المؤلفون: Sen, P., Yang, Y., Navarro, C., Silva, I., Szafranski, P., Kolodziejska, K.E., Dharmadhikari, A.V., Mostafa, H., Kozakewich, H., Kearney, D., Cahill, J.B., Whitt, M., Bilic, M., Margraf, L., Charles, A., Goldblatt, J., Gibson, K., Lantz, P.E., Garvin, A.J., Petty, J., Kiblawi, Z., Zuppan, C., McConkie-Rosell, A., McDonald, M.T., Peterson-Carmichael, S.L., Gaede, J.T., Shivanna, B., Schady, D., Friedlich, P.S., Hays, S.R., Palafoll, I.V., Siebers-Renelt, U., Bohring, A., Finn, L.S., Siebert, J.R., Galambos, C., Nguyen, L., Riley, M., Chassaing, N., Vigouroux, A., Rocha, G., Fernandes, S., Brumbaugh, J., Roberts, K., Ho-Ming, L., Lo, I.F., Lam, S., Gerychova, R., Jezova, M., Valaskova, I., Fellmann, F., Afshar, K., Giannoni, E., Muhlethaler, V., Liang, J., Beckmann, J.S., Lioy, J., Deshmukh, H., Srinivasan, L., Swarr, D.T., Sloman, M., Shaw-Smith, C., van Loon, R.L., Hagman, C., Sznajer, Y., Barrea, C., Galant, C., Detaille, T., Wambach, J.A., Cole, F.S., Hamvas, A., Prince, L.S., Diderich, K.E., Brooks, A.S., Verdijk, R.M., Ravindranathan, H., Sugo, E., Mowat, D., Baker, M.L., Langston, C., Welty, S., Stankiewicz, P.

المصدر: Human mutation, vol. 34, no. 6, pp. 801-811

مصطلحات موضوعية: Amino Acid Sequence, Chromosome Mapping, Databases, Genetic, Female, Forkhead Transcription Factors/chemistry, Forkhead Transcription Factors/genetics, Forkhead Transcription Factors/metabolism, Gene Dosage, Gene Order, Humans, Infant, Newborn, Male, Molecular Sequence Data, Mutation, Open Reading Frames, Persistent Fetal Circulation Syndrome/genetics, Persistent Fetal Circulation Syndrome/metabolism, Persistent Fetal Circulation Syndrome/mortality, Persistent Fetal Circulation Syndrome/pathology, Protein Interaction Domains and Motifs/genetics, Sequence Alignment

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/23505205; info:eu-repo/semantics/altIdentifier/eissn/1098-1004; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_FA8E13315D590; https://serval.unil.ch/notice/serval:BIB_FA8E13315D59; https://serval.unil.ch/resource/serval:BIB_FA8E13315D59.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_FA8E13315D59
https://doi.org/10.1002/humu.22313
https://serval.unil.ch/resource/serval:BIB_FA8E13315D59.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_FA8E13315D590

المؤلفون: Neilson, Karen M., Klein, Steven L., Mhaske, Pallavi, Mood, Kathy, Daar, Ira O., Moody, Sally A.

المصدر: Anatomy and Regenerative Biology Faculty Publications

مصطلحات موضوعية: Ectoderm--embryology, Forkhead Transcription Factors--chemistry, Neural Plate--embryology, Transcriptional Activation, Xenopus Proteins--chemistry, Anatomy

Relation: https://hsrc.himmelfarb.gwu.edu/smhs_anatregbio_facpubs/10; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679181/

الاتاحة: https://hsrc.himmelfarb.gwu.edu/smhs_anatregbio_facpubs/10
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679181/

المؤلفون: Roll, Patrice, Vernes, Sonja C, Bruneau, Nadine, Cillario, Jennifer, Ponsole-Lenfant, Magali, Massacrier, Annick, Rudolf, Gabrielle, Khalife, Manal, Hirsch, Edouard, Fisher, Simon E, Szepetowski, Pierre

المصدر: Roll , P , Vernes , S C , Bruneau , N , Cillario , J , Ponsole-Lenfant , M , Massacrier , A , Rudolf , G , Khalife , M , Hirsch , E , Fisher , S E & Szepetowski , P 2010 , ' Molecular networks implicated in speech-related disorders : FOXP2 regulates the SRPX2/uPAR complex ' , Human Molecular Genetics , vol. 19 , no. 24 , pp. 4848-60 . https://doi.org/10.1093/hmg/ddq415

مصطلحات موضوعية: Amino Acid Sequence, Base Sequence, Binding Sites, Consensus Sequence/genetics, Electrophoretic Mobility Shift Assay, Female, Forkhead Transcription Factors/chemistry, Gene Regulatory Networks, Genes, Reporter, HEK293 Cells, Humans, Luciferases/metabolism, Male, Malformations of Cortical Development/complications, Molecular Sequence Data, Mutation, Missense/genetics, Nerve Tissue Proteins/genetics, Pedigree, Promoter Regions, Genetic/genetics, Protein Binding, RNA, Messenger/genetics, Receptors, Urokinase Plasminogen Activator/genetics, Speech Disorders/complications

الاتاحة: https://risweb.st-andrews.ac.uk/portal/en/researchoutput/molecular-networks-implicated-in-speechrelated-disorders(c6dba9e1-9abe-480b-b80d-e515a6c69e71).html
https://doi.org/10.1093/hmg/ddq415

المؤلفون: Roll, Patrice, Vernes, Sonja C, Bruneau, Nadine, Cillario, Jennifer, Ponsole-Lenfant, Magali, Massacrier, Annick, Rudolf, Gabrielle, Khalife, Manal, Hirsch, Edouard, Fisher, Simon E, Szepetowski, Pierre

المصدر: Roll , P , Vernes , S C , Bruneau , N , Cillario , J , Ponsole-Lenfant , M , Massacrier , A , Rudolf , G , Khalife , M , Hirsch , E , Fisher , S E & Szepetowski , P 2010 , ' Molecular networks implicated in speech-related disorders : FOXP2 regulates the SRPX2/uPAR complex ' , Human Molecular Genetics , vol. 19 , no. 24 , pp. 4848-60 . https://doi.org/10.1093/hmg/ddq415

مصطلحات موضوعية: Amino Acid Sequence, Base Sequence, Binding Sites, Consensus Sequence/genetics, Electrophoretic Mobility Shift Assay, Female, Forkhead Transcription Factors/chemistry, Gene Regulatory Networks, Genes, Reporter, HEK293 Cells, Humans, Luciferases/metabolism, Male, Malformations of Cortical Development/complications, Molecular Sequence Data, Mutation, Missense/genetics, Nerve Tissue Proteins/genetics, Pedigree, Promoter Regions, Genetic/genetics, Protein Binding, RNA, Messenger/genetics, Receptors, Urokinase Plasminogen Activator/genetics, Speech Disorders/complications

الاتاحة: https://research-portal.st-andrews.ac.uk/en/publications/c6dba9e1-9abe-480b-b80d-e515a6c69e71
https://doi.org/10.1093/hmg/ddq415

المؤلفون: Roll, Patrice, Vernes, Sonja C, Bruneau, Nadine, Cillario, Jennifer, Ponsole-Lenfant, Magali, Massacrier, Annick, Rudolf, Gabrielle, Khalife, Manal, Hirsch, Edouard, Fisher, Simon E, Szepetowski, Pierre

المصدر: Roll , P , Vernes , S C , Bruneau , N , Cillario , J , Ponsole-Lenfant , M , Massacrier , A , Rudolf , G , Khalife , M , Hirsch , E , Fisher , S E & Szepetowski , P 2010 , ' Molecular networks implicated in speech-related disorders : FOXP2 regulates the SRPX2/uPAR complex ' , Human Molecular Genetics , vol. 19 , no. 24 , pp. 4848-60 . https://doi.org/10.1093/hmg/ddq415

مصطلحات موضوعية: Amino Acid Sequence, Base Sequence, Binding Sites, Consensus Sequence/genetics, Electrophoretic Mobility Shift Assay, Female, Forkhead Transcription Factors/chemistry, Gene Regulatory Networks, Genes, Reporter, HEK293 Cells, Humans, Luciferases/metabolism, Male, Malformations of Cortical Development/complications, Molecular Sequence Data, Mutation, Missense/genetics, Nerve Tissue Proteins/genetics, Pedigree, Promoter Regions, Genetic/genetics, Protein Binding, RNA, Messenger/genetics, Receptors, Urokinase Plasminogen Activator/genetics, Speech Disorders/complications

Relation: https://research-portal.st-andrews.ac.uk/en/researchoutput/molecular-networks-implicated-in-speechrelated-disorders(c6dba9e1-9abe-480b-b80d-e515a6c69e71).html

الاتاحة: https://research-portal.st-andrews.ac.uk/en/researchoutput/molecular-networks-implicated-in-speechrelated-disorders(c6dba9e1-9abe-480b-b80d-e515a6c69e71).html
https://doi.org/10.1093/hmg/ddq415

المؤلفون: Vernes, Sonja C, Nicod, Jérôme, Elahi, Fanny M, Coventry, Julie A, Kenny, Niamh, Coupe, Anne-Marie, Bird, Louise E, Davies, Kay E, Fisher, Simon E

المصدر: Vernes , S C , Nicod , J , Elahi , F M , Coventry , J A , Kenny , N , Coupe , A-M , Bird , L E , Davies , K E & Fisher , S E 2006 , ' Functional genetic analysis of mutations implicated in a human speech and language disorder ' , Human Molecular Genetics , vol. 15 , no. 21 , pp. 3154-67 . https://doi.org/10.1093/hmg/ddl392

مصطلحات موضوعية: Alternative Splicing, Amino Acid Sequence, Apraxias/genetics, Brain/metabolism, Cell Line, Cell Nucleus/metabolism, Codon, Nonsense, DNA-Binding Proteins/genetics, Forkhead Transcription Factors/chemistry, Humans, Language Development Disorders/genetics, Molecular Sequence Data, Mutagenesis, Site-Directed, Mutation, Missense, Point Mutation, Protein Isoforms/chemistry, Protein Structure, Tertiary, Recombinant Proteins/analysis, Transcriptional Activation, Transfection

الاتاحة: https://risweb.st-andrews.ac.uk/portal/en/researchoutput/functional-genetic-analysis-of-mutations-implicated-in-a-human-speech-and-language-disorder(13c3a660-3ab1-4692-9287-7fbc80ccff1f).html
https://doi.org/10.1093/hmg/ddl392

المؤلفون: Vernes, Sonja C, Nicod, Jérôme, Elahi, Fanny M, Coventry, Julie A, Kenny, Niamh, Coupe, Anne-Marie, Bird, Louise E, Davies, Kay E, Fisher, Simon E

المصدر: Vernes , S C , Nicod , J , Elahi , F M , Coventry , J A , Kenny , N , Coupe , A-M , Bird , L E , Davies , K E & Fisher , S E 2006 , ' Functional genetic analysis of mutations implicated in a human speech and language disorder ' , Human Molecular Genetics , vol. 15 , no. 21 , pp. 3154-67 . https://doi.org/10.1093/hmg/ddl392

مصطلحات موضوعية: Alternative Splicing, Amino Acid Sequence, Apraxias/genetics, Brain/metabolism, Cell Line, Cell Nucleus/metabolism, Codon, Nonsense, DNA-Binding Proteins/genetics, Forkhead Transcription Factors/chemistry, Humans, Language Development Disorders/genetics, Molecular Sequence Data, Mutagenesis, Site-Directed, Mutation, Missense, Point Mutation, Protein Isoforms/chemistry, Protein Structure, Tertiary, Recombinant Proteins/analysis, Transcriptional Activation, Transfection

الاتاحة: https://research-portal.st-andrews.ac.uk/en/publications/13c3a660-3ab1-4692-9287-7fbc80ccff1f
https://doi.org/10.1093/hmg/ddl392

المؤلفون: Vernes, Sonja C, Nicod, Jérôme, Elahi, Fanny M, Coventry, Julie A, Kenny, Niamh, Coupe, Anne-Marie, Bird, Louise E, Davies, Kay E, Fisher, Simon E

المصدر: Vernes , S C , Nicod , J , Elahi , F M , Coventry , J A , Kenny , N , Coupe , A-M , Bird , L E , Davies , K E & Fisher , S E 2006 , ' Functional genetic analysis of mutations implicated in a human speech and language disorder ' , Human Molecular Genetics , vol. 15 , no. 21 , pp. 3154-67 . https://doi.org/10.1093/hmg/ddl392

مصطلحات موضوعية: Alternative Splicing, Amino Acid Sequence, Apraxias/genetics, Brain/metabolism, Cell Line, Cell Nucleus/metabolism, Codon, Nonsense, DNA-Binding Proteins/genetics, Forkhead Transcription Factors/chemistry, Humans, Language Development Disorders/genetics, Molecular Sequence Data, Mutagenesis, Site-Directed, Mutation, Missense, Point Mutation, Protein Isoforms/chemistry, Protein Structure, Tertiary, Recombinant Proteins/analysis, Transcriptional Activation, Transfection

Relation: https://research-portal.st-andrews.ac.uk/en/researchoutput/functional-genetic-analysis-of-mutations-implicated-in-a-human-speech-and-language-disorder(13c3a660-3ab1-4692-9287-7fbc80ccff1f).html

الاتاحة: https://research-portal.st-andrews.ac.uk/en/researchoutput/functional-genetic-analysis-of-mutations-implicated-in-a-human-speech-and-language-disorder(13c3a660-3ab1-4692-9287-7fbc80ccff1f).html
https://doi.org/10.1093/hmg/ddl392

المؤلفون: Francis, RE, Madureira, PA, Varshochi, R, Constantinidou, D, Coombes, RC, Yao, KM, Lam, EWF

مصطلحات موضوعية: Transcription, Genetic, Up-Regulation, Gene Expression Regulation, Neoplastic, Humans, Forkhead Transcription Factors - Chemistry - Physiology, Biotinylation, Breast Neoplasms - Metabolism, Estrogen Receptor Alpha - Biosynthesis - Genetics, Cell Line, Tumor, Cell Cycle, Models, Oligonucleotides - Chemistry, Rna, Messenger - Metabolism

Relation: Journal of Biological Chemistry; http://www.scopus.com/mlt/select.url?eid=2-s2.0-33748755657&selection=ref&src=s&origin=recordpage; Journal Of Biological Chemistry, 2006, v. 281 n. 35, p. 25167-25176; 25176; 129003; WOS:000240031300017; 35; eid_2-s2.0-33748755657; 25167; http://hdl.handle.net/10722/147547; 281

الاتاحة: https://doi.org/10.1074/jbc.M603906200
http://hdl.handle.net/10722/147547