المؤلفون: Desiderio, Simon, Schwaller, Fred, Tartour, Kevin, Padmanabhan, Kiran, Lewin, Gary R, Carroll, Patrick, Marmigere, Frederic

المصدر: eLife, 12

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Animals, Mice, Gene Expression Regulation, Mechanoreceptors, Nervous System Physiological Phenomena, Sensory Receptor Cells, Transcription Factors -- genetics, Homeodomain Proteins -- genetics, Meis2, TALE homeodomain, chicken, developmental biology, dorsal root ganglion, mouse, neuroscience, sensory neurons, transcription factor

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

العلاقة: uri/info:doi/10.7554/eLife.89287; uri/info:pii/89287; uri/info:pmid/38386003; uri/info:pmcid/PMC10942617; https://dipot.ulb.ac.be/dspace/bitstream/2013/370554/3/elife-89287-v1.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/370554Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/370554Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/370554/3/elife-89287-v1.pdfTest

المؤلفون: Seiersen, Kasper V, Henriksen, Tine B, Andelius, Ted C K, Andreasen, Lotte, Diemer, Tue, Gudmundsdottir, Gudrun, Vogel, Ida, Gjørup, Vibike, Gregersen, Pernille A

المصدر: Seiersen , K V , Henriksen , T B , Andelius , T C K , Andreasen , L , Diemer , T , Gudmundsdottir , G , Vogel , I , Gjørup , V & Gregersen , P A 2024 , ' Combined achondroplasia and short stature homeobox-containing ( SHOX ) gene deletion in a Danish infant ' , European Journal of Medical Genetics , vol. 67 , 104894 . https://doi.org/10.1016/j.ejmg.2023.104894Test

مصطلحات موضوعية: Achondroplasia, FGFR3, Infant, SHOX, Short stature homeobox protein, Growth Disorders/genetics, Humans, Osteochondrodysplasias/genetics, Achondroplasia/genetics, Gene Deletion, Homeodomain Proteins/genetics, Denmark, Female, Short Stature Homeobox Protein/genetics, Genes, Homeobox

العلاقة: https://pure.au.dk/portal/en/publications/72ad996c-dec7-4880-9a2d-b6e30e24f2c7Test

الإتاحة: https://doi.org/10.1016/j.ejmg.2023.104894Test
https://pure.au.dk/portal/en/publications/72ad996c-dec7-4880-9a2d-b6e30e24f2c7Test
http://www.scopus.com/inward/record.url?scp=85179931911&partnerID=8YFLogxKTest

المؤلفون: Birnie, Anthony, Plat, Audrey, Korkmaz, Cemil, Bothma, Jacques P

المصدر: Birnie , A , Plat , A , Korkmaz , C & Bothma , J P 2023 , ' Precisely timed regulation of enhancer activity defines the binary expression pattern of Fushi tarazu in the Drosophila embryo ' , Current Biology , vol. 33 , no. 14 , pp. 2839-2850.e7 . https://doi.org/10.1016/j.cub.2023.04.005Test

مصطلحات موضوعية: Animals, Drosophila melanogaster/embryology, Drosophila Proteins/genetics, Enhancer Elements, Genetic, Gene Expression Regulation, Homeodomain Proteins/genetics, Transcription Factors/genetics

العلاقة: https://pure.knaw.nl/portal/en/publications/6a930b72-716e-4caa-b55b-431ac7ed2042Test

الإتاحة: https://doi.org/10.1016/j.cub.2023.04.005Test
https://doi.org/20.500.11755/6a930b72-716e-4caa-b55b-431ac7ed2042Test
https://pure.knaw.nl/portal/en/publications/6a930b72-716e-4caa-b55b-431ac7ed2042Test
https://hdl.handle.net/20.500.11755/6a930b72-716e-4caa-b55b-431ac7ed2042Test

المؤلفون: Baßler, Kevin, Schmidleithner, Lisa, Neubauer, Anna, Sakaguchi, Shimon, Barry, Simon C, Huehn, Jochen, Bonaguro, Lorenzo, Ulas, Thomas, Beyer, Marc-Daniel, Hadaddzadeh Shakiba, Mehrnoush, Elmzzahi, Tarek, Köhne, Maren, Floess, Stefan, Scholz, Rebekka, Ohkura, Naganari, Sadlon, Timothy, Klee, Kathrin

المصدر: Frontiers in immunology 14, 1107397 (2023). doi:10.3389/fimmu.2023.1107397

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Humans, T-Lymphocytes, Regulatory, Gene Expression Regulation, Gene Regulatory Networks, Forkhead Transcription Factors: genetics, Forkhead Transcription Factors: metabolism, Transcription Factors: metabolism, Homeodomain Proteins: genetics, Forkhead Transcription Factors, Foxp3, MEOX1, Treg cells, human CD4, regulatory T cells, FOXP3 protein, human, MEOX1 protein, Transcription Factors, Homeodomain Proteins

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1664-3224; info:eu-repo/semantics/altIdentifier/pmid/pmid:37559728; https://pub.dzne.de/record/259713Test; https://pub.dzne.de/search?p=id:%22DZNE-2023-00785%22Test

الإتاحة: https://doi.org/10.3389/fimmu.2023.1107397Test
https://pub.dzne.de/record/259713Test
https://pub.dzne.de/search?p=id:%22DZNE-2023-00785%22Test

المؤلفون: Oppermann, Henry, Marcos-Grañeda, Elia, Weiss, Linnea A, Gurnett, Christina A, Jelsig, Anne Marie, Vineke, Susanne H, Isidor, Bertrand, Mercier, Sandra, Magnussen, Kari, Zacher, Pia, Hashim, Mona, Pagnamenta, Alistair T, Race, Simone, Srivastava, Siddharth, Frazier, Zoë, Maiwald, Robert, Pergande, Matthias, Milani, Donatella, Rinelli, Martina, Levy, Jonathan, Krey, Ilona, Fontana, Paolo, Lonardo, Fortunato, Riley, Stephanie, Kretzer, Jasmine, Rankin, Julia, Reis, Linda M, Semina, Elena V, Reuter, Miriam S, Scherer, Stephen W, Iascone, Maria, Weis, Denisa, Fagerberg, Christina R, Brasch-Andersen, Charlotte, Hansen, Lars Kjaersgaard, Kuechler, Alma, Noble, Nathan, Gardham, Alice, Tenney, Jessica, Rathore, Geetanjali, Beck-Woedl, Stefanie, Haack, Tobias B, Pavlidou, Despoina C, Atallah, Isis, Vodopiutz, Julia, Janecke, Andreas R, Hsieh, Tzung-Chien, Lesmann, Hellen, Klinkhammer, Hannah, Krawitz, Peter M, Lemke, Johannes R, Jamra, Rami Abou, Nieto, Marta, Tümer, Zeynep, Platzer, Konrad

المصدر: Oppermann , H , Marcos-Grañeda , E , Weiss , L A , Gurnett , C A , Jelsig , A M , Vineke , S H , Isidor , B , Mercier , S , Magnussen , K , Zacher , P , Hashim , M , Pagnamenta , A T , Race , S , Srivastava , S , Frazier , Z , Maiwald , R , Pergande , M , Milani , D , Rinelli , M , Levy , J , Krey , I , Fontana , P , Lonardo , F , Riley , ....

مصطلحات موضوعية: Adult, Animals, Humans, Mice, Heterozygote, Homeodomain Proteins/genetics, Intellectual Disability/genetics, Neurodevelopmental Disorders/genetics, Phenotype, Repressor Proteins/genetics, Seizures, Transcription Factors/genetics

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1038/s41431-023-01445-2Test
https://curis.ku.dk/portal/da/publications/cux1related-neurodevelopmental-disorderTest(3d7eab98-3600-4715-b091-3ca1c635767c).html
https://curis.ku.dk/ws/files/387700368/s41431_023_01445_2.pdfTest

المساهمون: Oh-Seok Kwon, Myunghee Hong, Tae-Hoon Kim, Inseok Hwang, Jaemin Shim, Eue-Keun Choi, Hong Euy Lim, Hee Tae Yu, Jae-Sun Uhm, Boyoung Joung, Seil Oh, Moon-Hyoung Lee, Young-Hoon Kim, Hui-Nam Pak, Kim, Tae-Hoon

مصطلحات موضوعية: Artificial Intelligence, Atrial Fibrillation / diagnosis, Atrial Fibrillation / epidemiology, Atrial Fibrillation / genetics, DNA / genetics, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Homeodomain Proteins / genetics, Homeodomain Proteins / metabolism, Humans, Male, Middle Aged, Morbidity / trends, Polymorphism, Single Nucleotide, Republic of Korea / epidemiology, Transcription Factors / genetics, Transcription Factors / metabolism, atrial fibrillation, genetics

وصف الملف: application/pdf

العلاقة: OPEN HEART; J04205; OAK-2022-01428; https://ir.ymlib.yonsei.ac.kr/handle/22282913/188710Test; T202201859; OPEN HEART, Vol.9(1) : e001898, 2022-01

الإتاحة: https://doi.org/10.1136/openhrt-2021-001898Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188710Test

المؤلفون: El Fersioui, Y., Pinton, G., Allaman-Pillet, N., Schorderet, D.F.

المصدر: Cells, vol. 11, no. 7, pp. 1088

مصطلحات موضوعية: Animals, Eye Abnormalities/genetics, Genes, Homeobox, Homeodomain Proteins/genetics, Homeodomain Proteins/metabolism, Zebrafish/genetics, Zebrafish/metabolism, Zebrafish Proteins/genetics, Zebrafish Proteins/metabolism, bmp2b, bmp4, bone, chordin, noggin1, vertebrae, zebrafish

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35406651; info:eu-repo/semantics/altIdentifier/eissn/2073-4409; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_ABFAD8F72B593; https://serval.unil.ch/notice/serval:BIB_ABFAD8F72B59Test; urn:issn:2073-4409; https://serval.unil.ch/resource/serval:BIB_ABFAD8F72B59.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_ABFAD8F72B593Test

الإتاحة: https://doi.org/10.3390/cells11071088Test
https://serval.unil.ch/notice/serval:BIB_ABFAD8F72B59Test
https://serval.unil.ch/resource/serval:BIB_ABFAD8F72B59.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_ABFAD8F72B593Test

المؤلفون: Feifei, Liu, Richter, Anna, Runge, Jens, Keiler, Jonas, Hermann, Andreas, Kipp, Markus, Joost, Sarah

المصدر: Journal of molecular neuroscience 72(8), 1646-1655 (2022). doi:10.1007/s12031-022-02025-7

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Animals, Homeodomain Proteins: genetics, Mice, Paralysis: etiology, Precursor B-Cell Lymphoblastic Leukemia-Lymphoma: complications, X-Ray Microtomography, Hematologic Malignancy, Micro-CT, Paralysis, Pro B cell leukemia, RAG1-deficient mice

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0895-8696; info:eu-repo/semantics/altIdentifier/issn/1559-1166; info:eu-repo/semantics/altIdentifier/pmid/pmid:35583713; https://pub.dzne.de/record/164032Test; https://pub.dzne.de/search?p=id:%22DZNE-2022-00695%22Test

الإتاحة: https://doi.org/10.1007/s12031-022-02025-7Test
https://pub.dzne.de/record/164032Test
https://pub.dzne.de/search?p=id:%22DZNE-2022-00695%22Test

المؤلفون: Elsner, Jonas, Mensah, Martin A., Holtgrewe, Manuel, Hertzberg, Jakob, Bigoni, Stefania, Busche, Andreas, Coutelier, Marie, de Silva, Deepthi C., Elçioglu, Nursel, Filges, Isabel, Gerkes, Erica, Girisha, Katta M., Graul-Neumann, Luitgard, Jamsheer, Aleksander, Krawitz, Peter, Kurth, Ingo, Markus, Susanne, Megarbane, Andre, Reis, André, Reuter, Miriam S., Svoboda, Daniel, Teller, Christopher, Tuysuz, Beyhan, Türkmen, Seval, Wilson, Meredith, Woitschach, Rixa, Vater, Inga, Caliebe, Almuth, Hülsemann, Wiebke, Horn, Denise, Mundlos, Stefan, Spielmann, Malte

المصدر: http://lobid.org/resources/99370671251406441Test#!, 140(8):1229-1239.

مصطلحات موضوعية: Transcription Factors/genetics [MeSH], Limb Deformities, Congenital/metabolism [MeSH], Molecular Medicine, Gene Expression [MeSH], Cohort Studies [MeSH], Genetic Testing [MeSH], Original Investigation, Congenital/pathology [MeSH], Infant [MeSH], Male [MeSH], Base Sequence [MeSH], Human Genetics, Transcription Factors/deficiency [MeSH], Mutation [MeSH], Whole Genome Sequencing [MeSH], Humans [MeSH], Genetic Heterogeneity [MeSH], Homeodomain Proteins/genetics [MeSH], DNA Copy Number Variations [MeSH], Pedigree [MeSH], Metabolic Diseases, Ubiquitin-Activating Enzymes/deficiency [MeSH], Gene Function, Ubiquitin-Activating Enzymes/genetics [MeSH], Congenital/genetics [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6446834Test; https://doi.org/10.1007/s00439-021-02295-yTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263393Test/

الإتاحة: https://doi.org/10.1007/s00439-021-02295-yTest
https://repository.publisso.de/resource/frl:6446834Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263393Test/

المؤلفون: Jiang, Dongsheng, Rinkevich, Yuval

المصدر: http://lobid.org/resources/99370677347406441Test#!, 6(1):332.

مصطلحات موضوعية: Research Highlight, Wound Healing/genetics [MeSH], Fibroblasts/cytology [MeSH], Humans [MeSH], Developmental biology, Homeodomain Proteins/genetics [MeSH], Cell Differentiation/genetics [MeSH], Animals [MeSH], Physiology, Mice [MeSH], Cicatrix/genetics [MeSH], Cell biology, Mammals/genetics [MeSH], Cicatrix/pathology [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6442596Test; https://doi.org/10.1038/s41392-021-00738-6Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410910Test/

الإتاحة: https://doi.org/10.1038/s41392-021-00738-6Test
https://repository.publisso.de/resource/frl:6442596Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410910Test/