', Brain, vol. 145, no. 9, pp. 2991-3009 . https://doi.org/10.1093/brain/awab321
Brain, 145(9), 2991-3009. Oxford University Pressمصطلحات موضوعية: medicine.medical_specialty, SCN8A, Gastroenterology, Epilepsy, Sodium channel blocker, Neurodevelopmental disorder, Seizures, Intellectual Disability, Internal medicine, medicine, Humans, Missense mutation, genetics, Generalized epilepsy, Genetic Association Studies, Benign familial infantile epilepsy, Generalized, business.industry, Infant, personalized medicine, Prognosis, medicine.disease, Phenotype, Settore MED/39 - Neuropsichiatria Infantile, NAV1.6 Voltage-Gated Sodium Channel, Mutation, epilepsy, Original Article, Epilepsy, Generalized, Human medicine, Neurology (clinical), Age of onset, business, Epileptic Syndromes, Sodium Channel Blockers
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75d3de186f73a35fb1500a80403bc648
https://doi.org/10.1093/brain/awab321 -
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المؤلفون: Johannes Rebstock, Bernt Popp, Anne-Christin Teichmann, Malgorzata Kalita, Johannes R. Lemke, Tobias Bartolomaeus, Chiara Klöckner, Ilona Krey, Konrad Platzer, Mathias Stiller, Martin Finzel, Gudrun Körber, Susanne Horn, Frank Brandhoff, Pia Zacher, Thomas Mayer, Rami Abou Jamra, Julia Hentschel, Anja Heinze, Diana Le Duc, Marina Nastainczyk-Wulf
المصدر: Genetics in Medicine
مصطلحات موضوعية: Adult, 0301 basic medicine, Pediatrics, medicine.medical_specialty, Article, Fragile X Mental Retardation Protein, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Intellectual Disability, Exome Sequencing, Intellectual disability, medicine, Humans, Medical diagnosis, Genetics (clinical), Exome sequencing, Aged, business.industry, medicine.disease, FMR1, Work-up, Fragile X syndrome, 030104 developmental biology, Neurodevelopmental Disorders, Karyotyping, Nuchal cord, business, 030217 neurology & neurosurgery
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3
المؤلفون: Arve Vøllo, Stephen W. Scherer, Elena Gardella, Irina Mishina, María Vaccarezza, Jennifer L. Howe, Sebastian Lebon, Josua Kegele, Gaetan Lesca, Timo Roser, Silvia Masnada, Johannes Rebstock, Marga Buzatu, Damien Lederer, Ingo Borggraefe, Tobias Brünger, Ulrike B. S. Hedrich, Sergey Korostelev, Frédéric Bilan, Ahmed Eltokhi, M. Mahdi Motazacker, Karen E. Wain, Susanne Ruf, Manuela Pendziwiat, Lukas Sonnenberg, Yuanyuan Liu, Alice W Ho, Silvana Franceschetti, Jan Benda, Ethan M. Goldberg, Helene Verhelst, Julian Schubert, Juliann M. Savatt, Mathilde Nizon, Caroline Lund, Katherine B. Howell, Tobias Loddenkemper, Katherine L. Helbig, Cornelia Betzler, Roseline Caume, Francesca Darra, Richard J. Leventer, Christina Fenger, Pierangelo Veggiotti, Ilona Krey, Nancy Eisenhauer, Andrea Berger, Pasquale Striano, Heather E. Olson, An-Sofie Schoonjans, M Scott Perry, Stephan Lauxmann, Emmanuel Scalais, Petra Laššuthová, Monisa D. Wagner, Ilya V. Kanivets, A. A. Sharkov, P Y Billie Au, Mahmoud Koko, Siddharth Srivastava, Jakob Christensen, Artem Borovikov, Mette U Schmidt-Petersen, Anna Jansen, Judith S. Verhoeven, Johanna Krüger, Claudia M Bonardi, Shoji Ichikawa, Patrick May, Sabine Grønborg, Johannes R. Lemke, Marije Meuwissen, Katalin Sterbova, Mark Fitzgerald, Lucio Giordano, Holger Lerche, Mikhail Abramov, Bénédicte Gérard, Elena L. Dadali, Cecilia Altuzarra, Aster V. E. Harder, Stefano Sartori, Katrine M Johannesen, Sergey Kutsev, Maert Rannap, Renzo Guerrini, Dagmar Wieczorek, Laura Canafoglia, Annapurna Poduri, Christina E. Hoei-Hansen, Agathe Roubertie, Nils A Koch, Karen Müller-Schlüter, Chloe A Stutterd, Ngoc Minh Le, Pia Zacher, Constanze Heine, Sonja Walsh, Carla Marini, Federico Zara, Karl Martin Klein, Eva H. Brilstra, Guido Rubboli, Walid Fazeli, Judith Kroell-Seger, Rikke S. Møller, Dorota Hoffman-Zacharska, Michael Alber, Phillis Lakeman, Massimo Mastrangelo, Margarete Koch-Hogrebe, Ingo Helbig, Daniel Tibussek, Marketa Vlckova, Anne Destrée, Wen-Hann Tan, Haim Bassan, Dennis Lal, Patrizia Accorsi, Bert van der Zwaag, Cathrine E Gjerulfsen, Marion Gérard, Sara Matricardi, Thomas U. Mayer, Philippe Gelisse, Jong M. Rho, Marie-Cécile Nassogne
مصطلحات موضوعية: medicine.medical_specialty, Benign familial infantile epilepsy, business.industry, medicine.disease, Gastroenterology, Phenotype, Epilepsy, Electrophysiology, Sodium channel blocker, Internal medicine, medicine, Missense mutation, Generalized epilepsy, business, Genotype-Phenotype Correlations
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::35d884802200fc5b70287f52bd03bbc0
https://doi.org/10.1101/2021.03.22.21253711 -
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المؤلفون: Karsten Haug, Maike Warnstedt, Alexi K. Alekov, Thomas Sander, Alfredo Ramírez, Barbara Poser, Snezana Maljevic, Simon Hebeisen, Christian Kubisch, Johannes Rebstock, Steve Horvath, Kerstin Hallmann, Joern S. Dullinger, Birgit Rau, Fritz Haverkamp, Stefan Beyenburg, Herbert Schulz, Dieter Janz, Bernd Giese, Gerhard Müller-Newen, Peter Propping, Christian E. Elger, Christoph Fahlke, Holger Lerche, Armin Heils
المصدر: Nature Genetics. 33:527-532
مصطلحات موضوعية: Adult, Family Health, Male, Heterozygote, DNA, Complementary, Microscopy, Confocal, Adolescent, Base Sequence, Reverse Transcriptase Polymerase Chain Reaction, Cell Membrane, DNA Mutational Analysis, Molecular Sequence Data, Transfection, Models, Biological, Pedigree, Electrophysiology, Microscopy, Fluorescence, Chloride Channels, Mutation, Codon, Terminator, Genetics, Humans, Epilepsy, Generalized, Female, Plasmids
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المؤلفون: Christian Bauer, Alexandra Bauch, Ines George, Hans-H. Neumayer, Johannes Rebstock, Anja Schwarz, Berthold Hocher
المصدر: Hypertension. 33:816-822
مصطلحات موضوعية: Endothelin Receptor Antagonists, Male, medicine.hormone, medicine.medical_specialty, Hypertension, Renal, Cardiac fibrosis, Blood Pressure, Rats, Inbred WKY, Intracardiac injection, Muscle hypertrophy, Renovascular hypertension, Endothelins, Heart Rate, Fibrosis, Internal medicine, Internal Medicine, medicine, Animals, Protein Precursors, Endothelin-1, Ventricular Remodeling, Receptors, Endothelin, business.industry, Receptor, Endothelin A, medicine.disease, Coronary Vessels, Receptor, Endothelin B, Rats, Endocrinology, medicine.anatomical_structure, Ventricle, cardiovascular system, business, Endothelin receptor, circulatory and respiratory physiology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::511209c64ff8ba4d8122482c02f8122b
https://doi.org/10.1161/01.hyp.33.3.816 -
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المؤلفون: Dieter Janz, Peter Propping, Gerhard Müller-Newen, Alexi K. Alekov, Stefan Beyenburg, Fritz Haverkamp, JS Dullinger, Maike Warnstedt, Ailing A. Kleefuss-Lie, Holger Lerche, Birgit Rau, Christian Kubisch, Johannes Rebstock, Karsten Haug, Waltraut Friedl, Steve Horvath, Christoph Fahlke, Kerstin Hallmann, Thomas Sander, Bernd Giese, Simon Hebeisen, Barbara Poser, Snezana Maljevic, Alfredo Ramirez, Christian E. Elger, Sven Cichon, Herbert Schulz
المصدر: Nature genetics. 41(9)
مصطلحات موضوعية: Male, Heterozygote, DNA Mutational Analysis, Computational biology, Idiopathic generalized epilepsy, Text mining, Chloride Channels, Genetics, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Genes, Dominant, CLCN2, Family Health, biology, business.industry, Genetic Variation, medicine.disease, DNA Fingerprinting, Pedigree, CLC-2 Chloride Channels, Electrophysiology, biology.protein, Epilepsy, Generalized, Female, business
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المؤلفون: Rolf Schröder, Wolfram S. Kunz, Armin Heils, Dagmar Kunz, Johannes Rebstock, Karsten Haug, Alexei P. Kudin, Stefan Vielhaber, Dmitry A. Varlamov, Robert Sassen, Christian E. Elger, Albert J. Becker
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Mitochondrial DNA, Adolescent, Mutant, DNA Mutational Analysis, Molecular Sequence Data, Drug Resistance, Mutation, Missense, Cytochrome-c Oxidase Deficiency, Epilepsy, Partial, Motor, Mitochondrion, Gene mutation, DNA, Mitochondrial, Oxidative Phosphorylation, Electron Transport Complex IV, Enzyme Stability, Genetics, medicine, Cytochrome c oxidase, Missense mutation, Animals, Humans, Amino Acid Sequence, Muscle, Skeletal, Molecular Biology, Genetics (clinical), Conserved Sequence, biology, Base Sequence, Sequence Homology, Amino Acid, Point mutation, Skeletal muscle, General Medicine, DNA, Molecular biology, Mitochondria, Muscle, medicine.anatomical_structure, Biochemistry, biology.protein, Female
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fd3c792bbf362766c38b9cea0a58f35
https://pubmed.ncbi.nlm.nih.gov/12140182 -
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المؤلفون: Kerstin Hallmann, Ortrud K. Steinlein, Uwe Runge, Johannes Rebstock, Armin Heils, Colette Kananura, Wenli Gu, Karsten Haug, Thomas Sander
المصدر: Archives of neurology. 59(7)
مصطلحات موضوعية: Male, Adolescent, Genotype, Population, Mutation, Missense, Biology, Seizures, Febrile, Idiopathic generalized epilepsy, Epilepsy, Childhood absence epilepsy, Arts and Humanities (miscellaneous), medicine, Missense mutation, Humans, education, Alleles, Genetics, education.field_of_study, Splice site mutation, Polymorphism, Genetic, Reverse Transcriptase Polymerase Chain Reaction, Point mutation, Exons, medicine.disease, Receptors, GABA-A, Epilepsy, Absence, Epilepsy syndromes, Female, Neurology (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdab9c8188b5a89fceb159f44bb194e9
https://pubmed.ncbi.nlm.nih.gov/12117362 -
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المؤلفون: Joern S. Dullinger, Karsten Haug, Sabine Muth, Johannes Rebstock, Armin Heils, Christian E. Elger, Birgit Rau, Fritz Haverkamp, Peter Propping, Heike Pfeiffer, Kerstin Hallmann
المصدر: Epilepsy research. 47(3)
مصطلحات موضوعية: Male, medicine.medical_specialty, Mutation, Missense, Nerve Tissue Proteins, Immunoglobulin E, medicine.disease_cause, Sodium Channels, Idiopathic generalized epilepsy, Epilepsy, Gene Frequency, Reference Values, Internal medicine, Genetic variation, medicine, Humans, Allele frequency, Gene, Alleles, Mutation, NAV1.2 Voltage-Gated Sodium Channel, Polymorphism, Genetic, biology, Sodium channel, Genetic Variation, medicine.disease, Pedigree, Endocrinology, Neurology, Amino Acid Substitution, Immunology, biology.protein, Epilepsy, Generalized, Female, Neurology (clinical)
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المؤلفون: Anja Schwarz, Fritz Diekmann, Rüdiger Zart, Johannes Rebstock, Christian Bauer, Ines George, Hans-H. Neumayer, Berthold Hocher, Christa Thöne-Reineke
المصدر: Journal of hypertension. 18(12)
مصطلحات موضوعية: Endothelin Receptor Antagonists, Male, medicine.medical_specialty, Hypertension, Renal, Physiology, education, Ischemia, Kidney, Plasma renin activity, Peptides, Cyclic, Rats, Inbred WKY, Renovascular hypertension, Fibrosis, Internal medicine, Renin, Internal Medicine, medicine, Animals, cardiovascular diseases, business.industry, Glomerulosclerosis, Organ Size, medicine.disease, Receptor, Endothelin A, Rats, surgical procedures, operative, medicine.anatomical_structure, Endocrinology, Blood pressure, Creatinine, cardiovascular system, Atrophy, Cardiology and Cardiovascular Medicine, business, Endothelin receptor, circulatory and respiratory physiology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8ff93742a14cffb7db7366cbf5e7907
https://pubmed.ncbi.nlm.nih.gov/11132605