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Select item 33288161.

MENX and MEN4

Natalia S. Pellegata

Clinics (Sao Paulo) 2012 Apr; 67(Suppl 1): 13–18. doi: 10.6061/clinics/2012(Sup01)04

PMCID:: PMC3328816

Abstract Article PDF–1.6M

Select item 36053972.

A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype

Gianluca Occhi, Daniela Regazzo, Giampaolo Trivellin, Francesca Boaretto, Denis Ciato, Sara Bobisse, Sergio Ferasin, Filomena Cetani, Elena Pardi, Márta Korbonits, Natalia S. Pellegata, Viktoryia Sidarovich, Alessandro Quattrone, Giuseppe Opocher, Franco Mantero, Carla Scaroni

PLoS Genet. 2013 Mar; 9(3): e1003350. Published online 2013 Mar 21. doi: 10.1371/journal.pgen.1003350

PMCID:: PMC3605397

Abstract Article PDF–1.2M

Select item 40825313.

Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)

Rajesh V. Thakker

Mol Cell Endocrinol. 2014 Apr 5; 386(1-2): 2–15. doi: 10.1016/j.mce.2013.08.002

PMCID:: PMC4082531

Abstract Article

Select item 44979464.

MEN1, MEN4, and Carney Complex: Pathology and Molecular Genetics

Marie Helene Schernthaner-Reiter, Giampaolo Trivellin, Constantine A. Stratakis

Neuroendocrinology. Author manuscript; available in PMC 2017 Jan 1.

Published in final edited form as: Neuroendocrinology. 2016; 103(1): 18–31. Published online 2015 Jan 9. doi: 10.1159/000371819

PMCID:: PMC4497946

Abstract Article PDF–371K

Select item 98749645.

Multiple endocrine neoplasia type 4: a new member of the MEN family

Hélène Singeisen, Mariko Melanie Renzulli, Vojtech Pavlicek, Pascal Probst, Fabian Hauswirth, Markus K Muller, Magdalene Adamczyk, Achim Weber, Reto Martin Kaderli, Pietro Renzulli

Endocr Connect. 2023 Feb 1; 12(2): e220411. Published online 2023 Jan 24. doi: 10.1530/EC-22-0411

PMCID:: PMC9874964

Abstract Article PDF–928K

Select item 92823586.

MEN4, the MEN1 Mimicker: A Case Series of three Phenotypically Heterogenous Patients With Unique CDKN1B Mutations

Amanda Seabrook, Ayanthi Wijewardene, Sunita De Sousa, Tang Wong, Nisa Sheriff, Anthony J Gill, Rakesh Iyer, Michael Field, Catherine Luxford, Roderick Clifton-Bligh, Ann McCormack, Katherine Tucker

J Clin Endocrinol Metab. 2022 Aug; 107(8): 2339–2349. Published online 2022 Mar 22. doi: 10.1210/clinem/dgac162

PMCID:: PMC9282358

Abstract Article

Select item 89596487.

Case Report: New CDKN1B Mutation in Multiple Endocrine Neoplasia Type 4 and Brief Literature Review on Clinical Management

Elisabetta Lavezzi, Alessandro Brunetti, Valeria Smiroldo, Gennaro Nappo, Vittorio Pedicini, Eleonora Vitali, Giampaolo Trivellin, Gherardo Mazziotti, Andrea Lania

Front Endocrinol (Lausanne) 2022; 13: 773143. Published online 2022 Mar 9. doi: 10.3389/fendo.2022.773143

PMCID:: PMC8959648

Abstract Article PDF–360K

Select item 56239378.

MEN4 and CDKN1B mutations: The latest of the MEN syndromes

Rami Alrezk, Fady Hannah-Shmouni, Constantine A. Stratakis

Endocr Relat Cancer. Author manuscript; available in PMC 2018 Oct 1.

Published in final edited form as: Endocr Relat Cancer. 2017 Oct; 24(10): T195–T208. Published online 2017 Aug 19. doi: 10.1530/ERC-17-0243

PMCID:: PMC5623937

Abstract Article PDF–594K

Select item 57131519.

Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4

Elena Pardi, Stefano Mariotti, Natalia S Pellegata, Katiuscia Benfini, Simona Borsari, Federica Saponaro, Liborio Torregrossa, Antonello Cappai, Chiara Satta, Marco Mastinu, Claudio Marcocci, Filomena Cetani

Endocr Connect. 2015 Mar 1; 4(1): 1–8. Published online 2014 Dec 17. doi: 10.1530/EC-14-0116

PMCID:: PMC5713151

Abstract Article PDF–319K

Select item 663778810.

Clinical Features of Multiple Endocrine Neoplasia Type 4: Novel Pathogenic Variant and Review of Published Cases

Anja Frederiksen, Maria Rossing, Pernille Hermann, Charlotte Ejersted, Rajesh V Thakker, Morten Frost

J Clin Endocrinol Metab. 2019 Sep; 104(9): 3637–3646. Published online 2019 Apr 16. doi: 10.1210/jc.2019-00082

PMCID:: PMC6637788

Abstract Article

Select item 719003111.

Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing’s Disease With or Without an MEN4 Phenotype

Fanny Chasseloup, Nathan Pankratz, John Lane, Fabio R Faucz, Margaret F Keil, Prashant Chittiboina, Denise M Kay, Tara Hussein Tayeb, Constantine A Stratakis, James L Mills, Laura C Hernández-Ramírez

J Clin Endocrinol Metab. 2020 Jun; 105(6): 1983–2005. Published online 2020 Mar 31. doi: 10.1210/clinem/dgaa160

PMCID:: PMC7190031

Abstract Article

Select item 1110617412.

Syndromic MEN1 parathyroid adenomas consist of both subclonal nodules and clonally independent tumors

Konstantin Bräutigam, Cédric Nesti, Philipp Riss, Christian Scheuba, Bruno Niederle, Tobias Grob, Annunziata Di Domenico, Maja Neuenschwander, Peter Mazal, Nastassja Köhn, Roman Trepp, Aurel Perren, Reto M. Kaderli

Virchows Arch. 2024; 484(5): 789–798. Published online 2024 Jan 20. doi: 10.1007/s00428-023-03730-3

PMCID:: PMC11106174

Abstract Article PDF–1.1M

Select item 269200713.

MUM ENHANCERS are important for seed coat mucilage production and mucilage secretory cell differentiation in Arabidopsis thaliana

Andrej A. Arsovski, Maria M. Villota, Owen Rowland, Rajagopal Subramaniam, Tamara L. Western

J Exp Bot. 2009 Jul; 60(9): 2601–2612. Published online 2009 Apr 28. doi: 10.1093/jxb/erp102

PMCID:: PMC2692007

Abstract Article PDF–987K

Select item 471642914.

Uncommon association of cerebral meningioma, parathyroid adenoma and papillary thyroid carcinoma in a patient harbouring a rare germline variant in the CDKN1B gene

Maria João Bugalho, Rita Domingues

BMJ Case Rep. 2016; 2016: bcr2015213934. Published online 2016 Jan 13. doi: 10.1136/bcr-2015-213934

PMCID:: PMC4716429

Abstract Article PDF–226K

Select item 543984115.

Familial Isolated Pituitary Adenomas: From Genetics to Therapy

Federica Guaraldi, Roberto Salvatori

Clin Transl Sci. 2011 Feb; 4(1): 55–62. Published online 2011 Feb 23. doi: 10.1111/j.1752-8062.2010.00254.x

PMCID:: PMC5439841

Abstract Article PDF–631K

Select item 554788916.

Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: clinical features, genetics and surveillance recommendations in childhood

Jonathan D. Wasserman, Gail E. Tomlinson, Harriet Druker, Junne Kamihara, Wendy K. Kohlmann, Christian P. Kratz, Katherine L. Nathanson, Kristian W. Pajtler, Andreu Parareda, Surya P. Rednam, Lisa J. States, Anita Villani, Michael F. Walsh, Kristin Zelley, Joshua D. Schiffman

Clin Cancer Res. Author manuscript; available in PMC 2018 Jul 1.

Published in final edited form as: Clin Cancer Res. 2017 Jul 1; 23(13): e123–e132. doi: 10.1158/1078-0432.CCR-17-0548

PMCID:: PMC5547889

Abstract Article PDF–753K

Select item 1009269117.

Epidemiology, Pathophysiology, and Genetics of Primary Hyperparathyroidism

Salvatore Minisola, Andrew Arnold, Zhanna Belaya, Maria Luisa Brandi, Bart L. Clarke, Fadil M. Hannan, Lorenz C. Hofbauer, Karl L. Insogna, André Lacroix, Uri Liberman, Andrea Palermo, Jessica Pepe, René Rizzoli, Robert Wermers, Rajesh V. Thakker

J Bone Miner Res. 2022 Nov; 37(11): 2315–2329. Published online 2022 Oct 17. doi: 10.1002/jbmr.4665

PMCID:: PMC10092691

Abstract Article PDF–606K

Select item 1053123718.

Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors

Antongiulio Faggiano, Beatrice Fazzalari, Nevena Mikovic, Flaminia Russo, Virginia Zamponi, Rossella Mazzilli, Vito Guarnieri, Maria Piane, Vincenzo Visco, Simona Petrucci

Genes (Basel) 2023 Sep; 14(9): 1782. Published online 2023 Sep 10. doi: 10.3390/genes14091782

PMCID:: PMC10531237

Abstract Article PDF–255K

Select item 1055820719.

Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort

Isabel Mazarico-Altisent, Ismael Capel, Neus Baena, Maria Rosa Bella-Cueto, Santi Barcons, Xavier Guirao, Rocío Pareja, Andreea Muntean, Valeria Arsentales, Assumpta Caixàs, Mercedes Rigla

Front Endocrinol (Lausanne) 2023; 14: 1244361. Published online 2023 Sep 21. doi: 10.3389/fendo.2023.1244361