Similar articles for PMID: 15712268

Year	Number of Results
1997	2
1998	2
1999	1
2000	1
2001	3
2002	2
2004	3
2005	9
2006	6
2007	5
2008	11
2009	8
2011	1
2012	1
2014	1
2016	1
2017	2
2024	0

1

Two novel mutations of the AIRE protein affecting its homodimerization properties.

Meloni A, Fiorillo E, Corda D, Perniola R, Cao A, Rosatelli MC. Meloni A, et al. Hum Mutat. 2005 Mar;25(3):319. doi: 10.1002/humu.9309. Hum Mutat. 2005. PMID: 15712268

2

APECED-causing mutations in AIRE reveal the functional domains of the protein.

Halonen M, Kangas H, Rüppell T, Ilmarinen T, Ollila J, Kolmer M, Vihinen M, Palvimo J, Saarela J, Ulmanen I, Eskelin P. Halonen M, et al. Hum Mutat. 2004 Mar;23(3):245-57. doi: 10.1002/humu.20003. Hum Mutat. 2004. PMID: 14974083

3

Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives.

Cervato S, Mariniello B, Lazzarotto F, Morlin L, Zanchetta R, Radetti G, De Luca F, Valenzise M, Giordano R, Rizzo D, Giordano C, Betterle C. Cervato S, et al. Clin Endocrinol (Oxf). 2009 Mar;70(3):421-8. doi: 10.1111/j.1365-2265.2008.03318.x. Epub 2008 Jun 27. Clin Endocrinol (Oxf). 2009. PMID: 18616706

4

A novel heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED).

Fierabracci A, Bizzarri C, Palma A, Milillo A, Bellacchio E, Cappa M. Fierabracci A, et al. Gene. 2012 Dec 10;511(1):113-7. doi: 10.1016/j.gene.2012.09.029. Epub 2012 Sep 18. Gene. 2012. PMID: 23000069

5

Functional analysis of SAND mutations in AIRE supports dominant inheritance of the G228W mutation.

Ilmarinen T, Eskelin P, Halonen M, Rüppell T, Kilpikari R, Torres GD, Kangas H, Ulmanen I. Ilmarinen T, et al. Hum Mutat. 2005 Oct;26(4):322-31. doi: 10.1002/humu.20224. Hum Mutat. 2005. PMID: 16114041

6

Aire-deficient C57BL/6 mice mimicking the common human 13-base pair deletion mutation present with only a mild autoimmune phenotype.

Hubert FX, Kinkel SA, Crewther PE, Cannon PZ, Webster KE, Link M, Uibo R, O'Bryan MK, Meager A, Forehan SP, Smyth GK, Mittaz L, Antonarakis SE, Peterson P, Heath WR, Scott HS. Hubert FX, et al. J Immunol. 2009 Mar 15;182(6):3902-18. doi: 10.4049/jimmunol.0802124. J Immunol. 2009. PMID: 19265170

7

APECED mutations in the autoimmune regulator (AIRE) gene.

Heino M, Peterson P, Kudoh J, Shimizu N, Antonarakis SE, Scott HS, Krohn K. Heino M, et al. Hum Mutat. 2001 Sep;18(3):205-11. doi: 10.1002/humu.1176. Hum Mutat. 2001. PMID: 11524731 Review.

8

Molecular background of polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome in a Polish population: novel AIRE mutations and an estimate of disease prevalence.

Stolarski B, Pronicka E, Korniszewski L, Pollak A, Kostrzewa G, Rowińska E, Włodarski P, Skórka A, Gremida M, Krajewski P, Ploski R. Stolarski B, et al. Clin Genet. 2006 Oct;70(4):348-54. doi: 10.1111/j.1399-0004.2006.00690.x. Clin Genet. 2006. PMID: 16965330

9

An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains.

Finnish-German APECED Consortium. Finnish-German APECED Consortium. Nat Genet. 1997 Dec;17(4):399-403. doi: 10.1038/ng1297-399. Nat Genet. 1997. PMID: 9398840

10

Positional cloning of the APECED gene.

Nagamine K, Peterson P, Scott HS, Kudoh J, Minoshima S, Heino M, Krohn KJ, Lalioti MD, Mullis PE, Antonarakis SE, Kawasaki K, Asakawa S, Ito F, Shimizu N. Nagamine K, et al. Nat Genet. 1997 Dec;17(4):393-8. doi: 10.1038/ng1297-393. Nat Genet. 1997. PMID: 9398839

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

53 results

Results by year