المساهمون: Dong Suk Yoon, Yun Hee Kim, Seulgi Lee, Kyoung-Mi Lee, Kwang Hwan Park, Yeonsue Jang, Jin Woo Lee, Park, Kwang Hwan, Yoon, Dong Suk, Lee, Kyung Mi, Lee, Seul Gi, Lee, Jin Woo, Jang, Yeon Sue, Lee, Kyoung Mi

مصطلحات موضوعية: Adult, Bone Marrow/metabolism, Cell Communication/genetics, Cell Differentiation/genetics, Cell Lineage/genetics, Cellular Senescence/genetics, Core Binding Factor Alpha 1 Subunit/genetics, Core Binding Factor Alpha 1 Subunit/metabolism, Cytokines/genetics, Cytokines/metabolism, Down-Regulation/genetics, Female, Homeodomain Proteins/genetics, Homeodomain Proteins/metabolism, Humans, Interleukin-6/genetics, Interleukin-6/metabolism, Male, Middle Aged, Multipotent Stem Cells/metabolism, Osteogenesis/genetics, SOXB1 Transcription Factors/genetics, SOXB1 Transcription Factors/metabolism, Transcription Factors/genetics, Transcription Factors/metabolism, Transcription, Genetic/genetics, Up-Regulation/genetics, Young Adult, Dlx5

وصف الملف: 3273~3286

العلاقة: FASEB JOURNAL; J00889; OAK-2014-01129; https://ir.ymlib.yonsei.ac.kr/handle/22282913/99049Test; http://www.fasebj.org/content/28/7/3273.longTest; T201402011; FASEB JOURNAL, Vol.28(7) : 3273-3286, 2014

الإتاحة: https://doi.org/10.1096/fj.13-248567Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/99049Test
http://www.fasebj.org/content/28/7/3273.longTest

المؤلفون: Isabelle Stévant, Julien Prados, Emmanouil T. Dermitzakis, Serge Nef, Subashika Govindan, Denis Jabaudon, Alexandre Dayer, Ludovic Telley

المصدر: Science, Vol. 351, No 6280 (2016) pp. 1443-1446

مصطلحات موضوعية: Male, 0301 basic medicine, Transcription, Genetic, Cerebral Ventricles/cytology/embryology, Neocortex, Bioinformatics, Green Fluorescent Proteins/genetics, Cerebral Ventricles, Transcriptome, ddc:616.89, Mice, Neurons/cytology, 0302 clinical medicine, Neural Stem Cells, Basic Helix-Loop-Helix Transcription Factors, Nerve Tissue Proteins/genetics, ddc:576.5, Neurons, Neuropeptides/genetics, Multidisciplinary, Neurogenesis, Neural stem cell, DNA-Binding Proteins, Corticogenesis, medicine.anatomical_structure, Excitatory postsynaptic potential, Female, Green Fluorescent Proteins, Nerve Tissue Proteins, GPI-Linked Proteins/genetics, Biology, GPI-Linked Proteins, 03 medical and health sciences, medicine, Animals, Progenitor cell, Progenitor, Basic Helix-Loop-Helix Transcription Factors/genetics, SOXB1 Transcription Factors, Neuropeptides, Neural Stem Cells/cytology, Neocortex/cytology/embryology, ddc:616.8, 030104 developmental biology, nervous system, SOXB1 Transcription Factors/genetics, Neurogenesis/genetics, T-Box Domain Proteins, Neuroscience, DNA-Binding Proteins/genetics, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1c405c6d3bfeb5df303927aa0dee512Test
https://doi.org/10.1126/science.aad8361Test

المؤلفون: Telley, Ludovic, Govindan, Subashika, Prados, Julien, Stevant, Isabelle, Nef, Serge, Dermitzakis, Emmanouil, Dayer, Alexandre, Jabaudon, Denis

المصدر: ISSN: 0036-8075 ; Science, vol. 351, no. 6280 (2016) p. 1443-1446.

مصطلحات موضوعية: info:eu-repo/classification/ddc/576.5, info:eu-repo/classification/ddc/616.8, info:eu-repo/classification/ddc/616.89, Animals, Basic Helix-Loop-Helix Transcription Factors/genetics, Cerebral Ventricles/cytology/embryology, DNA-Binding Proteins/genetics, Female, GPI-Linked Proteins/genetics, Green Fluorescent Proteins/genetics, Male, Mice, Neocortex/cytology/embryology, Nerve Tissue Proteins/genetics, Neural Stem Cells/cytology, Neurogenesis/genetics, Neurons/cytology, Neuropeptides/genetics, SOXB1 Transcription Factors/genetics, Transcription, Genetic, Transcriptome

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26940868; https://archive-ouverte.unige.ch/unige:86827Test; unige:86827

الإتاحة: https://doi.org/10.1126/science.aad8361Test
https://archive-ouverte.unige.ch/unige:86827Test

المؤلفون: Chassaing, N., Causse, A., Vigouroux, A., Delahayes, A., Alessandri, J.-L., Boespflug-Tanguy, O., Boute-Benejean, O., Dollfus, H., Duban-Bedu, B., Gilbert-Dussardier, B., Giuliano, F., Gonzales, M., Holder-Espinasse, M., Isidor, B., Jacquemont, M.-L., Lacombe, D., Martin-Coignard, D., Mathieu-Dramard, M., Odent, S., Picone, O., Pinson, L., Quelin, C., Sigaudy, Sabine, Toutain, A., Thauvin-Robinet, C., Kaplan, Josseline, Calvas, Patrick

المساهمون: CHU Toulouse [Toulouse], Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées, UFR Santé, Médecine et Biologie Humaine (UFR SMBH), Université Sorbonne Paris Nord, Physiopathologie et neuroprotection des atteintes du cerveau en développement, Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Universitaire de La Réunion (CHU La Réunion), AP-HP Hôpital universitaire Robert-Debré [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Service de génétique médicale, CHU Strasbourg-Hôpital de Hautepierre [Strasbourg], Groupe Hospitalier de l'Institut Catholique de Lille (GHICL), Hôpital de la Milétrie, Centre hospitalier universitaire de Poitiers (CHU Poitiers), Hôpital Archet 2 [Nice] (CHU), Universidad Politécnica de Madrid (UPM), CHU Trousseau [APHP], Université Pierre et Marie Curie - Paris 6 - UFR de Médecine Pierre et Marie Curie (UPMC), Université Pierre et Marie Curie - Paris 6 (UPMC), Centre hospitalier universitaire de Nantes (CHU Nantes), CHU Bordeaux [Bordeaux], Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) (U1211 INSERM/MRGM), Université de Bordeaux (UB)-Groupe hospitalier Pellegrin-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Le Mans (CH Le Mans), CHU Amiens-Picardie, Centre Hospitalier Universitaire [Rennes], Hôpital de la Timone [CHU - APHM] (TIMONE), Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut National de l'Environnement Industriel et des Risques (INERIS), Faculté des Sciences Pharmaceutiques et Biologiques / Laboratoire d'Hygiène et de Santé Publique, Université Paris Descartes - Paris 5 (UPD5), Génie des procédés frigorifiques (UR GPAN), Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA), Service de génétique clinique, Hôpital Jeanne de Flandre [Lille]-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Production du lait (PL), Institut National de la Recherche Agronomique (INRA)-AGROCAMPUS OUEST, Service de Génétique et de Diagnostic Prénatal, Université de la Méditerranée - Aix-Marseille 2, CHU Toulouse [Toulouse]-Hôpital Purpan [Toulouse], Université catholique de Lille (UCL), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Université de Toulouse (UT), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Institut National de l'Environnement Industriel et des Risques ( INERIS ), Université Paris Descartes - Paris 5 ( UPD5 ), Génie des procédés frigorifiques ( UR GPAN ), Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture ( IRSTEA ), Universidad Politécnica de Madrid ( UPM ), Hôpital Jeanne de Flandre [Lille]-Centre Hospitalier Régional Universitaire [Lille] ( CHRU Lille ), Production du lait ( PL ), Institut National de la Recherche Agronomique ( INRA ) -AGROCAMPUS OUEST, Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand ( CHU Dijon ), Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement ( Inserm U781 ), Université Paris Descartes - Paris 5 ( UPD5 ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)

المصدر: Clinical Genetics
Clinical Genetics, Wiley, 2014, 86 (4), pp.326-334. ⟨10.1111/cge.12275⟩
Clinical Genetics, Wiley, 2014, 86 (4), pp.326--334. ⟨10.1111/cge.12275⟩
Clinical Genetics, 2014, 86 (4), pp.326-334. ⟨10.1111/cge.12275⟩
Clinical Genetics, Wiley, 2014, 86 (4), pp.326--334. 〈10.1111/cge.12275〉

مصطلحات موضوعية: Male, PAX6 Transcription Factor, RAX, [SDV]Life Sciences [q-bio], SOX2, Growth Differentiation Factor 6, anophthalmia, MESH: Anophthalmos / genetics, MESH: Forkhead Transcription Factors / genetics, MESH: Child, Microphthalmos, Paired Box Transcription Factors, Child, MESH: Anophthalmos / pathology, MESH: Microphthalmos / pathology, Otx Transcription Factors, GDF6, MESH: Genetic Heterogeneity, Forkhead Transcription Factors, MESH: Infant, MESH: PAX6 Transcription Factor, Child, Preschool, Female, MESH: SOXB1 Transcription Factors / genetics, Adult, MESH: Otx Transcription Factors / genetics, Adolescent, MESH: Eye Proteins / genetics, MESH: Anophthalmos / diagnosis, MESH: Transcription Factors / genetics, MESH: Microphthalmos / diagnosis, Genetic Heterogeneity, MESH: Point Mutation / genetics, Humans, Point Mutation, VSX2, Eye Proteins, MESH: Homeodomain Proteins / genetics, Homeodomain Proteins, MESH: Adolescent, MESH: Humans, [ SDV ] Life Sciences [q-bio], SOXB1 Transcription Factors, MESH: Child, Preschool, MESH: Microphthalmos / genetics, Anophthalmos, Infant, MESH: Adult, MESH: Paired Box Transcription Factors / genetics, MESH: Growth Differentiation Factor 6 / genetics, eye diseases, MESH: Repressor Proteins / genetics, MESH: Male, PAX6, Repressor Proteins, microphthalmia, FOXE3, sense organs, MESH: Female, Transcription Factors, OTX2

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4aacf8c5d4d2e23e38ea8b0dc8884cb8Test
https://hal.archives-ouvertes.fr/hal-01064928Test

المؤلفون: Lan, Jie, Song, Hua, Yuan, Yuan, Zhan, Liping, Xiao-ning, He, Zhang, Yong

المصدر: Zygote, 19 (2

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Animals, Cattle, CpG Islands, DNA Methylation, Fibroblast Growth Factor 4 -- genetics, Germ Cells -- metabolism, Kruppel-Like Transcription Factors -- genetics, Male, Octamer Transcription Factor-3 -- genetics, Oocytes -- metabolism, Pluripotent Stem Cells -- metabolism, SOXB1 Transcription Factors -- genetics, Spermatozoa -- metabolism

وصف الملف: No full-text files

العلاقة: uri/info:doi/10.1017/S0967199410000262; uri/info:pii/S0967199410000262; uri/info:pmid/20604984; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/265934Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/265934Test

المؤلفون: Lan, Jie, Song, Hua, Zhang, Hailin, Song, Yongli, Liu, Jun, Zhang, Yong

المصدر: Journal of Genetics and Genomics, 37 (5

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Animals, Cattle -- embryology -- genetics -- metabolism, Cloning, Organism, DNA Methylation, Embryonic Development, Female, Fertilization in Vitro, Fibroblast Growth Factor 4 -- genetics -- metabolism, Homeodomain Proteins -- genetics -- metabolism, Male, Nuclear Transfer Techniques, Octamer Transcription Factor-3 -- genetics -- metabolism, SOXB1 Transcription Factors -- genetics -- metabolism

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

العلاقة: uri/info:doi/10.1016/S1673-8527(09)60047-3; uri/info:pii/S1673-8527(09)60047-3; uri/info:pmid/20513630; https://dipot.ulb.ac.be/dspace/bitstream/2013/265926/1/Elsevier_249553.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/265926Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/265926Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/265926/1/Elsevier_249553.pdfTest