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...

Full description

Saved in:
Bibliographic Details
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.
Tags: Add Tag
No Tags, Be the first to tag this record!
id 993546856704498
ctrlnum (CKB)1000000000280060
(ItFiC)it02717077
(MH)011326184-5
(SSID)ssj0000576840
(PQKBManifestationID)12187087
(PQKBTitleCode)TC0000576840
(PQKBWorkID)10558943
(PQKB)10471506
(oapen)https://directory.doabooks.org/handle/20.500.12854/83697
(EXLCZ)991000000000280060
collection bib_alma
record_format marc
spelling Romagno, Daniela.
Geni TBX e patologia umana / Daniela Romagno. [electronic resource]
Firenze : Firenze university press, 2002.
1 online resource (78 p.)
text txt
computer c
online resource cr
Tesi: Scienze / Università degli studi di Firenze ; 1
Scuole di dottorato
Thesis.
Includes bibliographical references.
Italian
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.
Genetics.
Pathology.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Processes
DNA-Binding Proteins
Transcription Factors
Genetic Phenomena
Proteins
Diseases
Amino Acids, Peptides, and Proteins
Drug Therapy
Mutagenesis
T-Box Domain Proteins
Congenital Abnormalities
Medicina
Genetica
DNA
Open Access
language Italian
format Electronic
eBook
author Romagno, Daniela.
spellingShingle Romagno, Daniela.
Geni TBX e patologia umana /
Scuole di dottorato
author_facet Romagno, Daniela.
author_variant d r dr
author_sort Romagno, Daniela.
title Geni TBX e patologia umana /
title_full Geni TBX e patologia umana / Daniela Romagno. [electronic resource]
title_fullStr Geni TBX e patologia umana / Daniela Romagno. [electronic resource]
title_full_unstemmed Geni TBX e patologia umana / Daniela Romagno. [electronic resource]
title_auth Geni TBX e patologia umana /
title_new Geni TBX e patologia umana /
title_sort geni tbx e patologia umana /
series Scuole di dottorato
series2 Scuole di dottorato
publisher Firenze university press,
publishDate 2002
physical 1 online resource (78 p.)
isbn 88-8453-055-5
callnumber-first Q - Science
callnumber-subject QH - Natural History and Biology
callnumber-label QH431
callnumber-sort QH 3431
illustrated Not Illustrated
dewey-hundreds 500 - Science
dewey-tens 570 - Life sciences; biology
dewey-ones 575 - Specific parts of & systems in plants
dewey-full 575
dewey-sort 3575
dewey-raw 575
dewey-search 575
work_keys_str_mv AT romagnodaniela genitbxepatologiaumana
status_str n
ids_txt_mv (CKB)1000000000280060
(ItFiC)it02717077
(MH)011326184-5
(SSID)ssj0000576840
(PQKBManifestationID)12187087
(PQKBTitleCode)TC0000576840
(PQKBWorkID)10558943
(PQKB)10471506
(oapen)https://directory.doabooks.org/handle/20.500.12854/83697
(EXLCZ)991000000000280060
carrierType_str_mv cr
hierarchy_parent_title Scuole di dottorato
is_hierarchy_title Geni TBX e patologia umana /
container_title Scuole di dottorato
_version_ 1796649042823872513
fullrecord <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01899nam a22005652i 4500</leader><controlfield tag="001">993546856704498</controlfield><controlfield tag="005">20220812175939.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr|mn|---annan</controlfield><controlfield tag="008">050504s2002 it o 000 0 ita d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">88-8453-055-5</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(CKB)1000000000280060</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ItFiC)it02717077</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(MH)011326184-5</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SSID)ssj0000576840</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(PQKBManifestationID)12187087</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(PQKBTitleCode)TC0000576840</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(PQKBWorkID)10558943</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(PQKB)10471506</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(oapen)https://directory.doabooks.org/handle/20.500.12854/83697</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLCZ)991000000000280060</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">ItFiC</subfield><subfield code="b">eng</subfield><subfield code="c">ItFiC</subfield><subfield code="d">MH</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">ita</subfield></datafield><datafield tag="045" ind1=" " ind2=" "><subfield code="a">x4x-</subfield></datafield><datafield tag="050" ind1=" " ind2="4"><subfield code="a">QH431</subfield></datafield><datafield tag="082" ind1="1" ind2="4"><subfield code="a">575</subfield><subfield code="2">21</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Romagno, Daniela.</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Geni TBX e patologia umana /</subfield><subfield code="c">Daniela Romagno.</subfield><subfield code="h">[electronic resource]</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Firenze :</subfield><subfield code="b">Firenze university press,</subfield><subfield code="c">2002.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (78 p.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield></datafield><datafield tag="440" ind1=" " ind2="0"><subfield code="a">Tesi: Scienze / Università degli studi di Firenze ;</subfield><subfield code="v">1</subfield></datafield><datafield tag="490" ind1="1" ind2=" "><subfield code="a">Scuole di dottorato</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Thesis.</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">Italian</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="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.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genetics.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Pathology.</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Congenital, Hereditary, and Neonatal Diseases and Abnormalities</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Genetic Processes</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">DNA-Binding Proteins</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Transcription Factors</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Genetic Phenomena</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Proteins</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Diseases</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Amino Acids, Peptides, and Proteins</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Drug Therapy</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Mutagenesis</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">T-Box Domain Proteins</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Congenital Abnormalities</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Medicina</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Genetica</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">DNA</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Open Access</subfield></datafield><datafield tag="906" ind1=" " ind2=" "><subfield code="a">BOOK</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="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</subfield></datafield><datafield tag="ADM" ind1=" " ind2=" "><subfield code="b">2023-02-22 20:24:37 Europe/Vienna</subfield><subfield code="f">system</subfield><subfield code="c">marc21</subfield><subfield code="a">2012-02-26 00:26:26 Europe/Vienna</subfield><subfield code="g">false</subfield></datafield><datafield tag="AVE" ind1=" " ind2=" "><subfield code="i">DOAB Directory of Open Access Books</subfield><subfield code="P">DOAB Directory of Open Access Books</subfield><subfield code="x">https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&amp;portfolio_pid=5338349560004498&amp;Force_direct=true</subfield><subfield code="Z">5338349560004498</subfield><subfield code="b">Available</subfield><subfield code="8">5338349560004498</subfield></datafield></record></collection>