المؤلفون: Vitelli, F.

المصدر: Human Molecular Genetics ; volume 12, issue 16, page 2041-2048 ; ISSN 1460-2083

مصطلحات موضوعية: Genetics (clinical), Genetics, Molecular Biology, General Medicine

الإتاحة: https://doi.org/10.1093/hmg/ddg216Test
http://academic.oup.com/hmg/article-pdf/12/16/2041/6947780/ddg216.pdfTest

المؤلفون: Vitelli, F., Meloni, I., Fineschi, S., Favara, F., Tiziana Storlazzi, C., Rocchi, M., Renieri, A.

المصدر: Cytogenetic and Genome Research ; volume 88, issue 3-4, page 259-263 ; ISSN 1424-8581 1424-859X

مصطلحات موضوعية: Genetics (clinical), Genetics, Molecular Biology

الإتاحة: https://doi.org/10.1159/000015533Test
https://www.karger.com/Article/Pdf/15533Test

المؤلفون: Vitelli, F., De Vitis, L.R., Tedde, A., Montali, E., Papi, L.

المصدر: Cancer Genetics and Cytogenetics ; volume 91, issue 2, page 174 ; ISSN 0165-4608

مصطلحات موضوعية: Cancer Research, Genetics, Molecular Biology

الإتاحة: https://doi.org/10.1016/s0165-4608Test(97)82652-0
https://api.elsevier.com/content/article/PII:S0165460897826520?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0165460897826520?httpAccept=text/plainTest

المؤلفون: Meloni, I., Vitelli, F., Pucci, L., Lowry, R. B., Tonlorenzi, R., Rossi, E., Ventura, M., Rizzoni, G., Kashtan, C. E., Pober, B., Renieri, A.

المصدر: Journal of Medical Genetics; May2002, Vol. 39 Issue 5, p359-365, 7p, 1 Color Photograph, 3 Diagrams

مصطلحات موضوعية: INTELLECTUAL disabilities, SYNDROMES, GENES, GENETIC mutation, MEDICAL genetics, GENETICS

المؤلفون: Francesca Vitelli, Antonio Baldini

المساهمون: Vitelli, F, Baldini, Antonio, Vitelli, F., Baldini, A.

المصدر: Trends in genetics : TIG. 19(11)

مصطلحات موضوعية: TBX1, Genetics, Vascular Endothelial Growth Factor A, Candidate gene, Fibroblast Growth Factor 8, ved/biology, ved/biology.organism_classification_rank.species, Tretinoin, Biology, medicine.disease, Genetic pathways, Phenotype, Fibroblast Growth Factors, Disease Models, Animal, DiGeorge syndrome, medicine, DiGeorge Syndrome, Animals, Humans, Pharynx, Model organism, Gene, Transcription factor

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f66a936608bd0431e8f0e38f7b707c08Test
https://pubmed.ncbi.nlm.nih.gov/14585606Test

المؤلفون: Tuong Huynh, Annalisa Mupo, Francesca Vitelli, Zhen Zhang, Antonio Baldini, Angela Sobotka

المساهمون: Vitelli, F, Zhang, Z, Huynh, T, Sobotka, A, Mupo, A, Baldini, Antonio

المصدر: Developmental Biology. 295(2):559-570

مصطلحات موضوعية: TBX1, Aortic arch, animal structures, Fibroblast Growth Factor 8, 22q11 Deletion syndrome, Cardiovascular development, Aorta, Thoracic, Pharyngeal endoderm, Biology, Cardiovascular System, Bone and Bones, Article, Fgf8, Mice, FGF8, stomatognathic system, medicine.artery, medicine, Animals, Molecular Biology, Body Patterning, Genetics, Genetic interaction, Endoderm, Gene Expression Regulation, Developmental, Tbx1, Cell Biology, Pharyngeal apparatus, Phenotype, Penetrance, Mice, Mutant Strains, Cell biology, Branchial Region, medicine.anatomical_structure, Great arteries, Mutation, embryonic structures, T-Box Domain Proteins, Pharyngeal arch, Developmental Biology

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4477564caec6b7fb31d71604e74d756fTest

المؤلفون: Elizabeth A. Lindsay, Masae Morishima, Antonio Baldini, Francesca Vitelli, Ilaria Taddei

المساهمون: Vitelli, F., Morishima, M., Taddei, I., Lindsay, E. A., Baldini, Antonio

المصدر: Human molecular genetics. 11(8)

مصطلحات موضوعية: TBX1, Candidate gene, medicine.medical_specialty, Cardiovascular Abnormalities, Branchial arch, Biology, Mice, stomatognathic system, Pharyngeal apparatus, DiGeorge syndrome, Internal medicine, Neural Pathways, Peripheral Nervous System, Genetics, medicine, DiGeorge Syndrome, Animals, Molecular Biology, Genetics (clinical), Body Patterning, Endoderm, Cranial Nerves, Neural crest, General Medicine, Arteries, medicine.disease, Cranial Nerve Diseases, Cell biology, Mice, Inbred C57BL, medicine.anatomical_structure, Endocrinology, Branchial Region, Neural Crest, embryonic structures, Mutation, Haploinsufficiency, T-Box Domain Proteins, Pharyngeal arch

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f617466f722620f698fe400413a7a398Test
https://pubmed.ncbi.nlm.nih.gov/11971873Test

المؤلفون: Antonio Baldini, Tiziano Pramparo, George Ogunrinu, Francesca Vitelli, Hong Su, Tuong Huynh, Vesna Jurecic, Masae Morishima, Helen F. Sutherland, Peter J. Scambler, Allan Bradley, Elizabeth A. Lindsay

المساهمون: Lindsay, E. A., Vitelli, F., Su, H., Morishima, M., Huynh, T., Pramparo, T., Jurecic, V., Ogunrinu, G., Sutherland, H., Scambler, P., Bradley, A., Baldini, Antonio

مصطلحات موضوعية: TBX1, Molecular Sequence Data, Aorta, Thoracic, Mice, Transgenic, Biology, Cell Line, Mice, 22q11 Deletion Syndrome, Pharyngeal apparatus, DiGeorge syndrome, medicine, DiGeorge Syndrome, Animals, Humans, Genetics, Multidisciplinary, medicine.disease, Mice, Inbred C57BL, medicine.anatomical_structure, Haplotypes, Mutagenesis, Aortic Arch Syndrome, Chromosomal region, Gene Targeting, Haploinsufficiency, T-Box Domain Proteins, Pharyngeal arch, Gene Deletion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::696f5d08107b9bd3511be4b5d3b8fef8Test
http://hdl.handle.net/11386/2292347Test

المؤلفون: Francesca Vitelli, Marco Seri, Oscar Moran, Luis J. V. Galietta, Alessandra Renieri, Barbara R. Pober, Sandro Banfi, Alessandro Bulfone, Monica Piccini

المساهمون: Piccini, M, Vitelli, F, Seri, M, Galietta, Lj, Moran, O, Bulfone, A, Banfi, Sandro, Pober, B, Renieri, A., Piccini, Monica, Vitelli, Francesca, Seri, Marco, Galietta, Luis J. V., Moran, Oscar, Bulfone, Alessandro, Pober, Barbara, Renieri, Alessandra

المصدر: ResearcherID

مصطلحات موضوعية: Heart Defects, Congenital, Male, Potassium Channels, X Chromosome, Databases, Factual, Protein family, Molecular Sequence Data, Gene Expression, Nephritis, Hereditary, Contiguous gene syndrome, Homology (biology), Clone Cell, Electrocardiography, Mice, Intellectual Disability, Sequence Homology, Nucleic Acid, Gene expression, Genetics, medicine, Animals, Humans, Membrane Protein, Gene, In Situ Hybridization, Potassium Channel, biology, Animal, cDNA library, Electric Conductivity, Chromosome Mapping, Membrane Proteins, Syndrome, KCNE4, medicine.disease, Molecular biology, Clone Cells, Open reading frame, Potassium Channels, Voltage-Gated, biology.protein, Gene Deletion, Human

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8014257c85c4d6b06d92bb4283448808Test
http://hdl.handle.net/11591/217721Test

المؤلفون: Marcello Villanova, Massimo Zollo, Mirella Bruttini, Andrea Ballabio, Monica Piccini, Francesca Vitelli, Jon J. Jonsson, Giuseppe Borsani, Barbara R. Pober, Alessandra Renieri

المساهمون: Piccini, M, Vitelli, F, Bruttini, M, Pober, B. R., Jonsson, J. J., Villanova, M, Zollo, Massimo, Borsani, G, Ballabio, Andrea, Renieri, A.

مصطلحات موضوعية: Male, Saccharomyces cerevisiae Proteins, X Chromosome, Hereditary elliptocytosis, Molecular Sequence Data, Nephritis, Hereditary, Biology, ACSL4, Contiguous gene syndrome, Gene mapping, Intellectual Disability, Coenzyme A Ligases, Genetics, medicine, Humans, Amino Acid Sequence, Alport syndrome, Child, Gene, Gene map, Base Sequence, Alternative splicing, Elliptocytosis, Hereditary, Chromosome Mapping, medicine.disease, Repressor Proteins, Child, Preschool, Multigene Family, Gene Deletion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aef4d6d0415fb0c096d9a9ccf961c801Test
http://hdl.handle.net/11379/5360Test