Geni TBX e patologia umana / / Daniela Romagno.
TBX genes belong to a family of homeotic genes (t-boxes) for which it has been proved that gene mutations have serious consequences on the development. In particular, there is significant evidence to support the involvement of the TBX1 gene in DiGeorge / Velocardiofacial syndrome (DGS/VCFS) and it h...
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| Superior document: | Scuole di dottorato |
|---|---|
| : | |
| Year of Publication: | 2002 |
| Language: | Italian |
| Series: | Tesi: Scienze / Università degli studi di Firenze ;
1 |
| Physical Description: | 1 online resource (78 p.) |
| Notes: | Thesis. |
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| 100 | 1 | |a Romagno, Daniela. | |
| 245 | 1 | 0 | |a Geni TBX e patologia umana / |c Daniela Romagno. |h [electronic resource] |
| 260 | |a Firenze : |b Firenze university press, |c 2002. | ||
| 300 | |a 1 online resource (78 p.) | ||
| 336 | |a text |b txt | ||
| 337 | |a computer |b c | ||
| 338 | |a online resource |b cr | ||
| 440 | 0 | |a Tesi: Scienze / Università degli studi di Firenze ; |v 1 | |
| 490 | 1 | |a Scuole di dottorato | |
| 500 | |a Thesis. | ||
| 504 | |a Includes bibliographical references. | ||
| 546 | |a Italian | ||
| 520 | |a TBX genes belong to a family of homeotic genes (t-boxes) for which it has been proved that gene mutations have serious consequences on the development. In particular, there is significant evidence to support the involvement of the TBX1 gene in DiGeorge / Velocardiofacial syndrome (DGS/VCFS) and it has been proved that the TBX3 and TBX5 genes are implicated, respectively, in UMS (Ulnar Mammary Syndhrome) and in Holt-Oram syndrome (HOS). The book collects information available in the literature up to October 2001 on human TBX genes. The review of the data allowed to come to interesting considerations and offers ideas for orienting further research. | ||
| 650 | 0 | |a Genetics. | |
| 650 | 0 | |a Pathology. | |
| 650 | 2 | |a Congenital, Hereditary, and Neonatal Diseases and Abnormalities | |
| 650 | 2 | |a Genetic Processes | |
| 650 | 2 | |a DNA-Binding Proteins | |
| 650 | 2 | |a Transcription Factors | |
| 650 | 2 | |a Genetic Phenomena | |
| 650 | 2 | |a Proteins | |
| 650 | 2 | |a Diseases | |
| 650 | 2 | |a Amino Acids, Peptides, and Proteins | |
| 650 | 2 | |a Drug Therapy | |
| 650 | 2 | |a Mutagenesis | |
| 650 | 2 | |a T-Box Domain Proteins | |
| 650 | 2 | |a Congenital Abnormalities | |
| 653 | |a Medicina | ||
| 653 | |a Genetica | ||
| 653 | |a DNA | ||
| 653 | |a Open Access | ||
| 906 | |a BOOK | ||
| 999 | |a This Record contains information from the Harvard Library Bibliographic Dataset, which is provided by the Harvard Library under its Bibliographic Dataset Use Terms and includes data made available by, among others the Library of Congress | ||
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