المؤلفون: Hatadani, Luciane Mendes

المساهمون: Klaczko, Louis Bernard, 1953, Azeredo-Espin, Ana Maria Lima de, 1955, Reis, Sérgio Furtado dos, Carvalho, Antonio Bernardo de, Manfrin, Sergio Russo, Linhares, Arício Xavier, Universidade Estadual de Campinas. Instituto de Biologia, Programa de Pós-Graduação em Genética e Biologia Molecular, UNIVERSIDADE ESTADUAL DE CAMPINAS

المصدر: Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP

مصطلحات موضوعية: Temperatura corporal, Filogenia, Inversion, chromosome, Wings (Anatomy), Asas (Anatomia), Drosophila, Body temperature, Inversão cromossômica, Phylogeny

وصف الملف: application/pdf; 121p. : il.

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::737745d7c237398267ffe3a90e4d7496
https://doi.org/10.47749/t/unicamp.2007.417284

المؤلفون: KAYA, Murat

المصدر: Volume: 3, Issue: 3 112-114
Ahi Evran Medical Journal

مصطلحات موضوعية: Tekrarlayan düşükler,perisentrik inversiyon,kromozom anomalisi, Medicine, Miscarriages,pericentric inversion,chromosome abnormality, Tıp

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=tubitakulakb::d7d064a97c9e856c50473ad11b66413e
https://dergipark.org.tr/tr/pub/aemj/issue/50453/544440

المؤلفون: KAYA, Murat

المصدر: Volume: 3, Issue: 3 112-114 ; 2619-9203 ; Ahi Evran Medical Journal

مصطلحات موضوعية: Miscarriages,pericentric inversion,chromosome abnormality, Tekrarlayan düşükler,perisentrik inversiyon,kromozom anomalisi

وصف الملف: application/pdf

Relation: https://dergipark.org.tr/tr/download/article-file/873659; https://dergipark.org.tr/tr/pub/aemj/issue/50453/544440

الاتاحة: https://dergipark.org.tr/tr/pub/aemj/issue/50453/544440

المؤلفون: Esteban Hasson, Juan Jose Fanara, Paula Lipko, Ignacio Maria Soto

المصدر: Neotropical Entomology. 45:333-335

مصطلحات موضوعية: Inversion Chromosome Polymorphism, 0106 biological sciences, 0301 basic medicine, Entomology, Range (biology), Otras Ciencias Biológicas, Argentina, 010603 evolutionary biology, 01 natural sciences, Ciencias Biológicas, 03 medical and health sciences, Drosophilidae, Botany, Animals, Cactophilic flies, Drosophila, Genetic diversity, biology, Castus Host, Host (biology), Genetic Variation, biology.organism_classification, Melon, 030104 developmental biology, Evolutionary biology, Insect Science, Cactus, Cucumis, CIENCIAS NATURALES Y EXACTAS

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac6012352ee68ef8f4b85dbcafe6a6f4
https://doi.org/10.1007/s13744-016-0373-2

المؤلفون: TANRIVERDİ, Nilgün, PAZARBAŞI, Ayfer, KARAHAN, Dilara, AVCI, Ayşe, TAHİROĞLU, Ayşegül Yolga, TUNÇ, Erdal, DEMİRHAN, Osman

المصدر: Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 38, Iss 1, Pp 108-113 (2013)
Volume: 38, Issue: 1 108-113
Cukurova Medical Journal

مصطلحات موضوعية: Pericentric inversion, lcsh:R5-920, lcsh:R, Pericentric inversion,Chromosome 10p-q,Aggressive behavior,Hyperactivity,Mental retardation, Aggressive behavior, lcsh:Medicine, Mental retardation, Perisentrik inversiyon,Kromozom 10p-q,Agresif davranış,Hiperaktiflik,Mental retardasyon, lcsh:Medicine (General), Chromosome 10p-q, Hyperactivity

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::27ba088681c18f8d677edd1429ad008f
http://www.scopemed.org/fulltextpdf.php?mno=26243

المؤلفون: John C K Barber, Kathryn Watts, Thomas Liehr, Reiner Siebert, N. Simon Thomas, Zeynep Tümer, Simone Heidemann, Jens Michael Hertz, Victoria Bryant, Ina Fickelscher

المصدر: Fickelscher, I, Liehr, T, Watts, K, Bryant, V, Barber, J C K, Heidemann, S, Siebert, R, Hertz, J M, Tumer, Z & Simon Thomas, N 2007, ' The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity. ', American Journal of Human Genetics, vol. 81, no. 4, pp. 847-56 . https://doi.org/10.1086/521226

مصطلحات موضوعية: Chromosomes, Artificial, Bacterial, Inversion, Chromosome, Sequence analysis, Variation (Genetics), Biology, 03 medical and health sciences, Report, Genetics, medicine, Humans, Genetics(clinical), In Situ Hybridization, Fluorescence, Genetics (clinical), 030304 developmental biology, Segmental duplication, Chromosomal inversion, Gene Rearrangement, 0303 health sciences, medicine.diagnostic_test, 030305 genetics & heredity, Haplotype, Breakpoint, Genetic Variation, Chromosome Breakage, Gene rearrangement, Haplotypes, Chromosomes, Human, Pair 2, Karyotyping, Chromosome Inversion, Chromosome breakage, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ad6e428427cadfd1330b5140c53d416
https://doi.org/10.1086/521226

المؤلفون: C. Charrin, Anne Hagemeijer, Carole Barin, M J Mozzicconacci, Barbara Cauwelier, Christine Lefebvre, Bruno Verhasselt, Isabelle Luquet, M.J. Gregoire, Philippe Jonveaux, Hélène Cavé, Barbara De Moerloose, Christine Terré, Kim De Keersmaecker, Anne De Paepe, G Plessis, F Sigaux, Nicole Dastugue, Bruce Poppe, Michel Lessard, B Laurence, Laurent Mauvieux, Hélène Antoine-Poirel, Marina Lafage-Pochitaloff, Francine Mugneret, Emmanuelle Clappier, J van den Akker, J Soulier, C Graux, Yves Benoit, Jan Cools, Carine Gervais, Franki Speleman, Pascale Cornillet-Lefebvre, Marie-Pierre Pages, C Chalas, Dominique Leroux, N. Van Roy, Christine Perot, Pierre Heimann, Roland Berger

المساهمون: Center for Medical Genetics [Ghent], Ghent University Hospital, Laboratoire de Biochimie Génétique, Hôpital Robert Debré, Laboratoire d'Hématologie, CHU Strasbourg, CHU Bretonneau, Centre de Recherche Saint-Antoine (UMRS893), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU Dijon, Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Laboratoire Central d'Anatomie et de Cytologie Pathologiques [Hôpital Edouard Herriot - HCL], Hôpital Edouard Herriot [CHU - HCL], Hospices Civils de Lyon (HCL)-Hospices Civils de Lyon (HCL), Service de Génétique [CHRU Nancy], Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC), Centre Hospitalier de Versailles André Mignot (CHV), Hôpital Maison Blanche, Centre Hospitalier Universitaire de Reims (CHU Reims), Hôpital Robert Debré-Centre Hospitalier Universitaire de Reims (CHU Reims), Service de Génétique [CHU Caen], Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), Bases moléculaires de la progression tumorale -Groupe de Recherche sur les Lymphomes, Université Joseph Fourier - Grenoble 1 (UJF)-Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR73, Centre for Medical genetics, Hôpital UCL-St Luc, Gvh et Gvl : Physiopathologie Chez l'Homme et Chez l'Animal, Incidence et Role Therapeutique, Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Medical Genetics, Hôpital Erasme [Bruxelles] (ULB), Faculté de Médecine [Bruxelles] (ULB), Université libre de Bruxelles (ULB)-Université libre de Bruxelles (ULB)-Faculté de Médecine [Bruxelles] (ULB), Université libre de Bruxelles (ULB)-Université libre de Bruxelles (ULB), Centre for Molecular Diagnostics, Department of Pediatric Hematology/Oncology, Department of Human Genetics, Flanders Interuniversity Institute for Biotechnology (VIB), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Centre for Human Genetics, Hôpital Purpan [Toulouse], CHU Toulouse [Toulouse]-CHU Toulouse [Toulouse], Service Hématologie - IUCT-Oncopole [CHU Toulouse], Pôle Biologie [CHU Toulouse], Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Pôle IUCT [CHU Toulouse], Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Centre for Medical Genetics, Centre de Recherche Saint-Antoine (CR Saint-Antoine), Université Pierre et Marie Curie - Paris 6 (UPMC) - Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Universitaire de Dijon (CHU Dijon), Laboratoire de Cytopathologie, Hôpital Edouard Herriot, Laboratoire de Génétique, CHU Nancy, Institut Paoli Calmettes, CHU Versailles, Centre Hospitalier de Versailles (CHV), CHU Reims, Hôpital Robert Debré - CHU Reims, Service de génétique, CHU Caen - Hôpital Clémenceau, Université Joseph Fourier - Grenoble 1 (UJF) - Institut National de la Santé et de la Recherche Médicale (INSERM) - IFR73, Université Paris Diderot - Paris 7 (UP7) - Institut National de la Santé et de la Recherche Médicale (INSERM), University Hospital Erasme, Hôpital Necker - Enfants malades, Assistance publique - Hôpitaux de Paris (AP-HP) - Université Paris Descartes - Paris 5 (UPD5), Hôpital Purpan, Duley, Samuel

المصدر: Leukemia
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. <10.1038/sj.leu.2404410>

مصطلحات موضوعية: Male, Cancer Research, Receptors, Antigen, T-Cell, alpha-beta, [SDV.GEN] Life Sciences [q-bio]/Genetics, MESH: Receptor, Notch1, Translocation, Genetic, 0302 clinical medicine, Immunophenotyping, MESH: Child, Leukemia-Lymphoma, Adult T-Cell, MESH: Leukemia-Lymphoma, Adult T-Cell, Receptor, Notch1, Child, Chromosomal inversion, 0303 health sciences, MESH: Middle Aged, MESH: Receptors, Antigen, T-Cell, alpha-beta, hemic and immune systems, Hematology, Middle Aged, MESH: Gene Rearrangement, T-Lymphocyte, MESH: Translocation, Genetic, 3. Good health, Oncology, 030220 oncology & carcinogenesis, Female, Chromosome Deletion, Adult, Transcriptional Activation, medicine.medical_specialty, Adolescent, MESH: Immunophenotyping, MESH: Chromosome Deletion, chemical and pharmacologic phenomena, Chromosomal rearrangement, Biology, Gene Rearrangement, T-Lymphocyte, 03 medical and health sciences, Acute lymphocytic leukemia, MESH: Homeodomain Proteins, medicine, Humans, 030304 developmental biology, Homeodomain Proteins, MESH: Adolescent, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, T-cell receptor, Cytogenetics, MESH: Adult, Gene rearrangement, medicine.disease, Molecular biology, MESH: Male, Homeobox A10 Proteins, Chromosome Inversion, MESH: Inversion, Chromosome, MESH: Transcriptional Activation, MESH: Female, Comparative genomic hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be0e2a8fa5b81d3b8f190bc9464a5df5
https://doi.org/10.1038/sj.leu.2404410

المؤلفون: Zhengdong D. Zhang, Jun Wang, Zhu Chen, Will Gillett, George M. Weinstock, Guoping Zhao, LaRonda Jackson, Christopher K. Raymond, Manuel L. Gonzalez-Garay, Yang Zhou, Judith Hernandez, Boqin Qiang, James B. Clendenning, Zhijian J. Chen, Shannon Dugan-Rocha, Andrew R. Jackson, Zhijian Yao, Yan Shen, R. Alan Harris, Ziad Khan, Margaret Morgan, Wei Dong, Sharon Wei, Dawn Garcia, Aleksandar Milosavljevic, Maynard V. Olson, Ruben Rodriguez, Kerstin P. Clerc-Blankenburg, Ryan J. Lozado, Ralf Sudbrak, Jun Gu, Jing Kun Zhang, Heather R. Draper, Mary J. Brown, Channakhone Saenphimmachak, M. Ali Ansari-Lari, Songnian Hu, Preethi H. Gunaratne, Donna M. Muzny, Shiran Pasternak, Xing Zhi Song, Oliver Delgado, Bailin Hao, Lesette Perez, Charles Q. Adams, Michael L. Metzker, Anne Hodgson, Daniel Verduzco, Bao Viet Nguyen, Susan H. Kelly, Xin He, Jing Wang, Runsheng Chen, Karen A. Phelps, Rajinder Kaul, Guan Chen, Wei Huang, Huyen Dinh, Lenee Waldron, Paul Havlak, George Miner, Qiaoyan Wang, Ye Yuan, Rachel Gill, Anthony Palmeiri, Mathew W. Wright, Kim C. Worley, Michael Kube, Jing Liu, Clay Davis, Christian J. Buhay, Zhangwan Li, Jun Yu, Alicia Hawes, Jing Lu, Steffen Hennig, David L. Nelson, Rui Chen, Leni S. Jacob, Huanming Yang, Bin Liu, Steven E. Scherer, Christie Kovar-Smith, Jian Wang, Manjula Maheshwari, Gabrielle A. Williams, Paul E. Tabor, David A. Wheeler, Hans Lehrach, Graham R. Scott, Farah J.H. Plopper, Erica Sodergren, Wen Liu, Mulu Ayele, Richard Reinhardt, Richard A. Gibbs, Eric Haugen, Lora Lewis, Hua Shen, Gang Fu, Jianling Zhou, Xiuqing Zhang, Stephen Ernst, Geoffrey Okwuonu, Susan L. Naylor, Jennifer Hume, Ruth Levy, Andrew Cree, Yan Ding, David Steffen, Lynne V. Nazareth, Jireh Santibanez, Sandhya Subramanian, Gane Ka-Shu Wong

المصدر: Muzny, D M, Scherer, S E, Kaul, R, Wang, J, Yu, J, Sudbrak, R, Buhay, C J, Chen, R, Cree, A, Ding, Y, Dugan-Rocha, S, Gill, R, Gunaratne, P, Harris, R A, Hawes, A C, Hernandez, J, Hodgson, A V, Hume, J, Jackson, A, Khan, Z M, Kovar-Smith, C, Lewis, L R, Lozado, R J, Metzker, M L, Milosavljevic, A, Miner, G R, Morgan, M B, Nazareth, L V, Scott, G, Sodergren, E, Song, X-Z, Steffen, D, Wei, S, Wheeler, D A, Wright, M W, Worley, K C, Yuan, Y, Zhang, Z, Adams, C Q, Ansari-Lari, M A, Ayele, M, Brown, M J, Chen, G, Chen, Z, Clendenning, J, Clerc-Blankenburg, K P, Chen, R, Chen, Z, Davis, C, Delgado, O, Dinh, H H, Dong, W, Draper, H, Ernst, S, Fu, G, Gonzalez-Garay, M L, Garcia, D K, Gillett, W, Gu, J, Hao, B, Haugen, E, Havlak, P, He, X, Hennig, S, Hu, S, Huang, W, Jackson, L R, Jacob, L S, Kelly, S H, Kube, M, Levy, R, Li, Z, Liu, B, Liu, J, Liu, W, Lu, J, Maheshwari, M, Nguyen, B-V, Okwuonu, G O, Palmeiri, A, Pasternak, S, Perez, L M, Phelps, K A, Plopper, F J H, Qiang, B, Raymond, C, Rodriguez, R, Saenphimmachak, C, Santibanez, J, Shen, H, Shen, Y, Subramanian, S, Tabor, P E, Verduzco, D, Waldron, L, Wang, J, Wang, J, Wang, Q, Williams, G A, Wong, G K-S, Yao, Z, Zhang, J, Zhang, X, Zhao, G, Zhou, J, Zhou, Y, Nelson, D, Lehrach, H, Reinhardt, R, Naylor, S L, Yang, H, Olson, M, Weinstock, G & Gibbs, R A 2006, ' The DNA sequence, annotation and analysis of human chromosome 3 ', Nature, vol. 440, no. 7088, pp. 1194-1198 . https://doi.org/10.1038/nature04728

مصطلحات موضوعية: Inversion, Chromosome, Genome evolution, DNA, Complementary, Pan troglodytes, Molecular Sequence Data, Biology, Synteny, Genome, Evolution, Molecular, Chimpanzee genome project, Contig Mapping, Chromosome 19, Human Genome Project, Animals, Humans, Expressed Sequence Tags, Genetics, Multidisciplinary, Base Sequence, Chromosome Breakage, Sequence Analysis, DNA, Genome project, Macaca mulatta, Chromosome Inversion, CpG Islands, Human genome, Chromosomes, Human, Pair 3, Chromosome 21, Reference genome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd780c357efa6aedc628e163a245045d
https://doi.org/10.1038/nature04728

المؤلفون: Joann Bodurtha, Teresa Costa, Martin Li, Barbara R. Pober, Stephen W. Scherer, Ariane Mandel, Sarah R. Cox, Lucy R. Osborne, Lap-Chee Tsui, Theresa A. Grebe, David Chitayat

المصدر: Nature Genetics. 29:321-325

مصطلحات موضوعية: Genetic Markers, Male, Williams Syndrome, Proband, congenital, hereditary, and neonatal diseases and abnormalities, Electrophoresis, gel, pulsed-field, Adolescent, Genotype, Molecular Sequence Data, Population, Biology, Article, Polymorphism, genetic - genetics, Genetics, medicine, Humans, Genetic Predisposition to Disease, cardiovascular diseases, education, In Situ Hybridization, Fluorescence, Chromosomal inversion, education.field_of_study, Polymorphism, Genetic, medicine.diagnostic_test, Physical Chromosome Mapping, Infant, Chromosome, medicine.disease, Phenotype, Inversion, chromosome, Chromosome Inversion, Mutation, Williams syndrome - genetics, Female, Williams syndrome, Chromosomes, human, pair 7 - genetics, Haploinsufficiency, Chromosomes, Human, Pair 7, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54518c2ed2f0fea565b39c6c574a21ed
https://doi.org/10.1038/ng753

المؤلفون: Shannon McDermott

مصطلحات موضوعية: x-linked genes,x-linked disorders,x inactivation,trisomy,translocation,sex-linked genes,sex-linked disorder,sex chromosomes,sex chromosome,polyploidy,polyploid,pericentric,paracentric,nondisjunction,monosomy,karyotype,karyogram,inherited disorder,inheritance,genetics,euploid,chromosome number disorder,chromosome nondisjunction,chromosome inversion,chromosome identification,chromosome disorder,chromosome aberration,chromosome 18 inversion,autosome,autosomal chromosome,aneuploidy,aneuploid

Relation: http://cnx.org/contents/7baa9f17-bddc-4107-a061-6481e296a047@2

الاتاحة: http://cnx.org/contents/7baa9f17-bddc-4107-a061-6481e296a047@2

المؤلفون: Marina Narbaitz, Maria Fernanda Noriega, Roxana Cerretini, María Fernanda Palacios, Irma Slavutsky, Pedro Negri, Estela Marta Pedrazzini, Raquel Bengió

المصدر: Cancer genetics and cytogenetics. 167(2)

مصطلحات موضوعية: Adult, Male, Cancer Research, CIENCIAS MÉDICAS Y DE LA SALUD, Derivative chromosome, Medicina Clínica, Lymphoma, Mantle-Cell, Biology, Polymerase Chain Reaction, law.invention, FISH, law, Genetics, medicine, Humans, Molecular Biology, Polymerase chain reaction, In Situ Hybridization, Fluorescence, Chromosomal inversion, Aged, MANTLE CELL LYMPHOMA, Aged, 80 and over, medicine.diagnostic_test, Breakpoint, KARYOTYPE, INVERSION CHROMOSOME 2, Karyotype, INVERSION CHROMOSOME 6, medicine.disease, Molecular biology, Lymphoma, Chromosomes, Human, Pair 2, Karyotyping, Chromosome Inversion, Mantle cell lymphoma, Chromosomes, Human, Pair 6, Female, Medicina Critica y de Emergencia, Fluorescence in situ hybridization

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcfdb319382ec5417bb58087dc4265e2
https://pubmed.ncbi.nlm.nih.gov/16737918

المؤلفون: Mirella Marangoni, Arthur Van Aerschot, Jef Rozenski, Piet Herdewijn, Patrick Augustyns

المصدر: Nucleic Acids Research. 25:3034-3041

مصطلحات موضوعية: Inversion, Chromosome, Phosphoramidite, Oligonucleotide, Oligonucleotides, Temperature, Nucleic Acid Hybridization, RNA, Inverse, Biology, Combinatorial chemistry, Thymine, chemistry.chemical_compound, Nucleic acid thermodynamics, Monomer, Biochemistry, chemistry, Chromosome Inversion, Genetics, Nucleic Acid Conformation, DNA, Research Article

وصف الملف: Print

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f632e67d996fdff26a7e3ff6afa2c1
https://doi.org/10.1093/nar/25.15.3034

المؤلفون: CELEP, Figen, KARAGÜZEL, Ahmet

المصدر: Volume: 13, Issue: 1-2 35-37
EASTERN JOURNAL OF MEDICINE

مصطلحات موضوعية: Pericentric inversion chromosome 2

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=tubitakulakb::f6801631f23a9823231b21f441405e4e
https://dergipark.org.tr/tr/pub/ejm/issue/5339/72374

المؤلفون: Mentzer, S E, Sundberg, J P, Awgulewitsch, A, Chao, H H, Carpenter, D A, Zhang, W D, Rinchik, E M, You, Y

المصدر: Faculty Research 2000 - 2009

مصطلحات موضوعية: Chromosome-Mapping, Cloning-Molecular, Ear, Female, Gene-Expression-Regulation, Genotype, Hair, Homeodomain-Proteins, Inversion-Chromosome, Male, Mice, Mutation

Relation: https://mouseion.jax.org/stfb2000_2009/1864; http://www3.interscience.wiley.com/journal/121527164/abstract

الاتاحة: https://mouseion.jax.org/stfb2000_2009/1864
http://www3.interscience.wiley.com/journal/121527164/abstract

المؤلفون: Fantauzzo, K A, Tadin, Strapps M, You, Y, Mentzer, S E, Baumeister, F A, Cianfarani, S, Van, Maldergem L, Warburton, D, Sundberg, J P, Christiano, A M

المصدر: Faculty Research 2000 - 2009

مصطلحات موضوعية: Animals, Binding-Sites, Chromosome-Breakage, Chromosomes-Human-Pair-8, DNA-Binding-Proteins, Disease-Models-Animal, Fluorescent-Antibody-Technique, GATA-Transcription-Factors, Gene-Rearrangement, Hair-Follicle, Humans, Hypertrichosis, In-Situ-Hybridization-Fluorescence, Inversion-Chromosome, Mice, Molecular-Sequence-Data, Phenotype, Polymerase-Chain-Reaction, Sp1-Transcription-Factor, Transcription-Factors, Zinc-Fingers

Relation: https://mouseion.jax.org/stfb2000_2009/1822; http://hmg.oxfordjournals.org/cgi/content/abstract/17/22/3539

الاتاحة: https://mouseion.jax.org/stfb2000_2009/1822
http://hmg.oxfordjournals.org/cgi/content/abstract/17/22/3539

المؤلفون: Ghasemi, Nasrin, Kalantar, Seyed Mehdi, Aflatoonian, Abbas, Tayebi, Naeimeh

مصطلحات موضوعية: Inversion chromosome 9, Recurrent spontaneous abortion, Idiopathic infertility

Relation: http://www.bioline.org.br/abstract?id=mf07011; http://hdl.handle.net/1807/39535

الاتاحة: http://hdl.handle.net/1807/39535
http://www.bioline.org.br/abstract?id=mf07011
http://www.mefsjournal.org; http://www.bioline.org.br/mf

المؤلفون: Pedrazzini, Estela Marta, Cerretini, Roxana, Noriega, Maria Fernanda, Narbaitz, Marina, Palacios, María Fernanda, Negri, Pedro, Bengió, Raquel, Slavutsky, Irma Rosa

مصطلحات موضوعية: Mantle Cell Lymphoma, Karyotype, Fish, Inversion Chromosome 2, Inversion Chromosome 6, https://purl.org/becyt/ford/3.2, https://purl.org/becyt/ford/3

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0165460805007375; http://hdl.handle.net/11336/55898; Pedrazzini, Estela Marta; Cerretini, Roxana; Noriega, Maria Fernanda; Narbaitz, Marina; Palacios, María Fernanda; et al.; Inversions of chromosomes 2 and 6 in mantle cell lymphoma. Cytogenetic, FISH, and molecular studies; Elsevier Science Inc; Cancer Genetics And Cytogenetics; 167; 2; 6-2006; 164-167; CONICET Digital; CONICET

الاتاحة: http://hdl.handle.net/11336/55898

المؤلفون: Hatadani, Luciane Mendes

Thesis Advisors: UNIVERSIDADE ESTADUAL DE CAMPINAS, Azeredo-Espin, Ana Maria Lima de, 1955, Klaczko, Louis Bernard, 1953, Reis, Sérgio Furtado dos, Carvalho, Antonio Bernardo de, Manfrin, Sergio Russo, Linhares, Arício Xavier

المصدر: Repositório Institucional da UnicampUniversidade Estadual de CampinasUNICAMP.

مصطلحات موضوعية: Drosophila, Filogenia, Asas (Anatomia), Inversão cromossômica, Temperatura corporal, Phylogeny, Wings (Anatomy), Inversion, chromosome, Body temperature

وصف الملف: 121p. : il.; application/pdf

الاتاحة: http://repositorio.unicamp.br/jspui/handle/REPOSIP/316981

المؤلفون: Chang, B.S., Düzcan, Füsun., Kim, S., Cinbis, M., Aggarwal, A., Apse, K.A., Ozdel, Osman İsmail., Atmaca, M., Zencir, S., Bagci, H., Walsh, C.A.

مصطلحات موضوعية: Male, Heterozygote, Inversion, Chromosome, Cerebellar hypoplasia, gene locus, Cell Adhesion Molecules, Neuronal, brain development, paracentric chromosome inversion, Nerve Tissue Proteins, preschool child, mental disease, Cytogenetics, Central Nervous System Diseases, Cerebellum, chromosome 7, Humans, human, gene, Child, In Situ Hybridization, Fluorescence, Cerebral Cortex, agyria, clinical article, Extracellular Matrix Proteins, Mental Disorders, Homozygote, Serine Endopeptidases, article, pedigree, Brain, Pachygyria, Magnetic Resonance Imaging, Malformation of cortical development, female, Phenotype, nervous system, priority journal, cerebellum hypoplasia, point mutation, reln gene, Chromosomes, Human, Pair 7

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3566::a7ff17be8daef658846c872e2b11e403
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/4351

المؤلفون: Münevver Atmaca, Bernard S. Chang, Osman Özdel, Füsun Düzcan, Seonhee Kim, Mine Cinbiş, Abha Aggarwal, Kira Apse, Sevil Zencir, Huseyin Bagci, Christopher A. Walsh

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)

مصطلحات موضوعية: Male, Cerebellum, brain development, paracentric chromosome inversion, preschool child, mental disease, Central Nervous System Diseases, Reelin, Child, Genetics (clinical), In Situ Hybridization, Fluorescence, Chromosomal inversion, Genetics, Cerebral Cortex, agyria, clinical article, Extracellular Matrix Proteins, biology, Mental Disorders, Homozygote, Serine Endopeptidases, article, Brain, Pachygyria, Human brain, DAB1, Magnetic Resonance Imaging, Hypoplasia, Pedigree, Malformation of cortical development, Psychiatry and Mental health, medicine.anatomical_structure, Phenotype, priority journal, cerebellum hypoplasia, Female, point mutation, Chromosomes, Human, Pair 7, Inversion, Chromosome, Heterozygote, Cerebellar hypoplasia, gene locus, Cell Adhesion Molecules, Neuronal, Lissencephaly, Nerve Tissue Proteins, Cellular and Molecular Neuroscience, Cytogenetics, chromosome 7, medicine, Humans, human, gene, medicine.disease, Reelin Protein, nervous system, Chromosome Inversion, biology.protein, reln gene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d94be8c2432aa61f30526141dd1de85c
https://pubmed.ncbi.nlm.nih.gov/16958033