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1. Full Text Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors
by Avet-Loiseau, Hervé and Gerson, Fabienne and Magrangeas, Florence and Minvielle, Stéphane and Harousseau, Jean-Luc and Bataille, Régis and Intergrp Francophone Myelome and Intergroupe Francophone du Myélome
Blood, ISSN 0006-4971, 11/2001, Volume 98, Issue 10, pp. 3082 - 3086
Life Sciences & Biomedicine | Hematology | Science & Technology | Immunopathology | Biological and medical sciences | Immunoglobulinopathies | Medical sciences | Immunodeficiencies. Immunoglobulinopathies | Chromosomes, Human, Pair 13 - genetics | Chromosomes, Human, Pair 8 - genetics | Translocation, Genetic | Chromosomes, Human, Pair 13 - ultrastructure | Chromosomes, Artificial, Yeast | Humans | Plasmacytoma - genetics | Paraproteinemias - genetics | Genes, myc | Chromosomes, Human, Pair 4 - genetics | Leukemia, Plasma Cell - genetics | Chromosomes, Human, Pair 4 - ultrastructure | Tumor Cells, Cultured | Neoplasm Proteins - genetics | Chromosomes, Human, Pair 8 - ultrastructure | Disease Models, Animal | Leukemia, Plasma Cell - blood | Multiple Myeloma - blood | Chromosome Deletion | DNA Probes | Chromosomes, Human, Pair 11 - ultrastructure | Interphase | beta 2-Microglobulin - analysis | In Situ Hybridization, Fluorescence | Chromosomes, Human, Pair 11 - genetics | Genes, Immunoglobulin | Multiple Myeloma - pathology | Animals | Gene Rearrangement, B-Lymphocyte, Heavy Chain | Neoplasm Proteins - blood | Chromosomes, Human, Pair 14 - ultrastructure | Mice | Paraproteinemias - blood | Chromosomes, Human, Pair 14 - genetics | Immunoglobulin Heavy Chains - genetics | Multiple Myeloma - genetics | Cohort Studies | Index Medicus | Abridged Index Medicus
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2. Full Text Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk
by Ji, X and Bossé, Y and Landi, M.T and Gui, Jiang and Xiao, X and Qian, D.C and Kiemeney, L.A.L.M and Heijden, E. van der and Brennan, P and Amos, C.I and et al
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 3221 - 15
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Lung Neoplasms - genetics | Smoking - adverse effects | Genetic Predisposition to Disease | Reproducibility of Results | Humans | Middle Aged | Risk Factors | Child, Preschool | Infant | Male | Chromosomes, Human, Pair 15 - genetics | Gene Regulatory Networks | Young Adult | Adolescent | Adult | Female | Aged | Polymorphism, Single Nucleotide | Child | Gene Ontology | Infant, Newborn | Cohort Studies | Quantitative Trait Loci - genetics | Channel gating | Lung cancer | Health risks | Risk | Genomes | Single-nucleotide polymorphism | Loci | Quantitative trait loci | Annotations | Pathways | Etiology | Ligands | Health risk assessment | Chromosome 15 | Chromosomes | Cancer | Index Medicus | Clinical Medicine | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Cancer and Oncology | Cancer och onkologi
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3. Full Text Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
by Lan, Qing and Hsiung, Chao A and Matsuo, Keitaro and Hong, Yun-Chul and Seow, Adeline and Wang, Zhaoming and Hosgood, H. Dean and Chen, Kexin and Wang, Jiu-Cun and Chatterjee, Nilanjan and Hu, Wei and Wong, Maria Pik and Zheng, Wei and Caporaso, Neil and Park, Jae Yong and Chen, Chien-Jen and Kim, Yeul Hong and Kim, Young Tae and Landi, Maria Teresa and Shen, Hongbing and Lawrence, Charles and Burdett, Laurie and Yeager, Meredith and Yuenger, Jeffrey and Jacobs, Kevin B and Chang, I-Shou and Mitsudomi, Tetsuya and Kim, Hee Nam and Chang, Gee-Chen and Bassig, Bryan A and Tucker, Margaret and Wei, Fusheng and Yin, Zhihua and Wu, Chen and An, She-Juan and Qian, Biyun and Lee, Victor Ho Fun and Lu, Daru and Liu, Jianjun and Jeon, Hyo-Sung and Hsiao, Chin-Fu and Sung, Jae Sook and Kim, Jin Hee and Gao, Yu-Tang and Tsai, Ying-Huang and Jung, Yoo Jin and Guo, Huan and Hu, Zhibin and Hutchinson, Amy and Wang, Wen-Chang and Klein, Robert and Chung, Charles C and Oh, In-Jae and Chen, Kuan-Yu and Berndt, Sonja I and He, Xingzhou and Wu, Wei and Chang, Jiang and Zhang, Xu-Chao and Huang, Ming-Shyan and Zheng, Hong and Wang, Junwen and Zhao, Xueying and Li, Yuqing and Choi, Jin Eun and Su, Wu-Chou and Park, Kyong Hwa and Sung, Sook Whan and Shu, Xiao-Ou and Chen, Yuh-Min and Liu, Li and Kang, Chang Hyun and Hu, Lingmin and Chen, Chung-Hsing and Pao, William and Kim, Young-Chul and Yang, Tsung-Ying and Xu, Jun and Guan, Peng and Tan, Wen and Su, Jian and Wang, Chih-Liang and Li, Haixin and Sihoe, Alan Dart Loon and Zhao, Zhenhong and Chen, Ying and Choi, Yi Young and Hung, Jen-Yu and Kim, Jun Suk and Yoon, Ho-Il and Cai, Qiuyin and Lin, Chien-Chung and Park, In Kyu and Xu, Ping and Dong, Jing and Kim, Christopher and He, Qincheng and Perng, Reury-Perng and Kohno, Takashi and Kweon, Sun-Seog and ...
Nature genetics, ISSN 1061-4036, 12/2012, Volume 44, Issue 12, pp. 1330 - 1335
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Tumors of the respiratory system and mediastinum | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Pneumology | Lung Neoplasms - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Adenocarcinoma of Lung | Carcinoma, Squamous Cell - genetics | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Genetic Loci | Chromosomes, Human, Pair 15 - genetics | Chromosomes, Human, Pair 6 - genetics | Chromosomes, Human, Pair 17 | Adult | Female | Adenocarcinoma - genetics | Aged | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 10 - genetics | Chromosomes, Human, Pair 5 - genetics | Smoking | Women | Lung cancer | Physiological aspects | Disease susceptibility | Genetic aspects | Research | Single nucleotide polymorphisms | Chromosomes | Health aspects | Studies | Confidence intervals | Tobacco smoke | Genomes | Epidemiology | Index Medicus
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4. Full Text Novel microdeletion syndromes detected by chromosome microarrays
by Slavotinek, Anne M
Human genetics, ISSN 0340-6717, 8/2008, Volume 124, Issue 1, pp. 1 - 17
Gene Function | Human Genetics | Molecular Medicine | Biomedicine | Metabolic Diseases | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Human | Complex syndromes | Medical genetics | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Chromosome Deletion | Gene Duplication | Oligonucleotide Array Sequence Analysis | Humans | Chromosomes, Human, Pair 9 | Syndrome | Chromosomes, Human, Pair 2 | Chromosomes, Human, Pair 1 | Chromosomes, Human, Pair 17 | Abnormalities, Multiple - diagnosis | Chromosome Mapping - methods | Chromosomes, Human, Pair 15 | Chromosomes, Human, Pair 16 | Abnormalities, Multiple - genetics | Index Medicus
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5. Full Text A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
by Ng, Daniel P K and Lauritzen, Torsten and Fujita, Hayato and Kubo, Michiaki and Park, Kyong Soo and Ma, Ronald C W and Okada-Iwabu, Miki and Watada, Hirotaka and Sandbæk, Annelli and Maeda, Shiro and Kadowaki, Takashi and Hara, Kazuo and Grarup, Niels and Shojima, Nobuhiro and Andersen, Gitte and Yamauchi, Toshimasa and Tsunoda, Tatsuhiko and Horikoshi, Momoko and Nakamura, Yusuke and So, Wing-Yee and Beury, Delphine and Tai, E Shyong and Ohshige, Toshihiko and Kashiwagi, Atsunori and Shin, Hyoung Doo and Ito, Chikako and Cauchi, Stephane and Hansen, Torben and Chan, Juliana C N and Iwabu, Masato and Hirose, Hiroshi and Takahashi, Atsushi and Froguel, Philippe and Omori, Shintaro and Tanaka, Yasushi and Kaku, Kohei and Kamatani, Naoyuki and Maegawa, Hiroshi and Saito, Ikuo and Witte, Daniel R and Nakamura, Masahiro and Pedersen, Oluf and Kasuga, Masato and Yasuda, Kazuki and Jørgensen, Torben and Kawamori, Ryuzo
Nature genetics, ISSN 1061-4036, 10/2010, Volume 42, Issue 10, pp. 864 - 868
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Diabetes. Impaired glucose tolerance | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Genetic Predisposition to Disease | Genome-Wide Association Study | Diabetes Mellitus, Type 2 - genetics | Humans | Asian Continental Ancestry Group - genetics | Genotype | Ubiquitin-Conjugating Enzymes - genetics | Transcription Factors - genetics | Chromosomes, Human, Pair 15 - genetics | Case-Control Studies | Polymorphism, Single Nucleotide - genetics | Genome, Human | Chromosomes, Human, Pair 3 - genetics | Quantitative trait loci | Type 2 diabetes | Genetic susceptibility | Demographic aspects | Genetic aspects | Research | Risk factors | Studies | Research & development--R&D | Genomics | Technological change | Genetics | Grants | Diabetes | Index Medicus
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6. Full Text Embryo morphology and development are dependent on the chromosomal complement
by Magli, M. Cristina, M.Sc and Gianaroli, Luca, M.D and Ferraretti, Anna Pia, M.D., Ph.D and Lappi, Michela, B.Sc and Ruberti, Alessandra, B.Sc and Farfalli, Valeria, M.D
Fertility and sterility, ISSN 0015-0282, 2007, Volume 87, Issue 3, pp. 534 - 541
Internal Medicine | Obstetrics and Gynecology | fluorescence in situ hybridization | chromosomal abnormalities | Aneuploidy | embryo morphology | preimplantation genetic diagnosis | cleavage rate | blastomere biopsy | embryo fragmentation | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Gynecology. Andrology. Obstetrics | Biological and medical sciences | Medical sciences | Chromosome aberrations | Medical genetics | Chromosomes, Human, Pair 13 - genetics | Chromosomes, Human, X - genetics | Humans | Embryonic Development - genetics | Preimplantation Diagnosis | In Situ Hybridization, Fluorescence | Chromosomes, Human, Pair 15 - genetics | Chromosomes, Human, Pair 21 - genetics | Chromosomes, Human, Y - genetics | Pregnancy | Chromosomes, Human, Pair 22 - genetics | Fertilization in Vitro | Embryo, Mammalian - anatomy & histology | Sex Chromosome Aberrations | Biopsy | Chromosome Aberrations | Adult | Female | Retrospective Studies | Chromosomes, Human, Pair 18 - genetics | Chromosomes, Human, Pair 16 - genetics | Embryo | Index Medicus
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7. Full Text Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
by Depienne, Christel and Moreno-De-Luca, Daniel and Heron, Delphine and Bouteiller, Delphine and Gennetier, Aurélie and Delorme, Richard and Chaste, Pauline and Siffroi, Jean-Pierre and Chantot-Bastaraud, Sandra and Benyahia, Baya and Trouillard, Oriane and Nygren, Gudrun and Kopp, Svenny and Johansson, Maria and Rastam, Maria and Burglen, Lydie and Leguern, Eric and Verloes, Alain and Leboyer, Marion and Brice, Alexis and Gillberg, Christopher and Betancur, Catalina and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Biological psychiatry (1969), ISSN 0006-3223, 2009, Volume 66, Issue 4, pp. 349 - 359
Psychiatry | Autism | Angelman syndrome | MLPA | deletion | chromosome 15 | duplication | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Complex syndromes | Malformations of the nervous system | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Medical genetics | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Autistic Disorder - genetics | Humans | Child, Preschool | Uniparental Disomy | Male | DNA Methylation - genetics | Gene Dosage | Chromosomes, Human, Pair 15 - genetics | Microsatellite Repeats - genetics | Gene Deletion | Adolescent | Chromosome Aberrations | Angelman Syndrome - genetics | Prader-Willi Syndrome - genetics | Adult | Female | Child | Prader-Willi syndrome | Methylation | Cardiac patients | Index Medicus | Autistic Disorder | Life Sciences | DNA Methylation | Chromosomes, Human, Pair 15 | Genetics | Angelman Syndrome | Microsatellite Repeats | Prader-Willi Syndrome | Human | Preschool | Psykiatri | Chromosomes | Pair 15
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