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Items: 1 to 20 of 24

1.

Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.

Pardi E, Borsari S, Saponaro F, Bogazzi F, Urbani C, Mariotti S, Pigliaru F, Satta C, Pani F, Materazzi G, Miccoli P, Grantaliano L, Marcocci C, Cetani F.

PLoS One. 2017 Oct 16;12(10):e0186485. doi: 10.1371/journal.pone.0186485. eCollection 2017.

2.

Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family.

Guarnieri V, Seaberg RM, Kelly C, Jean Davidson M, Raphael S, Shuen AY, Baorda F, Palumbo O, Scillitani A, Hendy GN, Cole DEC.

BMC Med Genet. 2017 Aug 3;18(1):83. doi: 10.1186/s12881-017-0445-0. Erratum in: BMC Med Genet. 2017 Sep 13;18(1):99.

3.

The in vitro and vivo effects of nuclear and cytosolic parafibromin expression on the aggressive phenotypes of colorectal cancer cells: a search of potential gene therapy target.

Zheng HC, Liu JJ, Li J, Wu JC, Yang L, Zhao GF, Zhao X, Jiang HM, Huang KQ, Li ZJ.

Oncotarget. 2017 Apr 4;8(14):23603-23612. doi: 10.18632/oncotarget.15377.

4.

Epigenetic Alterations in Parathyroid Cancers.

Verdelli C, Corbetta S.

Int J Mol Sci. 2017 Feb 1;18(2). pii: E310. doi: 10.3390/ijms18020310. Review.

5.

hPaf1/PD2 interacts with OCT3/4 to promote self-renewal of ovarian cancer stem cells.

Karmakar S, Seshacharyulu P, Lakshmanan I, Vaz AP, Chugh S, Sheinin YM, Mahapatra S, Batra SK, Ponnusamy MP.

Oncotarget. 2017 Feb 28;8(9):14806-14820. doi: 10.18632/oncotarget.14775.

6.

Drosophila CG2469 Encodes a Homolog of Human CTR9 and Is Essential for Development.

Chaturvedi D, Inaba M, Scoggin S, Buszczak M.

G3 (Bethesda). 2016 Dec 7;6(12):3849-3857. doi: 10.1534/g3.116.035196.

7.

A germline mutation of HRPT2/CDC73 (70 G>T) in an adolescent female with parathyroid carcinoma: first case report and a review of the literature.

Serrano-Gonzalez M, Shay S, Austin J, Maceri DR, Pitukcheewanont P.

J Pediatr Endocrinol Metab. 2016 Sep 1;29(9):1005-12. doi: 10.1515/jpem-2016-0109. Review.

8.

Somatic HRPT2 Mutation (Arg234X) of Parathyroid Carcinoma Associated with Slipped Capital Femoral Epiphysis: A First Case Report.

Niramitmahapanya S, Deerochanawong C, Sarinnapakorn V, Sunthornthepvarakul T, Pingsuthiwong S, Athipan P, Sangsuda Y.

J Med Assoc Thai. 2016 Feb;99 Suppl 2:S201-5.

PMID:
27266237
9.

Molecular genetics and epigenetics of nonfamilial (sporadic) parathyroid tumours.

Westin G.

J Intern Med. 2016 Dec;280(6):551-558. doi: 10.1111/joim.12458. Epub 2016 Apr 12. Review.

PMID:
27071708
10.

A Novel Mutation in a Patient with Hyperparathyroidism-Jaw Tumour Syndrome.

Bellido V, Larrañaga I, Guimón M, Martinez-Conde R, Eguia A, Perez de Nanclares G, Castaño L, Gaztambide S.

Endocr Pathol. 2016 Jun;27(2):142-6. doi: 10.1007/s12022-016-9427-6.

PMID:
26995009
11.

Determination of the catalytic activity of LEOPARD syndrome-associated SHP2 mutants toward parafibromin, a bona fide SHP2 substrate involved in Wnt signaling.

Noda S, Takahashi A, Hayashi T, Tanuma S, Hatakeyama M.

Biochem Biophys Res Commun. 2016 Jan 22;469(4):1133-9. doi: 10.1016/j.bbrc.2015.12.117. Epub 2015 Dec 29.

PMID:
26742426
12.

Ubiquitin-Dependent Turnover of MYC Antagonizes MYC/PAF1C Complex Accumulation to Drive Transcriptional Elongation.

Jaenicke LA, von Eyss B, Carstensen A, Wolf E, Xu W, Greifenberg AK, Geyer M, Eilers M, Popov N.

Mol Cell. 2016 Jan 7;61(1):54-67. doi: 10.1016/j.molcel.2015.11.007. Epub 2015 Dec 10.

13.

Global Reprogramming of Host SUMOylation during Influenza Virus Infection.

Domingues P, Golebiowski F, Tatham MH, Lopes AM, Taggart A, Hay RT, Hale BG.

Cell Rep. 2015 Nov 17;13(7):1467-1480. doi: 10.1016/j.celrep.2015.10.001. Epub 2015 Nov 5.

14.

Parafibromin Is a Component of IFN-γ-Triggered Signaling Pathways That Facilitates JAK1/2-Mediated Tyrosine Phosphorylation of STAT1.

Wei J, Lian H, Zhong B, Shu HB.

J Immunol. 2015 Sep 15;195(6):2870-8. doi: 10.4049/jimmunol.1501111. Epub 2015 Jul 31.

15.

Parathyroid Carcinoma: Diagnosis and Clinical Implications.

Duan K, Mete Ö.

Turk Patoloji Derg. 2015;31 Suppl 1:80-97. doi: 10.5146/tjpath.2015.01316. Review.

16.

Clinicopathological correlates of hyperparathyroidism.

Duan K, Gomez Hernandez K, Mete O.

J Clin Pathol. 2015 Oct;68(10):771-87. doi: 10.1136/jclinpath-2015-203186. Epub 2015 Jul 10. Review.

PMID:
26163537
17.

The clinicopathological significances and biological functions of parafibromin expression in head and neck squamous cell carcinomas.

Zhang Z, Yang XF, Huang KQ, Ren L, Gou WF, Shen DF, Zhao S, Sun HZ, Takano Y, Zheng HC.

Tumour Biol. 2015 Dec;36(12):9487-97. doi: 10.1007/s13277-015-3618-5. Epub 2015 Jul 1.

PMID:
26124004
18.

HRPT2- (CDC73) RELATED HEREDITARY HYPERPARATHYROIDISM: A CASE SERIES FROM WESTERN INDIA.

Khadilkar KS, Budyal SR, Kasliwal R, Lila AR, Bandgar T, Shah NS.

Endocr Pract. 2015 Sep;21(9):1010-6. doi: 10.4158/EP15648.OR. Epub 2015 Jun 29.

PMID:
26121439
19.

Early-onset, severe, and recurrent primary hyperparathyroidism associated with a novel CDC73 mutation.

Shibata Y, Yamazaki M, Takei M, Uchino S, Sakurai A, Komatsu M.

Endocr J. 2015;62(7):627-32. doi: 10.1507/endocrj.EJ15-0057. Epub 2015 May 8.

20.

Protein Degradation of RNA Polymerase II-Association Factor 1(PAF1) Is Controlled by CNOT4 and 26S Proteasome.

Sun HY, Kim N, Hwang CS, Yoo JY.

PLoS One. 2015 May 1;10(5):e0125599. doi: 10.1371/journal.pone.0125599. eCollection 2015.

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