المؤلفون: Desire Collen, Maartin Haardt, Frederik De Smet, Sandra Jansen, Ann Swillen, Deborah A Driscol, Thurid Boetel, Mieke Dewerchin, Christa Maes, Peter Carmeliet, Robert Vlietinck, Jian Wang, Lieve Moons, Peter Hellings, Veerle Compernolle, Maren von der Ohe, Beverly S. Emanuel, Ingeborg Stalmans, Marc Gewillig, Stéphane Plaisance, Paige L. Kneer, Adriana C. Gittenberger-de Groot, Koenraad Devriendt, Peter J. Scambler, Diether Lambrechts, Simon J. Conway, Sunit Maity, Annett Behn-Krappa, Daniel G. M. Molin, Camila V. Esguerra, Bernice E. Morrow, Geert Carmeliet

المساهمون: Fysiologie, Populatie Genetica, RS: NUTRIM School of Nutrition and Translational Research in Metabolism, RS: CARIM School for Cardiovascular Diseases

المصدر: Nature Medicine, 9(2), 173-182. Nature Publishing Group

مصطلحات موضوعية: Vascular Endothelial Growth Factor A, TBX1, medicine.medical_specialty, Endothelial Growth Factors, Thymus Gland, General Biochemistry, Genetics and Molecular Biology, Congenital Abnormalities, Mice, Dysgenesis, Internal medicine, DiGeorge syndrome, Neuropilin 1, DiGeorge Syndrome, medicine, Animals, Protein Isoforms, Zebrafish, Mice, Knockout, Lymphokines, biology, Vascular Endothelial Growth Factors, Skull, General Medicine, medicine.disease, biology.organism_classification, Neuropilin-1, Vascular endothelial growth factor A, Endocrinology, medicine.anatomical_structure, Face, embryonic structures, Immunology, Blood Vessels, Intercellular Signaling Peptides and Proteins, Chromosome Deletion, T-Box Domain Proteins, Haploinsufficiency, Pharyngeal arch

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d12d3e38031a5d09f5018368b8b9bb9Test
https://doi.org/10.1038/nm819Test

المؤلفون: Vijaya Potluri, Raju Kucherlapati, Jun Liao, Sandra Merscher-Gomez, Jonathan A. Epstein, Lazaros K. Kochilas, Bernice E. Morrow, Min Min Lu

المصدر: Developmental Biology. 251:157-166

مصطلحات موضوعية: aortic arches, TBX1, Biology, Aortic arches, pharyngeal arches, smooth muscle, Mice, 03 medical and health sciences, 0302 clinical medicine, Chromosome 16, DiGeorge syndrome, DiGeorge Syndrome, Morphogenesis, medicine, Animals, Molecular Biology, 030304 developmental biology, 0303 health sciences, Genetic disorder, Neural crest, Tbx1, Heart, Cell Biology, Anatomy, medicine.disease, Neural crest cell differentiation, Disease Models, Animal, medicine.anatomical_structure, Neural Crest, T-Box Domain Proteins, 030217 neurology & neurosurgery, Pharyngeal arch, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25cedb422003ac541ea7924aca71a3f1Test
https://doi.org/10.1006/dbio.2002.0819Test

المؤلفون: Pe'er Dar, Susan J. Gross, Birgit Funke, Jose Ferreira, Irwin R. Merkatz, Bernice E. Morrow, Dineo Khabele

المصدر: American Journal of Obstetrics and Gynecology. 187:457-462

مصطلحات موضوعية: Male, DNA, Complementary, Microarray, Placenta, Aneuploidy, Prenatal diagnosis, Biology, Pregnancy, Prenatal Diagnosis, medicine, Humans, Northern blot, Oligonucleotide Array Sequence Analysis, Expressed Sequence Tags, Expressed sequence tag, Gene Expression Profiling, Gene Expression Regulation, Developmental, Obstetrics and Gynecology, Blotting, Northern, medicine.disease, Molecular biology, Gene expression profiling, embryonic structures, RNA, Female, Down Syndrome, DNA microarray, Trisomy

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1141f66c6ac8a3eff22c2b1dec22ab4Test
https://doi.org/10.1067/mob.2002.123542Test

المؤلفون: Deyou Zheng, Raquel Castellanos, Qing Xie, Ales Cvekl, Bernice E. Morrow

المصدر: PLoS ONE
PLoS ONE, Vol 9, Iss 5, p e95151 (2014)

مصطلحات موضوعية: Transcription, Genetic, lcsh:Medicine, medicine.disease_cause, Chromosomal Disorders, Mice, Molecular Cell Biology, Morphogenesis, Medicine and Health Sciences, lcsh:Science, Genetics, Mutation, Multidisciplinary, GATA6, Tandem Repeat Sequences, Research Article, Protein Binding, DNA transcription, Mutation, Missense, Biology, Response Elements, Cell Line, Molecular Genetics, Tandem repeat, stomatognathic system, Consensus sequence, medicine, DiGeorge Syndrome, Animals, Humans, Birth Defects, Gene, Transcription factor, Clinical Genetics, Biology and life sciences, lcsh:R, Human Genetics, DNA-binding domain, Cell Biology, Mice, Mutant Strains, Gene regulation, DNA binding site, Amino Acid Substitution, Gene Expression Regulation, Genetics of Disease, lcsh:Q, Gene expression, Gene Function, T-Box Domain Proteins, Developmental Biology, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e35113487203b2b6494f7dcda208a91Test
http://europepmc.org/articles/PMC4010391Test

المؤلفون: Tingwei Guo, Courtney Carpenter, Bernice E. Morrow, Silvia E. Racedo, Deyou Zheng, Ping Kong, Tao Wang, Stephania Macchiarulo, Zunju Hu

مصطلحات موضوعية: TBX1, medicine.medical_specialty, Mesoderm, Cell Survival, Cellular differentiation, Embryonic Development, Apoptosis, Biology, Mice, Internal medicine, DiGeorge syndrome, Genetics, medicine, Mesoderm Cell, Animals, Molecular Biology, Genetics (clinical), Mice, Knockout, Muscles, Embryogenesis, Cell Differentiation, General Medicine, Articles, medicine.disease, Cell biology, Facial muscles, medicine.anatomical_structure, Endocrinology, embryonic structures, Mastication, Pharynx, T-Box Domain Proteins, Pharyngeal arch

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7be31b62569eaeae281cb04b00ff805dTest
https://europepmc.org/articles/PMC4103673Test/

المؤلفون: Daryl A. Scott, Gunnar Houge, Sau Wai Cheung, Hitisha P. Zaveri, Himanshu Goel, Katharine E. Shelly, Britt-Marie Anderlid, Tara Montgomery, Andres Hernandez-Garcia, Arie van Haeringen, Chirag J. Patel, Tyler F. Beck, Bernice E. Morrow, Seema R. Lalani

المصدر: PLoS ONE
PLoS ONE, Vol 9, Iss 1, p e85600 (2014)
PLoS ONE, 9(1)

مصطلحات موضوعية: Candidate gene, Cardiovascular Abnormalities, Cardiomyopathy, Gene Identification and Analysis, lcsh:Medicine, Biology, Bioinformatics, Cardiovascular, Pediatrics, Molecular Genetics, Chromosomal Disorders, Cytogenetics, Pediatric Cardiology, medicine, Genetics, Humans, lcsh:Science, PDPN, Clinical Genetics, Multidisciplinary, CLCNKA, lcsh:R, Congenital Heart Disease, Chromosome, Chromosomal Deletions and Duplications, Dilated cardiomyopathy, Human Genetics, medicine.disease, Phenotype, Cardiovascular Diseases, Chromosomes, Human, Pair 1, Genetics of Disease, biology.protein, Medicine, lcsh:Q, Haploinsufficiency, Cardiomyopathies, Gene Deletion, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a9f363e7d4dfc797b59297591947fbTest
http://europepmc.org/articles/PMC3893250Test

المؤلفون: Pavel Stankiewicz, Lisa G. Shaffer, Lisa Edelmann, Raj K. Pandita, James R. Lupski, Bernice E. Morrow, Elizabeth Spiteri

المصدر: Genome Research. 11:208-217

مصطلحات موضوعية: Letter, Pan troglodytes, Sequence analysis, Chromosomes, Human, Pair 22, Molecular Sequence Data, Sequence alignment, Locus (genetics), Biology, Evolution, Molecular, Mice, Genes, Duplicate, Gene Duplication, DiGeorge syndrome, Gene duplication, DiGeorge Syndrome, medicine, Genetics, Animals, Humans, Amino Acid Sequence, Gene, Genetics (clinical), Extracellular Matrix Proteins, Gorilla gorilla, Base Sequence, Chromosome Mapping, Nuclear Proteins, Proteins, Sequence Analysis, DNA, Evolutionary pressure, Low copy repeats, medicine.disease, Macaca mulatta, Cebidae, Protein Biosynthesis, Sequence Alignment, Biomarkers

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18760e1e3f5dfd94595eef33631142d6Test
https://doi.org/10.1101/gr.143101Test

المؤلفون: Laina Freyer, Sonja Nowotschin, Antonio Baldini, Bernice E. Morrow, Melinda K. Pirity

المساهمون: Freyer, L, Nowotschin, S, Pirity, Mk, Baldini, Antonio, Morrow, Be

المصدر: BMC developmental biology (Online) (2013).
info:cnr-pdr/source/autori:Freyer L, Nowotschin S, Pirity MK, Baldini A, Morrow BE./titolo:Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice/doi:/rivista:BMC developmental biology (Online)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
BMC Developmental Biology

مصطلحات موضوعية: TBX1, RNA, Untranslated, Recombinant Fusion Proteins, Green Fluorescent Proteins, Gene Dosage, Biology, Mouse model, Mice, 03 medical and health sciences, 0302 clinical medicine, stomatognathic system, DiGeorge syndrome, VCFS/DGS, medicine, Animals, Gain-of-function, Inner ear, 030304 developmental biology, Genetics, 0303 health sciences, Heart development, Methodology Article, Neurogenesis, Tbx1, Ear, Heart, Embryo, Mammalian, medicine.disease, Fusion protein, Rosa26, Cell biology, medicine.anatomical_structure, Models, Animal, embryonic structures, Otic vesicle, T-Box Domain Proteins, Transcription Factor Gene, 030217 neurology & neurosurgery, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21216652d0d1ce64a51018be3ad53de9Test
https://doi.org/10.1186/1471-213x-13-33Test

المؤلفون: N. McCain, J. Fox, D. Blumenthal, Lisa G. Shaffer, Bernice E. Morrow, Rosalie Goldberg, Elizabeth Spiteri, Raj K. Pandita, Seema R. Lalani, S. Duong, Lisa Edelmann

المصدر: The American Journal of Human Genetics. 65:1608-1616

مصطلحات موضوعية: Male, Heterozygote, Chromosomes, Human, Pair 22, DNA Mutational Analysis, Molecular Sequence Data, Population, Translocation(s), constitutional t(11, 23), Chromosome 22q11, Aneuploidy, Translocation Breakpoint, Chromosomal translocation, Hybrid Cells, Biology, Translocation, Genetic, 03 medical and health sciences, Nondisjunction, Genetic, Cricetinae, Genetics, medicine, Chromosome 11q23, Animals, Humans, Genetics(clinical), Cloning, Molecular, education, Der(22) syndrome, In Situ Hybridization, Fluorescence, Genetics (clinical), 030304 developmental biology, Sex Characteristics, 0303 health sciences, education.field_of_study, Base Sequence, Chromosomes, Human, Pair 11, 030305 genetics & heredity, Haplotype, Breakpoint, Chromosome, Chromosome Breakage, Articles, Syndrome, Physical Chromosome Mapping, medicine.disease, Haplotypes, Translocation(s), reciprocal, Chromosome(s), rearrangement of, Female, Chromosome breakage

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88ba957da3538bd1e6759cf8a4c0a2a1Test
https://doi.org/10.1086/302689Test

المؤلفون: Raj K. Pandita, Bernice E. Morrow, Lisa Edelmann

المصدر: The American Journal of Human Genetics. 64:1076-1086

مصطلحات موضوعية: Male, Chromosomes, Human, Pair 22, Microdeletion syndrome, 0302 clinical medicine, DiGeorge syndrome, Genetics(clinical), In Situ Hybridization, Fluorescence, Genetics (clinical), Recombination, Genetic, Genetics, 0303 health sciences, education.field_of_study, Chromosome Breakage, Syndrome, Low copy repeats, Physical Chromosome Mapping, Pedigree, Multigene Family, Female, Chromosome Deletion, Pseudogenes, Research Article, Genetic Markers, Velo-cardio-facial syndrome, Population, Chromosome Breakpoints, Chromosome 22q11, Biology, 03 medical and health sciences, Tandem repeat, Sequence Homology, Nucleic Acid, DiGeorge Syndrome, medicine, Humans, Abnormalities, Multiple, Genetic Predisposition to Disease, Deletion mapping, Rearrangement disorders, education, Repetitive Sequences, Nucleic Acid, 030304 developmental biology, Base Sequence, Haplotype, medicine.disease, DNA Fingerprinting, Molecular biology, High resolution mapping, Haplotypes, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0307a761130fd203b267d0827c861a7Test
https://doi.org/10.1086/302343Test