المؤلفون: Maria I. Kontaridis, Amy E. Roberts, Lisa Schill, Lisa Schoyer, Beth Stronach, Gregor Andelfinger, Yoko Aoki, Marni E. Axelrad, Annette Bakker, Anton M. Bennett, Alberto Broniscer, Pau Castel, Caitlin A. Chang, Lukas Cyganek, Tirtha K. Das, Jeroen Hertog, Emilia Galperin, Shruti Garg, Bruce D. Gelb, Kristiana Gordon, Tamar Green, Karen W. Gripp, Maxim Itkin, Maija Kiuru, Bruce R. Korf, Jeff R. Livingstone, Alejandro López‐Juárez, Pilar L. Magoulas, Sahar Mansour, Theresa Milner, Elisabeth Parker, Elizabeth I. Pierpont, Kevin Plouffe, Katherine A. Rauen, Suma P. Shankar, Shane B. Smith, David A. Stevenson, Marco Tartaglia, Richard Van, Morgan E. Wagner, Stephanie M. Ware, Martin Zenker

المساهمون: Hubrecht Institute for Developmental Biology and Stem Cell Research

المصدر: American journal of medical genetics. Part A, vol 188, iss 6
Kontaridis, M I, Roberts, A E, Schill, L, Schoyer, L, Stronach, B, Andelfinger, G, Aoki, Y, Axelrad, M E, Bakker, A, Bennett, A M, Broniscer, A, Castel, P, Chang, C A, Cyganek, L, Das, T K, den Hertog, J, Galperin, E, Garg, S, Gelb, B D, Gordon, K, Green, T, Gripp, K W, Itkin, M, Kiuru, M, Korf, B R, Livingstone, J R, López-Juárez, A, Magoulas, P L, Mansour, S, Milner, T, Parker, E, Pierpont, E I, Plouffe, K, Rauen, K A, Shankar, S P, Smith, S B, Stevenson, D A, Tartaglia, M, Van, R, Wagner, M E, Ware, S M & Zenker, M 2022, ' The seventh international RASopathies symposium : Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discovery ', American Journal of Medical Genetics. Part A . https://doi.org/10.1002/ajmg.a.62716
American Journal of Medical Genetics, Part A, 188(6), 1915-1927. Wiley-Liss Inc.

مصطلحات موضوعية: Pediatric, neurofibromatosis, ras Proteins/genetics, Noonan Syndrome, Costello Syndrome, Clinical Sciences, cardiofaciocutaneus syndrome, Costello Syndrome/genetics, RASopathy, Good Health and Well Being, Noonan Syndrome/genetics, ras Proteins, Genetics, Humans, 2.1 Biological and endogenous factors, Mitogen-Activated Protein Kinases, Aetiology, Mitogen-Activated Protein Kinases/metabolism, signaling, Genetics (clinical), Signal Transduction

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66770a599b697c0d77d007bd425f8e74
https://escholarship.org/uc/item/44s997fh

المؤلفون: Marialetizia Motta, Maja Solman, Adeline A Bonnard, Alma Kuechler, Francesca Pantaleoni, Manuela Priolo, Balasubramanian Chandramouli, Simona Coppola, Simone Pizzi, Erika Zara, Marco Ferilli, Hülya Kayserili, Roberta Onesimo, Chiara Leoni, Julia Brinkmann, Yoann Vial, Susanne B Kamphausen, Cécile Thomas-Teinturier, Anne Guimier, Viviana Cordeddu, Laura Mazzanti, Giuseppe Zampino, Giovanni Chillemi, Martin Zenker, Hélène Cavé, Jeroen den Hertog, Marco Tartaglia

المساهمون: Hubrecht Institute for Developmental Biology and Stem Cell Research, Karabey, Hülya Kayserili (ORCID 0000-0003-0376-499X & YÖK ID 7945), Motta, Marialetizia, Solman, Maja, Bonnard, Adeline, Kuechler, Alma, Pantaleoni, Francesca, Priolo, Manuela, Chandramouli, Balasubramanian, Coppola, Simona, Pizzi, Simone, Zara, Erika, Ferilli, Marco, Onesimo, Roberta, Leoni, Chiara, Brinkmann, Julia, Vial, Yoann, Kamphausen, Susanne B., Thomas-Teinturier, Cecile, Guimier, Anne, Cordeddu, Viviana, Mazzanti, Laura, Zampino, Giuseppe, Chillemi, Giovanni, Zenker, Martin, Cave, Helene, Hertog, Jeroen, Tartaglia, Marco, Koç University Hospital, School of Medicine

المصدر: Human Molecular Genetics, 31(16), 2766-2778. Oxford University Press
Human Molecular Genetics

مصطلحات موضوعية: ras Proteins/genetics, Medizin, Loose Anagen Hair Syndrome/genetics, functional validation, Biochemistry and molecular biology, Genetics and heredity, RAS signalling, Abnormalities, Multiple/genetics, Loose Anagen Hair Syndrome, Genetics, Humans, Noonan syndrome, Abnormalities, Multiple, Molecular Biology, Genetics (clinical), SHOC2, Intracellular Signaling Peptides and Proteins, General Medicine, MAPK, SHOC2, Noonan syndrome, RASopathy, MAPK, RAS signalling, functional validation, Phenotype, RASopathy, Multiple/genetics, ras Proteins, Abnormalities, Phenotypecongenital abnormality, Signal transduction, Cell membrane, Embryo, Growth factor, Leucine, Mitogen-activated protein kinases, Protein kinase, Up-regulation (physiology) zebrafish genetics, Homogeneity, Fluid flow, Functional behavior, Psychology, Intracellular Signaling Peptides and Proteins/genetics

وصف الملف: pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4274a128c94c54387070cf691ea74309
https://hdl.handle.net/11573/1620615

المؤلفون: Rosanna Pescini-Gobert, Beryl Royer-Bertrand, Ikram El Zaoui, Leonidas Zografos, Serge Leyvraz, Nicolo Riggi, Carlo Rivolta, Alexandre Moulin, Marc Folcher, Michael Nicolas, Katarina Cisarova, Virginie G. Peter, Donata Rimoldi, Ann Schalenbourg

المصدر: PLoS Genetics, Vol 16, Iss 12, p e1009201 (2020)
PLoS Genetics
PLoS genetics, vol. 16, no. 12, pp. e1009201

مصطلحات موضوعية: Male, Cancer Research, Skin Neoplasms, Somatic cell, Gene Expression, QH426-470, medicine.disease_cause, Cell Line, Tumor, Conjunctival Neoplasms/genetics, Conjunctival Neoplasms/metabolism, DNA Copy Number Variations, Female, Humans, Melanoma/genetics, Melanoma/metabolism, Middle Aged, Mutation, Neurofibromin 1/genetics, Proto-Oncogene Proteins B-raf/genetics, Transcriptome, ras Proteins/genetics, 0302 clinical medicine, Basic Cancer Research, Medicine and Health Sciences, Skin Tumors, Melanoma, Genetics (clinical), 0303 health sciences, Neurofibromin 1, Genomics, Oncology, 030220 oncology & carcinogenesis, Cutaneous Melanoma, Transcriptome Analysis, Research Article, Proto-Oncogene Proteins B-raf, Malignant Skin Neoplasms, Conjunctival Neoplasms, Dermatology, Biology, 03 medical and health sciences, Germline mutation, Malignant Tumors, Cancer Genomics, Genomic Medicine, medicine, Genetics, Molecular Biology, Gene, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Cancers and Neoplasms, Biology and Life Sciences, Computational Biology, Genome Analysis, Cutaneous melanoma, Cancer research, ras Proteins, Somatic Mutation, Carcinogenesis, Conjunctival Melanoma

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9a3eb0b18a9b07247281064ff06625a
https://doaj.org/article/6d13f01c6aab43f98a7237adb4d4366b

المؤلفون: Christoph Geissler, Wolfgang R. Sperr, Armin Zebisch, Michael Gurbisz, Michael Pfeilstöcker, Ulrich Germing, Gregor Hörmann, Ernst Ulsperger, Temeida Graf, Rajko Kusec, Felix Keil, Elmir Graf, Reinhard Stauder, Eva Jäger, Otto Zach, Leopold Öhler, Klaus Geissler, Sonja Heibl, Josef Thaler, Peter Bettelheim, Heinz Tüchler, Bruno Schneeweiss, Ansgar Weltermann, Peter Valent, Paul Knöbl, Agnes Barna, Thomas Nösslinger, Thamer Sliwa, Ilse Schwarzinger, Ulrich Jäger, Heinz Sill, Sigrid Machherndl-Spandl

المصدر: International Journal of Molecular Sciences
Volume 21
Issue 8
International Journal of Molecular Sciences, Vol 21, Iss 3025, p 3025 (2020)

مصطلحات موضوعية: 0301 basic medicine, Myeloid, Leukemia, Myelomonocytic, Chronic / metabolism, Leukemia, Myelomonocytic, Chronic / mortality, Gene mutation, medicine.disease_cause, Leukemia, Myelomonocytic, Chronic / genetics, lcsh:Chemistry, Pathogenesis, 0302 clinical medicine, AML, hemic and lymphatic diseases, ras Proteins / metabolism, lcsh:QH301-705.5, Spectroscopy, Mutation, Gene Expression Regulation, Leukemic, CFU-GM, Myeloid leukemia, Leukemia, Myelomonocytic, Chronic, General Medicine, Prognosis, Computer Science Applications, Cell Transformation, Neoplastic / genetics, RAS-pathway mutations, medicine.anatomical_structure, Cell Transformation, Neoplastic, 030220 oncology & carcinogenesis, Cytogenetic Analysis, Disease Progression, Neoplastic Stem Cells, Signal Transduction, Neoplastic Stem Cells / metabolism, Chronic myelomonocytic leukemia, RASopathy, Catalysis, Article, Inorganic Chemistry, 03 medical and health sciences, Leukemia, Myelomonocytic, Chronic / pathology, medicine, Humans, Physical and Theoretical Chemistry, Molecular Biology, Neoplasm Staging, Retrospective Studies, CMML, business.industry, Organic Chemistry, Cell Transformation, Neoplastic / metabolism, medicine.disease, ras Proteins / genetics, 030104 developmental biology, lcsh:Biology (General), lcsh:QD1-999, Cancer research, ras Proteins, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12b7d789465abdf30a6bbc14a9ea7c88
http://europepmc.org/articles/PMC7215883

المؤلفون: Klaus Pantel, Zahra Eslami-S, Luis Enrique Cortés-Hernández, Catherine Alix-Panabières

المساهمون: Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Universitaetsklinikum Hamburg-Eppendorf = University Medical Center Hamburg-Eppendorf [Hamburg] (UKE)

المصدر: Clinical Chemistry
Clinical Chemistry, American Association for Clinical Chemistry, 2020, 66 (1), pp.97-104. ⟨10.1373/clinchem.2019.303586⟩

مصطلحات موضوعية: 0301 basic medicine, Proto-Oncogene Proteins B-raf, Proteome, MESH: Proto-Oncogene Proteins B-raf / genetics, Receptor, ErbB-2 / genetics, Receptor, ErbB-2 / metabolism, Transcriptome, ras Proteins / genetics, Receptor, ErbB-2, Clinical Biochemistry, Programmed Cell Death 1 Receptor, MESH: Biomarkers, Tumor / genetics, Biomarkers, Tumor / metabolism, Humans, Liquid Biopsy, Neoplastic Cells, Circulating / metabolism, [SDV.CAN]Life Sciences [q-bio]/Cancer, Computational biology, Metastasis, 03 medical and health sciences, 0302 clinical medicine, Circulating tumor cell, Clinical information, medicine, Biomarkers, Tumor, Functional studies, Liquid biopsy, business.industry, Biochemistry (medical), Cancer, medicine.disease, Neoplastic Cells, Circulating, 3. Good health, MESH: Neoplastic Cells, Circulating / pathology, Programmed Cell Death 1 Receptor / genetics, Programmed Cell Death 1 Receptor / metabolism, Proteome / metabolism, 030104 developmental biology, 030220 oncology & carcinogenesis, Tissue biopsies, ras Proteins, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b512907555df9d84e9a4ee41ea857ae
https://hal.umontpellier.fr/hal-02529297

المؤلفون: David A. Hinds, Bjarke Feenstra, Bo Jacobsson, Nadia K. Litterman, Mika Rämet, Kelli K Ryckman, Lisa M. Muglia, Youna Hu, Jamie Maziarz, Minna K. Karjalainen, Leah C. Kottyan, Carmy Forney, Mauris C. Nnamani, Daniel Miller, Johanna M. Huusko, Matthew T. Weirauch, Ellen A. Nohr, Allison Momany, George Davey Smith, Frank Geller, Xueping Liu, Bruce Bedell, Aarno Palotie, Mihaela Pavlicev, Arun R. Chavan, Louis J. Muglia, Pan Pan Jiang, Kari Teramo, Heather A. Boyd, Mads Melbye, Mikko Hallman, Verena Sengpiel, Günter P. Wagner, Julius Juodakis, Xiaoting Chen, Jonas Bacelis, Ge Zhang, Laura Russell

المساهمون: Institute for Molecular Medicine Finland, Aarno Palotie / Principal Investigator, University of Helsinki, HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, Genomics of Neurological and Neuropsychiatric Disorders, Lääketieteen ja biotieteiden tiedekunta - Faculty of Medicine and Life Sciences, Tampere University

المصدر: Zhang, G, Feenstra, B, Bacelis, J, Liu, X, Muglia, L M, Juodakis, J, Miller, D E, Litterman, N, Jiang, P-P, Russell, L, Hinds, D A, Hu, Y, Weirauch, M T, Chen, X, Chavan, A R, Wagner, G P, Pavličev, M, Nnamani, M C, Maziarz, J, Karjalainen, M K, Rämet, M, Sengpiel, V, Geller, F, Boyd, H A, Palotie, A, Momany, A, Bedell, B, Ryckman, K K, Huusko, J M, Forney, C R, Kottyan, L C, Hallman, M, Teramo, K, Nohr, E A, Davey Smith, G, Melbye, M, Jacobsson, B & Muglia, L J 2017, ' Genetic Associations with Gestational Duration and Spontaneous Preterm Birth ', The New England Journal of Medicine, vol. 377, no. 12, pp. 1156-1167 . https://doi.org/10.1056/NEJMoa1612665
Zhang, G, Feenstra, B, Bacelis, J, Liu, X, Muglia, L M, Juodakis, J, Litterman, N, Hinds, D A, Hu, Y, Weirauch, M T, Chen, X, Chavan, A R, Wagner, G P, Pavličev, M, Nnamani, M C, Maziarz, J, Karjalainen, M K, Rämet, M, Sengpiel, V, Geller, F, Boyd, H A, Palotie, A, Momany, A, Bedell, B, Ryckman, K K, Huusko, J M, Forney, C R, Kottyan, L C, Hallman, M, Teramo, K, Nohr, E A, Smith, G D, Melbye, M, Jacobsson, B & Muglia, L J 2017, ' Genetic associations with gestational duration and spontaneous preterm birth ', New England Journal of Medicine, vol. 377, no. 12, pp. 1156-1167 . https://doi.org/10.1056/NEJMoa1612665
The New England Journal of Medicine
Zhang, G, Feenstra, B, Bacelis, J, Liu, X, Muglia, L M, Juodakis, J, Miller, D E, Litterman, N, Jiang, P P, Russell, L, Hinds, D A, Hu, Y, Weirauch, M T, Chen, X, Chavan, A R, Wagner, G P, Pavličev, M, Nnamani, M C, Maziarz, J, Karjalainen, M K, Ramet, M, Sengpiel, V, Geller, F, Boyd, H A, Palotie, A, Momany, A, Bedell, B, Ryckman, K K, Huusko, J M, Forney, C R, Kottyan, L C, Hallman, M, Teramo, K, Nohr, E A, Davey Smith, G, Melbye, M, Jacobsson, B & Muglia, L J 2018, ' Genetic Associations with Gestational Duration and Spontaneous Preterm Birth ', Obstetrical and Gynecological Survey, vol. 73, no. 2, pp. 83-85 . https://doi.org/10.1097/01.ogx.0000530434.15441.45

مصطلحات موضوعية: 0301 basic medicine, ras Proteins/genetics, LOCI, Datasets as Topic, Physiology, Genome-wide association study, VARIANTS, SUSCEPTIBILITY, Bioinformatics, 0302 clinical medicine, Polymorphism (computer science), single nucleotide polymorphism, 3123 Gynaecology and paediatrics, Wnt4 Protein, Pregnancy, 030202 anesthesiology, Medicine, RISK, 030219 obstetrics & reproductive medicine, Obstetrics, Receptor, Angiotensin, Type 2/genetics, Gestational age, Obstetrics and Gynecology, Naisten- ja lastentaudit - Gynaecology and paediatrics, General Medicine, Adenylyl Cyclases/genetics, DIFFERENTIATION, Phenotype, Duration (music), Premature Birth, Regression Analysis, Gestation, Female, Research Article, Adenylyl Cyclases, medicine.medical_specialty, Biolääketieteet - Biomedicine, Gestational Age, Receptor, Angiotensin, Type 2, Polymorphism, Single Nucleotide, Trans-Activators/genetics, 03 medical and health sciences, AGE, genomewide association, Genetiikka, kehitysbiologia, fysiologia - Genetics, developmental biology, physiology, Genetic variation, Humans, Genetic Predisposition to Disease, Continuous trait, GENOME-WIDE ASSOCIATION, POLYMORPHISMS, business.industry, ENDOMETRIOSIS, Genetic variants, preterm birth, Genetic Variation, Gestational length, Premature Birth/genetics, medicine.disease, Peptide Elongation Factors, 030104 developmental biology, 3121 General medicine, internal medicine and other clinical medicine, Peptide Elongation Factors/genetics, Genomewide association, Trans-Activators, ras Proteins, WEIGHT, 3111 Biomedicine, Wnt4 Protein/genetics, business, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf; fulltext

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49c91222807de9a168bf9bb010ac555b
https://doi.org/10.1097/01.ogx.0000530434.15441.45

المؤلفون: Finn Larsen, Tim Svenstrup Poulsen, Jesper Andreas Palshof, Troels Dreier Christensen, Mette Karen Yilmaz, Dorte Nielsen, Per Pfeiffer, Estrid Høgdall, Benny Vittrup Jensen

المصدر: Christensen, T D, Palshof, J A, Larsen, F O, Poulsen, T S, Høgdall, E, Pfeiffer, P, Jensen, B V, Yilmaz, M K & Nielsen, D 2018, ' Associations between primary tumor RAS, BRAF and PIK3CA mutation status and metastatic site in patients with chemo-resistant metastatic colorectal cancer ', Acta Oncologica, vol. 57, no. 8, pp. 1057-1062 . https://doi.org/10.1080/0284186X.2018.1433322

مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, Peritoneal Neoplasms/genetics, Lung Neoplasms, Skin Neoplasms, Colorectal cancer, ras Proteins/genetics, Drug Resistance, Neoplasm/drug effects, 0302 clinical medicine, Peritoneal Neoplasms, Ovarian Neoplasms, Aged, 80 and over, Colorectal Neoplasms/drug therapy, Hematology, General Medicine, Middle Aged, Primary tumor, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Female, Colorectal Neoplasms, Proto-Oncogene Proteins B-raf, Adult, medicine.medical_specialty, Lung Neoplasms/genetics, Class I Phosphatidylinositol 3-Kinases, macromolecular substances, 03 medical and health sciences, Ovarian Neoplasms/genetics, Text mining, Internal medicine, Skin Neoplasms/genetics, Proto-Oncogene Proteins B-raf/genetics, medicine, Humans, Radiology, Nuclear Medicine and imaging, In patient, neoplasms, Aged, Class I Phosphatidylinositol 3-Kinases/genetics, Retrospective Studies, business.industry, Pik3ca mutation, Retrospective cohort study, medicine.disease, digestive system diseases, 030104 developmental biology, Drug Resistance, Neoplasm, Mutation, ras Proteins, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf98416f75feb7db39e632b0333431b
https://vbn.aau.dk/da/publications/66c3927a-7073-4475-a961-94abcf1b7d6a

المؤلفون: Kim M. Keppler-Noreuil, Abby Sandler, Chiara Leoni, Karlyne M. Reilly, Bronwyn Kerr, Frank McCormick, Anne Goriely, David Neal Franz, Amy E. Roberts, Scott R. Plotkin, Karen W. Gripp, Michael Fisher, Bruce R. Korf, Brigitte C. Widemann, Pinar Bayrak-Toydemir, Kathryn C. Chatfield, Annette Bakker, Karin S. Walsh, Brage S. Andresen, Emma Burkitt-Wright, Florent Elefteriou, Antonio Y. Hardan, Katherine A. Rauen, Bruce D Gelb, Dawn H. Siegel, Ype Elgersma, Lisa Schill, Lisa Schoyer, David A. Stevenson

المساهمون: Neurosciences

المصدر: Stevenson, D A, Schill, L, Schoyer, L, Andresen, B S, Bakker, A, Bayrak-Toydemir, P, Burkitt-Wright, E, Chatfield, K, Elefteriou, F, Elgersma, Y, Fischer, MJ, Franz, D, Gelb, B, Goriely, A, Gripp, KW, Hardan, A, Keppler-Noreuil, K, Kerr, B, Korf, B, Leoni, C, McCormick, F, Plotkin, S, Rauen, KA, Reilly, K, Roberts, A, Sandler, A, Siegel, D, Walsh, K & Widemann, BC 2016, ' The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway ', American Journal of Medical Genetics. Part A, vol. 170, no. 8, pp. 1959-1966 . https://doi.org/10.1002/ajmg.a.37723
American Journal of Medical Genetics Part A, 170(8), 1959-1966. Wiley-Liss Inc.
American journal of medical genetics. Part A, vol 170, iss 8

مصطلحات موضوعية: MAPK/ERK pathway, Clinical Sciences, Ras/MAPK, ras Proteins/genetics, experimental models, RASopathy, Article, Capital Financing, Congenital, 03 medical and health sciences, Rare Diseases, 0302 clinical medicine, Costello syndrome, Genetics, medicine, cancer, Humans, Family, Neurofibromatosis, rare disorders, Intersectoral Collaboration, Genetics (clinical), Pediatric, Legius syndrome, clinical trials, Clinical Trials as Topic, business.industry, Ras mapk, Neurosciences, Mitogen-Activated Protein Kinases/genetics, medicine.disease, MAPK, Inborn, Genetic Diseases, 030220 oncology & carcinogenesis, ras Proteins, Genetic Diseases, Inborn/diagnosis, Cancer research, Congenital Structural Anomalies, Noonan syndrome, Mitogen-Activated Protein Kinases, business, 030217 neurology & neurosurgery, Noonan Syndrome with Multiple Lentigines, Ras, Signal Transduction

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b081068c6333a3e219e60449b203d5f3
https://doi.org/10.1002/ajmg.a.37723

المؤلفون: Ana Pestana, Margarida Sá Fernandes, Manuel Campos, Sofia Macedo, Agostinho Sanches, Armando Baptista, João Vinagre, Joana Pardal, Rui Batista, José Manuel Lopes, Paula Soares

المساهمون: Instituto de Investigação e Inovação em Saúde

المصدر: Genes
Volume 11
Issue 7
Genes, Vol 11, Iss 751, p 751 (2020)

مصطلحات موضوعية: p53, Male, Skin Neoplasms, cutaneous squamous cell carcinoma, Carcinoma, Squamous Cell / genetics, Cell, Expression, Metastases, medicine.disease_cause, 030207 dermatology & venereal diseases, 0302 clinical medicine, Recurrence, Carcinoma, Squamous Cell / pathology, ras Proteins / metabolism, Medicine, Neoplasm Metastasis, prognostic biomarker, P53 expression, Skin Neoplasms / genetics, Genetics (clinical), Outcome, Aged, 80 and over, Univariate analysis, Mutation, ras Proteins / standards, Skin Neoplasms / metabolism, Prognosis, Tumor Suppressor Protein p53 / genetics, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Carcinoma, Squamous Cell, outcome, biomarker, Immunohistochemistry, Biomarker (medicine), Female, RAS, Carcinoma, Squamous Cell / metabolism, recurrence, Prognostic biomarker, Cutaneous squamous cell carcinoma, lcsh:QH426-470, Biomarkers, Tumor / metabolism, Article, Tumor Suppressor Protein p53 / standards, Biomarkers, Tumor / standards, 03 medical and health sciences, expression, Biomarkers, Tumor, Genetics, Humans, metastases, Gene, Aged, P53, Skin Neoplasms / pathology, Tumor Suppressor Protein p53 / metabolism, business.industry, Biomarker, ras Proteins / genetics, lcsh:Genetics, Biomarkers, Tumor / genetics, ras Proteins, Cancer research, prognosis, Tumor Suppressor Protein p53, mutation, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9774ecc8f78c665d7549c95d89ccbcd5
https://doi.org/10.3390/genes11070751

المؤلفون: Matthew P. Conomos, Sonia Ancoli-Israel, Simon C. Warby, Beate Stubbe, Phyllis C. Zee, W. Craig Johnson, Xihong Lin, Adrienne M. Stilp, Neomi A. Shah, Daniel J. Gottlieb, Thomas Penzel, Seung Ku Lee, Scott A. Sands, Richa Saxena, Chaolong Wang, Xiaofeng Zhu, Cathy C. Laurie, Zoltán Kutalik, Andrew Bjonnes, Jingjing Liang, Graeme I. Bell, D. Andrew Wellman, Raanan Arens, Susan Redline, Lyle J. Palmer, Alexander Teumer, Kevin J. Gleason, Kent D. Taylor, Emma K. Larkin, Erika W. Hagen, Gregory J. Tranah, Mehdi Tafti, George J. Papanicolaou, Kenneth Rice, Sanjay R. Patel, David R. Hillman, Craig L. Hanis, Chol Shin, Sutapa Mukherjee, Daniel S. Evans, Jerome I. Rotter, Ralf Ewert, Jennifer E. Below, Wendy S. Post, Brian E. Cade, Tamar Sofer, Sina A. Gharib, Raphael Heinzer, Jae Hoon Sul, Sung Chun, Han Chen, Alexis C. Frazier-Wood, Jacqueline M. Lane, José Haba-Rubio, Heming Wang, Timothy A. Thornton, Jose S. Loredo, Alberto R. Ramos, Ali Azarbarzin, Shamil R. Sunyaev, Katie L. Stone, Paul E. Peppard

المصدر: American journal of respiratory cell and molecular biology, vol. 58, no. 3, pp. 391-401
American journal of respiratory cell and molecular biology, vol 58, iss 3

مصطلحات موضوعية: 0301 basic medicine, Male, Phosphatidylethanolamine N-Methyltransferase, Respiratory System, Clinical Biochemistry, Prevalence, Genome-wide association study, Cardiorespiratory Medicine and Haematology, 2.1 Biological and endogenous factors, Aetiology, Lung, obstructive sleep apnea, Original Research, Genetics, Sex Characteristics, Sleep Apnea, Obstructive, Adult, Aged, Female, Genome-Wide Association Study, Humans, Middle Aged, Phosphatidylethanolamine N-Methyltransferase/genetics, Quantitative Trait Loci/genetics, Sleep Apnea, Obstructive/genetics, Sleep, REM/physiology, Sterol Regulatory Element Binding Protein 1/genetics, Transcription Factors/genetics, ras Proteins/genetics, genetics, genome-wide association studies, multiethnic, sexual dimorphism, Meta-analysis, Sleep Research, Sterol Regulatory Element Binding Protein 1, Sex characteristics, Pulmonary and Respiratory Medicine, Sleep Apnea, Quantitative Trait Loci, Sleep, REM, Biology, Quantitative trait locus, 03 medical and health sciences, Clinical Research, medicine, Molecular Biology, Genetic association, Obstructive, Human Genome, Cell Biology, medicine.disease, respiratory tract diseases, nervous system diseases, Sexual dimorphism, Obstructive sleep apnea, 030104 developmental biology, REM, Trans-Activators, ras Proteins, Sleep, Transcription Factors

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3ffcb9b8efdc75ec6d8608da58d9c65
https://europepmc.org/articles/PMC5854957/