179 related articles for article (PubMed ID: 22542001)
1. MENX.
Pellegata NS
Ann Endocrinol (Paris); 2012 Apr; 73(2):65-70. PubMed ID: 22542001
[TBL] [Abstract][Full Text] [Related]
2. Multiple endocrine neoplasia syndromes associated with mutation of p27.
Lee M; Pellegata NS
J Endocrinol Invest; 2013 Oct; 36(9):781-7. PubMed ID: 23800691
[TBL] [Abstract][Full Text] [Related]
3. The MENX syndrome and p27: relationships with multiple endocrine neoplasia.
Molatore S; Pellegata NS
Prog Brain Res; 2010; 182():295-320. PubMed ID: 20541671
[TBL] [Abstract][Full Text] [Related]
4. MENX and MEN4.
Pellegata NS
Clinics (Sao Paulo); 2012; 67 Suppl 1(Suppl 1):13-8. PubMed ID: 22584700
[TBL] [Abstract][Full Text] [Related]
5. Animal models of multiple endocrine neoplasia.
Wiedemann T; Pellegata NS
Mol Cell Endocrinol; 2016 Feb; 421():49-59. PubMed ID: 26184857
[TBL] [Abstract][Full Text] [Related]
6. Multiple endocrine neoplasia type 4.
Lee M; Pellegata NS
Front Horm Res; 2013; 41():63-78. PubMed ID: 23652671
[TBL] [Abstract][Full Text] [Related]
7. MEN4 and
Alrezk R; Hannah-Shmouni F; Stratakis CA
Endocr Relat Cancer; 2017 Oct; 24(10):T195-T208. PubMed ID: 28824003
[TBL] [Abstract][Full Text] [Related]
8. p27kip1: a new multiple endocrine neoplasia gene?
Marinoni I; Pellegata NS
Neuroendocrinology; 2011; 93(1):19-28. PubMed ID: 20980721
[TBL] [Abstract][Full Text] [Related]
9. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans.
Pellegata NS; Quintanilla-Martinez L; Siggelkow H; Samson E; Bink K; Höfler H; Fend F; Graw J; Atkinson MJ
Proc Natl Acad Sci U S A; 2006 Oct; 103(42):15558-63. PubMed ID: 17030811
[TBL] [Abstract][Full Text] [Related]
10. Multiple endocrine neoplasia, the old and the new: a mini review.
Pasquali D; Di Matteo FM; Renzullo A; Accardo G; Esposito D; Barbato F; Colantuoni V; Circelli L; Conzo G
G Chir; 2012; 33(11-12):370-3. PubMed ID: 23140918
[TBL] [Abstract][Full Text] [Related]
11. A heterozygous frameshift mutation in exon 1 of CDKN1B gene in a patient affected by MEN4 syndrome.
Tonelli F; Giudici F; Giusti F; Marini F; Cianferotti L; Nesi G; Brandi ML
Eur J Endocrinol; 2014 Aug; 171(2):K7-K17. PubMed ID: 24819502
[TBL] [Abstract][Full Text] [Related]
12. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study.
Sekiya T; Bronstein MD; Benfini K; Longuini VC; Jallad RS; Machado MC; Goncalves TD; Osaki LH; Higashi L; Viana J; Kater C; Lee M; Molatore S; Francisco G; Chammas R; Naslavsky MS; Schlesinger D; Gama P; Duarte YA; Lebrão ML; Zatz M; Meirelles O; Liberman B; Fragoso MC; Toledo SP; Pellegata NS; Toledo RA
Endocr Relat Cancer; 2014 Jun; 21(3):395-404. PubMed ID: 24532476
[TBL] [Abstract][Full Text] [Related]
13. Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumors.
Molatore S; Kiermaier E; Jung CB; Lee M; Pulz E; Höfler H; Atkinson MJ; Pellegata NS
Mol Cancer; 2010 May; 9():116. PubMed ID: 20492666
[TBL] [Abstract][Full Text] [Related]
14. Genetic testing in multiple endocrine neoplasia and related syndromes.
Calender A
Forum (Genova); 1998; 8(2):146-59. PubMed ID: 9666051
[TBL] [Abstract][Full Text] [Related]
15. MEN4, the MEN1 Mimicker: A Case Series of three Phenotypically Heterogenous Patients With Unique CDKN1B Mutations.
Seabrook A; Wijewardene A; De Sousa S; Wong T; Sheriff N; Gill AJ; Iyer R; Field M; Luxford C; Clifton-Bligh R; McCormack A; Tucker K
J Clin Endocrinol Metab; 2022 Jul; 107(8):2339-2349. PubMed ID: 35323929
[TBL] [Abstract][Full Text] [Related]
16. Characterization of MENX-associated pituitary tumours.
Marinoni I; Lee M; Mountford S; Perren A; Bravi I; Jennen L; Feuchtinger A; Drouin J; Roncaroli F; Pellegata NS
Neuropathol Appl Neurobiol; 2013 Apr; 39(3):256-69. PubMed ID: 22524684
[TBL] [Abstract][Full Text] [Related]
17. Case Report: New CDKN1B Mutation in Multiple Endocrine Neoplasia Type 4 and Brief Literature Review on Clinical Management.
Lavezzi E; Brunetti A; Smiroldo V; Nappo G; Pedicini V; Vitali E; Trivellin G; Mazziotti G; Lania A
Front Endocrinol (Lausanne); 2022; 13():773143. PubMed ID: 35355569
[TBL] [Abstract][Full Text] [Related]
18. A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization.
Molatore S; Marinoni I; Lee M; Pulz E; Ambrosio MR; degli Uberti EC; Zatelli MC; Pellegata NS
Hum Mutat; 2010 Nov; 31(11):E1825-35. PubMed ID: 20824794
[TBL] [Abstract][Full Text] [Related]
19. Characterization of neuroendocrine tumors in heterozygous mutant MENX rats: a novel model of invasive medullary thyroid carcinoma.
Molatore S; Kügler A; Irmler M; Wiedemann T; Neff F; Feuchtinger A; Beckers J; Robledo M; Roncaroli F; Pellegata NS
Endocr Relat Cancer; 2018 Feb; 25(2):145-162. PubMed ID: 29142006
[TBL] [Abstract][Full Text] [Related]
20. Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4).
Thakker RV
Mol Cell Endocrinol; 2014 Apr; 386(1-2):2-15. PubMed ID: 23933118
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
