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Sara Molatore

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Chemicals & Drugs

Disorders

Physiology

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Eleonora Turco; Ilenia Ventura; Margherita Bignami; Paolo Degan; Anna Minoprio; Sara Molatore; Guglielmina Nadia Ranzani; Maria Teresa Russo; Paola Torreri; Filomena Mazzei
Understanding the role of the Q338H MUTYH variant in oxidative damage repair.
Jessica Costa-Guda; Ilaria Marinoni; Sara Molatore; Natalia S Pellegata; Andrew Arnold
Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas.
Sara Molatore; Ilaria Marinoni; Misu Lee; Elke Pulz; Maria Rosaria Ambrosio; Ettore C degli Uberti; Maria Chiara Zatelli; Natalia S Pellegata
A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization.

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All Publications

2013: Eleonora Turco; Ilenia Ventura; Margherita Bignami; Paolo Degan; Anna Minoprio; Sara Molatore; Guglielmina Nadia Ranzani; Maria Teresa Russo; Paola Torreri; Filomena Mazzei
Understanding the role of the Q338H MUTYH variant in oxidative damage repair.
Nucleic acids research 2013;41(7):4093-103.
2011: Jessica Costa-Guda; Ilaria Marinoni; Sara Molatore; Natalia S Pellegata; Andrew Arnold
Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas.
The Journal of clinical endocrinology and metabolism 2011;96(4):E701-6.
2010: Sara Molatore; Ilaria Marinoni; Misu Lee; Elke Pulz; Maria Rosaria Ambrosio; Ettore C degli Uberti; Maria Chiara Zatelli; Natalia S Pellegata
A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization.
Human mutation 2010;31(11):E1825-35.
2010: Sara Molatore; Sandya Liyanarachchi; Martin Irmler; Aurel Perren; Massimo Mannelli; Tonino Ercolino; Felix Beuschlein; Barbara Jarzab; Jan Wloch; Jacek Ziaja; Saida Zoubaa; Frauke Neff; Johannes Beckers; Heinz Höfler; Michael J Atkinson; Natalia S Pellegata
Pheochromocytoma in rats with multiple endocrine neoplasia (MENX) shares gene expression patterns with human pheochromocytoma.
Proceedings of the National Academy of Sciences of the United States of America 2010;107(43):18493-8.
2010: Sara Molatore; Maria Teresa Russo; Vito G D'Agostino; Flavia Barone; Yoshihiro Matsumoto; Alessandra M Albertini; Anna Minoprio; Paolo Degan; Filomena Mazzei; Margherita Bignami; Guglielmina Nadia Ranzani
MUTYH mutations associated with familial adenomatous polyposis: functional characterization by a mammalian cell-based assay.
Human mutation 2010;31(2):159-66.
2010: Sara Molatore; Natalia S Pellegata
The MENX syndrome and p27: relationships with multiple endocrine neoplasia.
Progress in brain research 2010;182():295-320.
2010: Sara Molatore; Eva Kiermaier; Christian B Jung; Misu Lee; Elke Pulz; Heinz Höfler; Michael J Atkinson; Natalia S Pellegata
Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumors.
Molecular cancer 2010;9():116.
2009: Maria Teresa Russo; Gabriele De Luca; Ida Casorelli; Paolo Degan; Sara Molatore; Flavia Barone; Filomena Mazzei; Tania Pannellini; Piero Musiani; Margherita Bignami
Role of MUTYH and MSH2 in the control of oxidative DNA damage, genetic instability, and tumorigenesis.
Cancer research 2009;69(10):4372-9.
2007: Francesca Cattaneo; Sara Molatore; Markos Mihalatos; Angela Apessos; Tiziana Venesio; Silvia Bione; Pierangela Grignani; Georgios Nasioulas; Guglielmina Nadia Ranzani
Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis.
Genetics in medicine : official journal of the American College of Medical Genetics 2007;9(12):836-41.
2007: Tiziana Venesio; Antonella Balsamo; Christian Sfiligoi; Luca Fuso; Sara Molatore; Guglielmina Nadia Ranzani; Mauro Risio
Constitutional high expression of an APC mRNA isoform in a subset of attenuated familial adenomatous polyposis patients.
Journal of molecular medicine (Berlin, Germany) 2007;85(3):305-12.
2006: Francesca Cattaneo; Tiziana Venesio; Sara Molatore; Antonio Russo; Roberto Fiocca; Milo Frattini; Anna Scovassi; Laura Ottini; Lucio Bertario; Guglielmina Nadia Ranzani
Functional analysis and case-control study of -160C/A polymorphism in the E-cadherin gene promoter: association with cancer risk.
Anticancer research 2006;26(6B):4627-32.
2004: Sara Molatore; Guglielmina Nadia Ranzani
Genetics of colorectal polyps.
Techniques in coloproctology 2004;8 Suppl 2():s240-2.
2004: Tiziana Venesio; Sara Molatore; Francesca Cattaneo; Arrigo Arrigoni; Mauro Risio; Guglielmina Nadia Ranzani
High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis.
Gastroenterology 2004;126(7):1681-5.