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1دورية أكاديمية
المؤلفون: Chunni Chen, Yuxi Gong, Yefan Yang, Qiuyuan Xia, Qiu Rao, Yang Shao, Liuqing Zhu, Junli Zhang, Xiao Li, Pan Ji, Boya Zhai, Xiang Zhang, Zhihong Zhang
المصدر: Diagnostic Pathology, Vol 16, Iss 1, Pp 1-11 (2021)
مصطلحات موضوعية: Monomorphic epitheliotropic intestinal T-cell lymphoma, Whole-exome sequencing, JAK-STAT pathway, Amplification of chromosome 9q, Pathology, RB1-214
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1746-1596Test
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2دورية أكاديمية
المؤلفون: Smith, Moyra, Sperling, Donald
المصدر: American Journal of Medical Genetics. 84(4)
مصطلحات موضوعية: Genetics, Pediatric, Rare Diseases, Brain Disorders, Heart Disease, Tuberous Sclerosis, Cardiovascular, Aetiology, 2.1 Biological and endogenous factors, Base Sequence, Chromosomes, Human, Pair 16, Chromosomes, Human, Pair 9, Exons, Gene Duplication, Heart Neoplasms, Humans, Infant, Newborn, Male, Molecular Sequence Data, Polymerase Chain Reaction, Proteins, Rhabdomyoma, Tuberous Sclerosis Complex 1 Protein, Tumor Suppressor Proteins, cardiac rhabdomyoma, tuberous sclerosis, mutation analysis, TSC1, hamartin, base pair duplication, Cardiac rhabdomyoma, Hamartin, Mutation analysis, Tuberous sclerosis, DNA, article, base pairing, case report, chromosome 16p, chromosome 9q, crossing over, DNA sequence, exon, gene duplication, gene mutation, heart tumor, human, hypomelanosis, infant, priority journal, rhabdomyoma, Clinical Sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/50d208chTest
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3دورية أكاديمية
المؤلفون: Green, Andrew J, Smith, Moyra, Yates, John RW
المصدر: Nature Genetics. 6(2)
مصطلحات موضوعية: Biological Sciences, Genetics, Brain Disorders, Rare Diseases, Neurosciences, Tuberous Sclerosis, Aetiology, 2.1 Biological and endogenous factors, Alleles, Angiomyolipoma, Astrocytoma, Chromosomes, Human, Pair 16, Chromosomes, Human, Pair 9, DNA, Neoplasm, Female, Gene Deletion, Genes, Tumor Suppressor, Genetic Markers, Hamartoma, Heterozygote, Humans, Kidney Neoplasms, Male, Pedigree, dna marker, tumor marker, angiomyolipoma, article, astrocytoma, autosomal dominant disorder, chromosome 16p, chromosome 9q, gene mapping, genetic linkage, hamartoma, heterozygosity, human, polymerase chain reaction, priority journal, rhabdomyoma, tuberous sclerosis, tumor suppressor gene, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/5gx0c96qTest
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4دورية أكاديمية
المؤلفون: POVEY, S, SMITH, M, HAINES, J, KWIATKOWSKI, D, FOUNTAIN, J, BALE, A, ABBOTT, C, JACKSON, I, LAWRIE, M, HULTÉN, M
المصدر: Annals of Human Genetics. 56(3)
مصطلحات موضوعية: Biological Sciences, Genetics, Animals, Base Sequence, Chromosome Mapping, Chromosomes, Human, Pair 9, DNA, Single-Stranded, Genetic Linkage, Humans, Mice, Molecular Sequence Data, Tuberous Sclerosis, chromosomal localization, chromosome 9, chromosome 9p, chromosome 9q, chromosome analysis, chromosome map, conference paper, friedreich ataxia, gene, gene mapping, genetic linkage, genetic polymorphism, human, major clinical study, normal human, priority journal, pulsed field gel electrophoresis, telomere, torsion dystonia, tuberous sclerosis, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/5k97g95tTest
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5دورية أكاديمية
المؤلفون: Povey, S, Smith, M, Haines, J, Kwiatkowski, D, Fountain, J, Bale, A, Abbott, C, Jackson, I, Lawrie, M, Hultén, M
المصدر: Annals of human genetics. 56(3)
مصطلحات موضوعية: Chromosomes, Human, Pair 9, Animals, Humans, Mice, Tuberous Sclerosis, DNA, Single-Stranded, Chromosome Mapping, Base Sequence, Molecular Sequence Data, Genetic Linkage, chromosomal localization, chromosome 9, chromosome 9p, chromosome 9q, chromosome analysis, chromosome map, conference paper, friedreich ataxia, gene, gene mapping, genetic linkage, genetic polymorphism, human, major clinical study, normal human, priority journal, pulsed field gel electrophoresis, telomere, torsion dystonia, tuberous sclerosis, Genetics & Heredity, Clinical Sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/5k97g95tTest
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6دورية أكاديمية
المؤلفون: JANSSEN, LAJ, POVEY, S, ATTWOOD, J, SANDKUYL, LA, LINDHOUT, D, FLODMAN, P, SMITH, M, SAMPSON, JR, HAINES, JL, MERKENS, EC, FLEURY, P, SHORT, P, AMOS, J, HALLEY, DJJ
المصدر: Annals of the New York Academy of Sciences. 615(1)
مصطلحات موضوعية: Biological Sciences, Genetics, Chromosome Mapping, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 9, Genes, Genetic Linkage, Humans, Likelihood Functions, Tuberous Sclerosis, chromosome 11q, chromosome 9q, conference paper, female, genetic heterogeneity, genetic linkage, human, male, priority journal, tuberous sclerosis, Genes, Structural, Human, Linkage, Support, Non-U.S. Gov't, General Science & Technology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/6r63j272Test
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7دورية أكاديمية
المؤلفون: Baumann, R, Smith, M
المصدر: Nucleic acids research. 18(3)
مصطلحات موضوعية: Chromosomes, Human, Pair 9, Humans, Deoxyribonucleases, Type II Site-Specific, Proto-Oncogene Proteins c-abl, Proto-Oncogene Proteins, Chromosome Mapping, Gene Frequency, Polymorphism, Restriction Fragment Length, Chromosomes, Human, Pair 9, Deoxyribonucleases, Type II Site-Specific, Polymorphism, Restriction Fragment Length, chromosomal localization, chromosome 9q, codominance, gene frequency, genetic engineering, heredity, human, human cell, note, oncogene, priority journal, restriction fragment length polymorphism, Developmental Biology, Environmental Sciences, Biological Sciences, Information and Computing Sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/9bv864dvTest
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8
المؤلفون: Junli Zhang, Qiu Rao, Zhihong Zhang, Yuxi Gong, Qiuyuan Xia, Pan Ji, Chunni Chen, Xiang Zhang, B Y Zhai, Yefan Yang, Yang Shao, Xiao Li, Liuqing Zhu
المصدر: Diagnostic Pathology
Diagnostic Pathology, Vol 16, Iss 1, Pp 1-11 (2021)مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, China, Histology, DNA Mutational Analysis, Biology, Lymphoma, T-Cell, Pathology and Forensic Medicine, JAK-STAT pathway, Intestinal Neoplasms, Exome Sequencing, medicine, Biomarkers, Tumor, STAT5 Transcription Factor, RB1-214, Humans, Genetic Predisposition to Disease, Monomorphic epitheliotropic intestinal T-cell lymphoma, Aged, Retrospective Studies, Aged, 80 and over, Chinese population, Intestinal T-cell lymphoma, Research, Gene Amplification, Janus Kinase 3, General Medicine, Middle Aged, Phenotype, Whole-exome sequencing, Mutation, Female, Chromosomes, Human, Pair 9, Amplification of chromosome 9q
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f23f1f9b80398bd5f21e143e5e878c3dTest
http://europepmc.org/articles/PMC8667391Test -
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المؤلفون: Chunni Chen (1616026), Yuxi Gong (11828529), Yefan Yang (11828532), Qiuyuan Xia (5226149), Qiu Rao (584813), Yang Shao (511623), Liuqing Zhu (10029401), Junli Zhang (431927), Xiao Li (107004), Pan Ji (192141), Boya Zhai (8871041), Xiang Zhang (19800), Zhihong Zhang (2027)
مصطلحات موضوعية: Medicine, Cell Biology, Genetics, Cancer, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Monomorphic epitheliotropic intestinal T-cell lymphoma, Whole-exome sequencing, JAK-STAT pathway, Amplification of chromosome 9q
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10
المؤلفون: Chunni Chen (1616026), Yuxi Gong (11828529), Yefan Yang (11828532), Qiuyuan Xia (5226149), Qiu Rao (584813), Yang Shao (511623), Liuqing Zhu (10029401), Junli Zhang (431927), Xiao Li (107004), Pan Ji (192141), Boya Zhai (8871041), Xiang Zhang (19800), Zhihong Zhang (2027)
مصطلحات موضوعية: Medicine, Cell Biology, Genetics, Cancer, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Monomorphic epitheliotropic intestinal T-cell lymphoma, Whole-exome sequencing, JAK-STAT pathway, Amplification of chromosome 9q