“Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)”
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1559-0100
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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“Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)” ; day:28 ; month:6 ; year:2021 ; pages:1-6
Endocrine ; (28.6.2021), 1-6
- Urheber
-
Tuli, Gerdi
Munarin, Jessica
Mussa, Alessandro
Carli, Diana
Gastaldi, Roberto
Borgia, Paola
Vigone, Maria Cristina
Abbate, Marco
Ferrero, Giovanni Battista
De Sanctis, Luisa
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1007/s12020-021-02805-y
- URN
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urn:nbn:de:101:1-2021101022391579347283
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 MESZ
Datenpartner
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Beteiligte
- Tuli, Gerdi
- Munarin, Jessica
- Mussa, Alessandro
- Carli, Diana
- Gastaldi, Roberto
- Borgia, Paola
- Vigone, Maria Cristina
- Abbate, Marco
- Ferrero, Giovanni Battista
- De Sanctis, Luisa
- SpringerLink (Online service)
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Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome
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In renal cell carcinoma the PTEN splice variant PTEN-Δ shows similar function as the tumor suppressor PTEN itself
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