المؤلفون: Panagopoulos I; Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway., Andersen K; Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway., Lobmaier I; Department of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway., Lund-Iversen M; Department of Pathology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.

المصدر: Genes, chromosomes & cancer [Genes Chromosomes Cancer] 2024 Aug; Vol. 63 (8), pp. e23262.

نوع المنشور: Journal Article; Case Reports

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9007329 Publication Model: Print Cited Medium: Internet ISSN: 1098-2264 (Electronic) Linking ISSN: 10452257 NLM ISO Abbreviation: Genes Chromosomes Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Angiofibroma*/genetics , Angiofibroma*/pathology , Genetic Heterogeneity* , Chromosomes, Human, Pair 13*/genetics, Humans ; Male ; DNA-Binding Proteins/genetics ; Adult ; Female ; Retinoblastoma Binding Proteins/genetics ; MicroRNAs/genetics ; Ubiquitin-Protein Ligases/genetics ; Middle Aged ; Comparative Genomic Hybridization ; Chromosomes, Human, Pair 8/genetics ; Cathepsin B

المؤلفون: Arbatskiy M; Russian Clinical Research Center of Gerontology, Pirogov Russian National Research Medical University of the Ministry of Healthcare of the Russian Federation, 129226 Moscow, Russia., Balandin D; Russian Clinical Research Center of Gerontology, Pirogov Russian National Research Medical University of the Ministry of Healthcare of the Russian Federation, 129226 Moscow, Russia., Churov A; Russian Clinical Research Center of Gerontology, Pirogov Russian National Research Medical University of the Ministry of Healthcare of the Russian Federation, 129226 Moscow, Russia., Varachev V; Engelhardt Institute of Molecular Biology, The Russian Academy of Sciences, 119991 Moscow, Russia., Nikolaeva E; N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 115522 Moscow, Russia., Mitrofanov A; N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 115522 Moscow, Russia., Bekyashev A; N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 115522 Moscow, Russia., Tkacheva O; Russian Clinical Research Center of Gerontology, Pirogov Russian National Research Medical University of the Ministry of Healthcare of the Russian Federation, 129226 Moscow, Russia., Susova O; N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, 115522 Moscow, Russia., Nasedkina T; Engelhardt Institute of Molecular Biology, The Russian Academy of Sciences, 119991 Moscow, Russia.

المصدر: International journal of molecular sciences [Int J Mol Sci] 2024 Aug 02; Vol. 25 (15). Date of Electronic Publication: 2024 Aug 02.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Glioblastoma*/genetics , Glioblastoma*/pathology , Single-Cell Analysis*/methods , Genetic Heterogeneity* , DNA Copy Number Variations* , Brain Neoplasms*/genetics , Brain Neoplasms*/pathology, Humans ; Cell Line, Tumor ; Mutation ; Sequence Analysis, RNA/methods ; Tumor Microenvironment/genetics

المؤلفون: Yasin M; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology, Kohat, Khyber Pakhtunkhwa, 26000, Pakistan., Licchetta L; RCCS, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy., Khan N; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology, Kohat, Khyber Pakhtunkhwa, 26000, Pakistan., Ullah I; Department of Neurology, Khyber Teaching Hospital, Peshawar, Khyber Pakhtunkhwa, 25000, Pakistan., Jan Z; Department of Neurology, Pakistan Institute of Medical Science, Islamabad, 44000, Pakistan., Dawood M; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology, Kohat, Khyber Pakhtunkhwa, 26000, Pakistan., Ahmed AN; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology, Kohat, Khyber Pakhtunkhwa, 26000, Pakistan., Azeem A; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology, Kohat, Khyber Pakhtunkhwa, 26000, Pakistan., Minardi R; RCCS, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy., Carelli V; RCCS, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy. valerio.carelli@unibo.it.; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy. valerio.carelli@unibo.it., Saleha S; Department of Biotechnology and Genetic Engineering, Kohat University of Science and Technology, Kohat, Khyber Pakhtunkhwa, 26000, Pakistan. shamimsaleha@yahoo.com.

المصدر: BMC neurology [BMC Neurol] 2024 May 23; Vol. 24 (1), pp. 172. Date of Electronic Publication: 2024 May 23.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377 (Electronic) Linking ISSN: 14712377 NLM ISO Abbreviation: BMC Neurol Subsets: MEDLINE

مواضيع طبية MeSH: Epilepsy*/genetics , Epilepsy*/epidemiology , Epilepsy*/diagnosis , Comorbidity* , Genetic Heterogeneity* , Pedigree*, Humans ; Pakistan/epidemiology ; Male ; Female ; Child ; Child, Preschool ; Adolescent ; Exome Sequencing ; Adult ; Developmental Disabilities/genetics ; Developmental Disabilities/epidemiology ; Young Adult ; Intellectual Disability/genetics ; Intellectual Disability/epidemiology ; Phenotype

المؤلفون: Butnariu LI; Department of Medical Genetics, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Bizim DA; Departament of Diabetes, Saint Mary's Emergency Children Hospital, 700309 Iasi, Romania., Păduraru G; Department of Mother and Child, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Păduraru L; Department of Mother and Child, Division Neonatology, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Moisă ȘM; Department of Mother and Child, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Popa S; Department of Medical Genetics, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Gimiga N; Department of Mother and Child, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Ghiga G; Department of Mother and Child, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Bădescu MC; Department of Internal Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 16 University Street, 700115 Iasi, Romania., Lupu A; Department of Mother and Child, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania., Vasiliu I; Department of Morphofunctional Sciences II, Grigore T. Popa University of Medicine and Pharmacy, 700115 Iasi, Romania., Trandafir LM; Department of Mother and Child, Faculty of Medicine, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania.

المصدر: International journal of molecular sciences [Int J Mol Sci] 2024 May 19; Vol. 25 (10). Date of Electronic Publication: 2024 May 19.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Congenital Hyperinsulinism*/genetics , Sulfonylurea Receptors*/genetics , Genetic Heterogeneity* , Mutation* , Hypoglycemia*/genetics , Phenotype*, Humans ; Female ; Infant, Newborn ; Male ; Infant ; Potassium Channels, Inwardly Rectifying/genetics

المؤلفون: Ramzan M; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA., Zafeer MF; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA., Abad C; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA., Guo S; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA., Owrang D; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.; Institute for Auditory Neuroscience and Inner Ear Lab, University Medical Center Göttingen, Göttingen, Germany., Alper O; Department of Medical Genetics, Antalya University Medical School, Antalya, Turkey., Mutlu A; Departmet of Otolaryngology, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.; Otorhinolaryngology Clinic of Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Istanbul, Turkey., Atik T; Division of Pediatric Genetics, Ege University School of Medicine, Izmir, Turkey., Duman D; Department of Audiology, Ankara University Faculty of Health Sciences, Ankara, Turkey., Bademci G; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA., Vona B; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.; Institute for Auditory Neuroscience and Inner Ear Lab, University Medical Center Göttingen, Göttingen, Germany., Kalcioglu MT; Departmet of Otolaryngology, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.; Otorhinolaryngology Clinic of Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Istanbul, Turkey., Walz K; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.; Dr. John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA.; IQUIBICEN CONICET, Faculty of Exact and Natural Sciences, University of Buenos Aires, Buenos Aires, Argentina., Tekin M; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA. mtekin@med.miami.edu.; Dr. John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA. mtekin@med.miami.edu.

المصدر: European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Jun; Vol. 32 (6), pp. 639-646. Date of Electronic Publication: 2024 Feb 19.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Heterogeneity* , Pedigree*, Adult ; Female ; Humans ; Male ; Hearing Loss, Sensorineural/genetics ; Hearing Loss, Sensorineural/pathology ; Mutation ; Microtubule-Associated Proteins/genetics ; Microtubule-Associated Proteins/metabolism

المؤلفون: Lucas CG; Department of Pathology, Johns Hopkins University, Baltimore, MD, USA.; Department of Neurosurgery, Johns Hopkins University, Baltimore, MD, USA.; Department of Oncology, Johns Hopkins University, Baltimore, MD, USA., Mirchia K; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Seo K; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Najem H; Department of Neurological Surgery, Northwestern University, Chicago, IL, USA., Chen WC; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Zakimi N; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Foster K; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Eaton CD; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Cady MA; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Choudhury A; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Liu SJ; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Phillips JJ; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Magill ST; Department of Neurological Surgery, Northwestern University, Chicago, IL, USA., Horbinski CM; Department of Neurological Surgery, Northwestern University, Chicago, IL, USA.; Department of Pathology, Northwestern University, Chicago, IL, USA., Solomon DA; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Perry A; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA., Vasudevan HN; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA., Heimberger AB; Department of Neurological Surgery, Northwestern University, Chicago, IL, USA., Raleigh DR; Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, USA. david.raleigh@ucsf.edu.; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA. david.raleigh@ucsf.edu.; Department of Pathology, University of California San Francisco, San Francisco, CA, USA. david.raleigh@ucsf.edu.

المصدر: Nature genetics [Nat Genet] 2024 Jun; Vol. 56 (6), pp. 1121-1133. Date of Electronic Publication: 2024 May 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

مواضيع طبية MeSH: Meningioma*/genetics , Meningioma*/pathology , Meningeal Neoplasms*/genetics , Meningeal Neoplasms*/pathology , Genetic Heterogeneity*, Humans ; DNA Copy Number Variations ; Gene Expression Regulation, Neoplastic ; Genomics/methods ; Single-Cell Analysis ; Cell Proliferation/genetics ; Neoplasm Recurrence, Local/genetics ; Signal Transduction/genetics ; Cell Line, Tumor ; Transcriptome

المؤلفون: Hynds RE; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK. rob.hynds@ucl.ac.uk.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK. rob.hynds@ucl.ac.uk.; Epithelial Cell Biology in ENT Research Group (EpiCENTR), Developmental Biology and Cancer, Great Ormond Street University College London Institute of Child Health, London, UK. rob.hynds@ucl.ac.uk., Huebner A; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK.; Cancer Genome Evolution Research Group, Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK., Pearce DR; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Hill MS; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Akarca AU; Department of Cellular Pathology, University College London Hospitals, London, UK., Moore DA; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK.; Department of Cellular Pathology, University College London Hospitals, London, UK., Ward S; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK.; Advanced Sequencing Facility, The Francis Crick Institute, London, UK., Gowers KHC; Lungs for Living Research Centre, UCL Respiratory, University College London, London, UK., Karasaki T; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK.; Cancer Metastasis Laboratory, University College London Cancer Institute, London, UK., Al Bakir M; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Wilson GA; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Pich O; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Martínez-Ruiz C; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Genome Evolution Research Group, Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK., Hossain ASMM; Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, UK.; Cancer Research UK Lung Cancer Centre of Excellence, University of Manchester, Manchester, UK., Pearce SP; Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, UK.; Cancer Research UK Lung Cancer Centre of Excellence, University of Manchester, Manchester, UK., Sivakumar M; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Department of Cellular Pathology, University College London Hospitals, London, UK., Ben Aissa A; Cancer Immunology Unit, Research Department of Haematology, University College London Cancer Institute, London, UK., Grönroos E; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Chandrasekharan D; Lungs for Living Research Centre, UCL Respiratory, University College London, London, UK., Kolluri KK; Lungs for Living Research Centre, UCL Respiratory, University College London, London, UK., Towns R; Biological Services Unit, University College London, London, UK., Wang K; School of Medicine, University of Leeds, Leeds, UK., Cook DE; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Bosshard-Carter L; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Lungs for Living Research Centre, UCL Respiratory, University College London, London, UK., Naceur-Lombardelli C; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK., Rowan AJ; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK., Veeriah S; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK., Litchfield K; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Tumour Immunogenomics and Immunosurveillance Laboratory, University College London Cancer Institute, London, UK., Crosbie PAJ; Cancer Research UK Lung Cancer Centre of Excellence, University of Manchester, Manchester, UK.; Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, UK., Dive C; Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, UK.; Cancer Research UK Lung Cancer Centre of Excellence, University of Manchester, Manchester, UK., Quezada SA; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Immunology Unit, Research Department of Haematology, University College London Cancer Institute, London, UK., Janes SM; Lungs for Living Research Centre, UCL Respiratory, University College London, London, UK., Jamal-Hanjani M; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.; Cancer Metastasis Laboratory, University College London Cancer Institute, London, UK.; Department of Oncology, University College London Hospitals, London, UK., Marafioti T; Department of Cellular Pathology, University College London Hospitals, London, UK., McGranahan N; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK. nicholas.mcgranahan.10@ucl.ac.uk.; Cancer Genome Evolution Research Group, Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK. nicholas.mcgranahan.10@ucl.ac.uk., Swanton C; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK. charles.swanton@crick.ac.uk.; Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK. charles.swanton@crick.ac.uk.; Department of Oncology, University College London Hospitals, London, UK. charles.swanton@crick.ac.uk.

مؤلفون مشاركون: TRACERx consortium

المصدر: Nature communications [Nat Commun] 2024 May 31; Vol. 15 (1), pp. 4653. Date of Electronic Publication: 2024 May 31.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

مواضيع طبية MeSH: Carcinoma, Non-Small-Cell Lung*/genetics , Carcinoma, Non-Small-Cell Lung*/pathology , Lung Neoplasms*/genetics , Lung Neoplasms*/pathology , Mice, Inbred NOD* , Mice, SCID* , Genetic Heterogeneity*, Humans ; Animals ; Mice ; Female ; Exome Sequencing ; Genomics/methods ; Male ; Xenograft Model Antitumor Assays ; Heterografts ; Disease Models, Animal ; Aged ; Middle Aged

المؤلفون: Langerud J; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway., Eilertsen IA; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway., Moosavi SH; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway., Klokkerud SMK; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway., Reims HM; Department of Pathology, Oslo University Hospital, Oslo, Norway., Backe IF; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.; Department of Gastrointestinal Surgery, Oslo University Hospital, Oslo, Norway., Hektoen M; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway., Sjo OH; Department of Gastrointestinal Surgery, Oslo University Hospital, Oslo, Norway., Jeanmougin M; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway., Tejpar S; Molecular Digestive Oncology, Department of Oncology, Katholieke Universiteit Leuven, Leuven, Belgium., Nesbakken A; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.; Department of Gastrointestinal Surgery, Oslo University Hospital, Oslo, Norway., Lothe RA; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway., Sveen A; Department of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway. anita.sveen@rr-research.no.; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway. anita.sveen@rr-research.no.

المصدر: Nature communications [Nat Commun] 2024 May 21; Vol. 15 (1), pp. 4342. Date of Electronic Publication: 2024 May 21.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms*/genetics , Colorectal Neoplasms*/pathology , Colorectal Neoplasms*/mortality , Colorectal Neoplasms*/classification , Transcriptome* , Genetic Heterogeneity* , Tumor Microenvironment*/genetics , Gene Expression Regulation, Neoplastic*, Humans ; Prognosis ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Gene Expression Profiling/methods ; Female ; Male ; Single-Cell Analysis/methods ; Aged ; Middle Aged

المؤلفون: Beigi YZ; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran., Lanjanian H; Software Engineering Department, Engineering Faculty, Istanbul Topkapi University, Istanbul, Turkey., Fayazi R; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran., Salimi M; Department of Medical Genetics, Institute of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran., Hoseyni BHM; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran., Noroozizadeh MH; Negah Eye Hospital, Tehran, Iran., Masoudi-Nejad A; Laboratory of System Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran. amasoudin@ut.ac.ir.

المصدر: Molecular biomedicine [Mol Biomed] 2024 May 10; Vol. 5 (1), pp. 17. Date of Electronic Publication: 2024 May 10.

نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Springer Singapore Country of Publication: Singapore NLM ID: 9918283581406676 Publication Model: Electronic Cited Medium: Internet ISSN: 2662-8651 (Electronic) Linking ISSN: 26628651 NLM ISO Abbreviation: Mol Biomed Subsets: MEDLINE

مواضيع طبية MeSH: Melanoma*/genetics , Melanoma*/pathology , Melanoma*/therapy , Melanoma*/drug therapy , Molecular Targeted Therapy*/methods , Genetic Heterogeneity* , Uveal Neoplasms*/genetics , Uveal Neoplasms*/therapy , Uveal Neoplasms*/pathology, Humans ; Neoplastic Cells, Circulating/metabolism ; Neoplastic Cells, Circulating/pathology ; Biomarkers, Tumor/genetics ; Mutation ; Circulating Tumor DNA/genetics ; Circulating Tumor DNA/blood ; Liquid Biopsy/methods

المؤلفون: Arfan S; Division of Molecular Pathology, The Institute of Cancer Research, 15 Cotswold Road, Sutton, SM2 5NG, UK., Thway K; Division of Molecular Pathology, The Institute of Cancer Research, 15 Cotswold Road, Sutton, SM2 5NG, UK.; The Royal Marsden NHS Foundation Trust, Fulham Road, London, SW3 6JJ, UK., Jones RL; The Royal Marsden NHS Foundation Trust, Fulham Road, London, SW3 6JJ, UK.; Division of Clinical Studies, The Institute of Cancer Research, 15 Cotswold Road, Sutton, SM2 5NG, UK., Huang PH; Division of Molecular Pathology, The Institute of Cancer Research, 15 Cotswold Road, Sutton, SM2 5NG, UK. paul.huang@icr.ac.uk.

المصدر: Current treatment options in oncology [Curr Treat Options Oncol] 2024 May; Vol. 25 (5), pp. 644-658. Date of Electronic Publication: 2024 Apr 24.

نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Current Science, Inc Country of Publication: United States NLM ID: 100900946 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1534-6277 (Electronic) Linking ISSN: 15346277 NLM ISO Abbreviation: Curr Treat Options Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Leiomyosarcoma*/genetics , Leiomyosarcoma*/therapy , Leiomyosarcoma*/diagnosis , Leiomyosarcoma*/pathology , Leiomyosarcoma*/mortality , Precision Medicine*/methods , Genetic Heterogeneity* , Biomarkers, Tumor*, Humans ; Prognosis ; Disease Management ; Disease Susceptibility ; Molecular Targeted Therapy