المؤلفون: Nordström, Ulrika, 1971, Maier, Esther, 1974, Jessell, Thomas M, Edlund, Thomas

المصدر: PLoS biology. 4(8):1438-1452

مصطلحات موضوعية: Animals, Avian Proteins/genetics/metabolism, Central Nervous System/*embryology, Chick Embryo, Fibroblast Growth Factors/metabolism, Gene Expression Regulation, Developmental, Genes, Homeobox, Homeodomain Proteins/genetics/*metabolism, Motor Neurons/*cytology/metabolism, Rhombencephalon/cytology/embryology/metabolism, Signal Transduction, Spinal Cord/cytology/embryology/metabolism, Stem Cells/cytology/metabolism, T-Box Domain Proteins/genetics/metabolism, Tretinoin/metabolism, Wnt Proteins/genetics/*metabolism

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-5811Test
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16895440&dopt=CitationTest
https://umu.diva-portal.org/smash/get/diva2:145479/FULLTEXT01.pdfTest

المؤلفون: Sauvegarde, Caroline, Paul, Delphine, Bridoux, Laure, Jouneau, Alice, Degrelle, Séverine, Hue, Isabelle, Rezsohazy, René, Donnay, Isabelle

المصدر: PloS one, 11 (10

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Animals, Blastocyst -- metabolism, Cattle, Cell Lineage -- genetics, Embryonic Development -- genetics, Endoderm -- metabolism, Fetus, Fluorescent Antibody Technique, Gastrulation -- genetics, Gene Expression, Gene Knockout Techniques, Homeodomain Proteins -- genetics -- metabolism, Humans, Immunohistochemistry, Mammals, Mice, Oocytes -- metabolism, Oogenesis -- genetics, Protein Transport, Zygote -- metabolism

وصف الملف: 1 full-text file(s): application/pdf

العلاقة: uri/info:doi/10.1371/journal.pone.0165898; uri/info:pii/PONE-D-16-26268; uri/info:pmid/27798681; uri/info:pmcid/PMC5087947; https://dipot.ulb.ac.be/dspace/bitstream/2013/351974/1/doi_335618.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/351974Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/351974Test

المؤلفون: Ba, Ibrahima, Cuccuini, Wendy, Clappier, Emmanuelle

المساهمون: Hematology Laboratory, APHP, Hôpital Saint-Louis, Paris, France

مصطلحات موضوعية: LL-B, CUX1, NUTM, translocation, Leukaemia Section, Animals, Carcinogenesis/genetics, DNA Copy Number Variations, Gene Expression, Genes, Tumor Suppressor, Genetic Predisposition to Disease, Haploinsufficiency, Homeodomain Proteins/*genetics/metabolism, Humans, Mutation, Neoplasms/*genetics/metabolism/pathology, Nuclear Proteins/*genetics/metabolism, Repressor Proteins/*genetics/metabolism, Acute Disease, Blotting, Western, Cell Line, Tumor, Chromosome Deletion, Chromosomes, Human, Pair 7/*genetics, Drosophila melanogaster/genetics, Gene Expression Profiling

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0715q22q14ID1272.htmlTest; Ibrahima, Ba; Wendy, Cuccuini; Emmanuelle, Clappier. t(7;15)(q22;q14) CUX1/NUTM1 a novel fusion. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 9, p. 491-493; http://hdl.handle.net/2042/66073Test; https://doi.org/10.4267/2042/66073Test

الإتاحة: https://doi.org/10.4267/2042/66073Test
http://hdl.handle.net/2042/66073Test

المؤلفون: Li, Carman Man-Chung, Jacks, Tyler

المساهمون: David H. Koch Institute for Integrative Cancer Research, Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA

مصطلحات موضوعية: SH3PXD2A, TKS5, podosomes, invadopodia, metastasis, Genes Section, Adenocarcinoma/genetics/mortality/*physiopathology, Animals, Genetically Modified, CDX2 Transcription Factor, Cell Line, Tumor, Gene Expression Regulation, Neoplastic/genetics, Gene Knockdown Techniques, Gene Silencing, Hepatocyte Nuclear Factor 3-beta/genetics/*metabolism, Homeodomain Proteins/genetics/*metabolism

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Genes/SH3PXD2AID45995ch10q24.htmlTest; Carman Man-Chung, Li; Tyler, Jacks. SH3PXD2A (SH3 and PX domains 2A). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 6, p. 326-330; http://hdl.handle.net/2042/62941Test; https://doi.org/10.4267/2042/62941Test

الإتاحة: https://doi.org/10.4267/2042/62941Test
http://hdl.handle.net/2042/62941Test

المؤلفون: Chen, Anna, Wong, Christina, Liu, Mira, House, Colin, Sceneay, Jaclyn, Bowtell, David, Thompson, Rik, Moller, Andrea

المصدر: OncoTarget

مصطلحات موضوعية: Gene Expression Regulation, Animals, Blotting, Breast Neoplasms/genetics/metabolism/pathology, Cell Line, Epithelial-Mesenchymal Transition/drug effects/*genetics, Female, Fluorescence, Gene Expression Profiling, Genetic, Homeodomain Proteins/*genetics/metabolism, Humans, MCF-7 Cells, Mice, Microscopy, Models, Neoplastic, Nuclear Proteins/*genetics/metabolism, RNA Interference, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction/drug effects/genetics, Transcription Factors/*genetics/metabolism, Transforming Growth Factor alpha/pharmacology, Transforming Growth Factor beta/pharmacology, Tumor, Ubiquitin-Protein Ligases/*genetics/metabolism, Western

وصف الملف: application/pdf

العلاقة: https://eprints.qut.edu.au/97702/1/97702.pdfTest; Chen, Anna, Wong, Christina, Liu, Mira, House, Colin, Sceneay, Jaclyn, Bowtell, David, Thompson, Rik, & Moller, Andrea (2015) The ubiquitin ligase Siah is a novel regulator of Zeb1 in breast cancer. OncoTarget, 6(2), pp. 862-873.; https://eprints.qut.edu.au/97702Test/; Faculty of Health; Institute of Health and Biomedical Innovation

الإتاحة: https://doi.org/10.18632/oncotarget.2696Test
https://eprints.qut.edu.au/97702Test/

المؤلفون: Chaumeil, Julie, Micsinai, Mariann, Ntziachristos, Panagiotis, Deriano, Ludovic, Wang, Joy M-H, Ji, Yanhong, Nora, Elphege P, Rodesch, Matthew J, Jeddeloh, Jeffrey A, Aifantis, Iannis, Kluger, Yuval, Schatz, David G, Skok, Jane A

المساهمون: New York University School of Medicine (NYU), New York University School of Medicine, NYU System (NYU)-NYU System (NYU), Développement lymphocytaire et Oncogénèse, Institut Pasteur Paris (IP)-Centre National de la Recherche Scientifique (CNRS), Génétique et Biologie du Développement, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Curie Paris -Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Roche NimbleGen Inc., Yale Cancer Center, Yale School of Medicine New Haven, Connecticut (YSM), Yale University New Haven, Howard Hughes Medical Institute (HHMI), This work is supported by the National Institute ofHealth: R01GM086852 (to J.A.S.), R37AI32524 (to D.G.S.), RO1CA133379,RO1CA105129, RO1CA149655, and RO1GM088847 (to I.A.). J.A.S. is aLeukemia & Lymphoma Society (LLS) scholar. J.C. is an Irvington Institute Fellow of the Cancer Research Institute. M.M. was supported by an NSFIGERT 0333389. L.D. was an LLS Fellow. E.P.N. was supported by the FrenchMinistry of Research and the Association pour la Recherche sur le Cancer(France). I.A. is also supported by the Leukemia & Lymphoma Society (TRPgrant), The V Foundation for Cancer Research, and the Dana Foundation.D.G.S. is an Investigator, and I.A. is an Early Career Scientist of the HowardHughes Medical Institute. The authors from Roche NimbleGen, Inc. (M.J.R.and J.A.J.) recognize a competing interest in this publication as employeesof the company.

المصدر: ISSN: 2211-1247.

مصطلحات موضوعية: V(D)J Recombination, Alleles, Animals, Ataxia Telangiectasia Mutated Proteins, Cell Cycle Proteins/metabolism, Cell Nucleus/metabolism, DNA-Binding Proteins/genetics/*metabolism, DNA Damage, Genetic Loci, Genomic Instability, Histones/genetics, Homeodomain Proteins/genetics/*metabolism, Mice, Inbred C57BL, Inbred CBA, Knockout, Protein-Serine-Threonine Kinases/metabolism, Receptors, Antigen, T-Cell, alpha-beta/genetics/*metabolism, Tumor Suppressor Proteins/metabolism, MESH: Alleles, MESH: Animals, MESH: V(D)J Recombination, MESH: Ataxia Telangiectasia Mutated Proteins, MESH: Cell Cycle Proteins, MESH: Cell Nucleus, MESH: DNA Damage, MESH: DNA-Binding Proteins

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23416051; pasteur-01471693; https://pasteur.hal.science/pasteur-01471693Test; https://pasteur.hal.science/pasteur-01471693/documentTest; https://pasteur.hal.science/pasteur-01471693/file/1-s2.0-S2211124713000314-main.pdfTest; PUBMED: 23416051; PUBMEDCENTRAL: PMC3664546

الإتاحة: https://doi.org/10.1016/j.celrep.2013.01.024Test
https://pasteur.hal.science/pasteur-01471693Test
https://pasteur.hal.science/pasteur-01471693/documentTest
https://pasteur.hal.science/pasteur-01471693/file/1-s2.0-S2211124713000314-main.pdfTest

المؤلفون: SaePang, JJ, Ling, KW, Sham, MH, Mak, SS, Wong, EYM, Fritzsch, B, Wang, XA

مصطلحات موضوعية: Posterior prevalence, Hoxb3, Neurogenesis, Neuronal identity, Rhombomere 4, Hindbrain patterning, Hox gene regulation, Hoxb1, Facial branchiomotor neurons, Homeodomain Proteins - Genetics - Metabolism, Animals, Genetically Modified, Avian Proteins - Genetics - Metabolism, Base Sequence, Binding Sites - Genetics, Body Patterning, Gene Expression Regulation, Developmental, Chick Embryo, Craniofacial Abnormalities - Embryology - Genetics - Metabolism, Dna Primers - Genetics, Mice, Mutant Strains, Transgenic, Models, Neurological, Neurogenesis - Genetics - Physiology, Rhombencephalon - Embryology - Metabolism

العلاقة: Developmental Biology; http://www.scopus.com/mlt/select.url?eid=2-s2.0-79953025098&selection=ref&src=s&origin=recordpageTest; Developmental Biology, 2011, v. 352 n. 2, p. 382-392; 8836299; 392; 190257; WOS:000289180200018; eid_2-s2.0-79953025098; 382; http://hdl.handle.net/10722/147630Test; 352

الإتاحة: https://doi.org/10.1016/j.ydbio.2011.02.003Test
http://hdl.handle.net/10722/147630Test

المؤلفون: GarciaBarcelo, MM, Tam, PKH, Zhu, J, Lui, VCH

مصطلحات موضوعية: Homeodomain Proteins - genetics - metabolism, Transcription, Genetic, Transcription Factors - genetics - metabolism, Proto-Oncogene Proteins c-ret - genetics - metabolism, Nuclear Proteins - genetics - metabolism

العلاقة: PLoS ONE; http://www.scopus.com/mlt/select.url?eid=2-s2.0-79958046096&selection=ref&src=s&origin=recordpageTest; Plos One, 2011, v. 6 n. 6; e20815; 187594; WOS:000291355500045; PMC3108997; eid_2-s2.0-79958046096; http://hdl.handle.net/10722/135531Test

الإتاحة: https://doi.org/10.1371/journal.pone.0020815Test
http://hdl.handle.net/10722/135531Test

المؤلفون: Lam, CSC, Wong, BCY, Hung, IF, Tan, VPY, Pang, R, Wang, JD, Wang, QY, Lan, HY, Chen, MH, Zou, B, Chen, WJ, Ma, J, Zhang, WJ

مصطلحات موضوعية: Homeodomain Proteins - genetics - metabolism, DNA Methylation, Gene Silencing, Trans-Activators - genetics - metabolism, Stomach Neoplasms - genetics

العلاقة: Carcinogenesis; http://www.scopus.com/mlt/select.url?eid=2-s2.0-77956290718&selection=ref&src=s&origin=recordpageTest; Carcinogenesis, 2010, v. 31 n. 9, p. 1552-1560; 7842378; 1560; 174515; WOS:000281530400007; http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0143-3334&volume=31&issue=9&spage=1552&epage=1560&date=2010&atitle=Promoter+hypermethylation+and+histone+hypoacetylation+contribute+to+Pancreatic-duodenal+homeobox+1Test+(PDX1)+silencing+in+gastric+cancer; eid_2-s2.0-77956290718; 1552; http://hdl.handle.net/10722/124948Test; 31

الإتاحة: https://doi.org/10.1093/carcin/bgq140Test
http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0143-3334&volume=31&issue=9&spage=1552&epage=1560&date=2010&atitle=Promoter+hypermethylation+and+histone+hypoacetylation+contribute+to+Pancreatic-duodenal+homeobox+1Test+(PDX1)+silencing+in+gastric+cancer
http://hdl.handle.net/10722/124948Test

المؤلفون: GarciaBarcelo, MM, Ngan, ESW, Tam, PKH, So, MT, Leon, TYY, Poon, HC, Lui, VCH

مصطلحات موضوعية: Nkx2-1, Transcription, RET, Phox2b, Hirschsprung Disease - genetics, Enteric Nervous System - metabolism, Transcription Factors - genetics - metabolism, Proto-Oncogene Proteins c-ret - genetics - metabolism, Homeodomain Proteins - genetics - metabolism

العلاقة: Journal of Pediatric Surgery; http://www.scopus.com/mlt/select.url?eid=2-s2.0-70350070157&selection=ref&src=s&origin=recordpageTest; Journal Of Pediatric Surgery, 2009, v. 44 n. 10, p. 1904-1912; 1912; 167940; WOS:000271331700006; 10; http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-3468&volume=44&issue=10&spage=1904&epage=1912&date=2009&atitle=Transcriptional+regulation+of+RET+by+Nkx2-1,+Phox2b,+Sox10,+and+Pax3Test; eid_2-s2.0-70350070157; 1904; http://hdl.handle.net/10722/83692Test; 44

الإتاحة: https://doi.org/10.1016/j.jpedsurg.2008.11.055Test
http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-3468&volume=44&issue=10&spage=1904&epage=1912&date=2009&atitle=Transcriptional+regulation+of+RET+by+Nkx2-1,+Phox2b,+Sox10,+and+Pax3Test
http://hdl.handle.net/10722/83692Test