Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 95

1.

The frequency of granulocytes with spontaneous somatic mutations: a wide distribution in a normal human population.

Rondelli T, Berardi M, Peruzzi B, Boni L, Caporale R, Dolara P, Notaro R, Luzzatto L.

PLoS One. 2013;8(1):e54046. doi: 10.1371/journal.pone.0054046. Epub 2013 Jan 14.

PMID:
23342069
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

The use of PIG-A as a sentinel gene for the study of the somatic mutation rate and of mutagenic agents in vivo.

Peruzzi B, Araten DJ, Notaro R, Luzzatto L.

Mutat Res. 2010 Jul-Sep;705(1):3-10. doi: 10.1016/j.mrrev.2009.12.004. Epub 2009 Dec 24. Review.

PMID:
20034593
[PubMed - indexed for MEDLINE]
3.

The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuria.

Ware RE, Nishimura J, Moody MA, Smith C, Rosse WF, Howard TA.

Blood. 1998 Oct 1;92(7):2541-50.

PMID:
9746796
[PubMed - indexed for MEDLINE]
Free Article
4.

Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria.

Purow DB, Howard TA, Marcus SJ, Rosse WF, Ware RE.

Blood Cells Mol Dis. 1999 Apr;25(2):81-91.

PMID:
10389589
[PubMed - indexed for MEDLINE]
5.

Monitoring humans for somatic mutation in the endogenous PIG-a gene using red blood cells.

Dobrovolsky VN, Elespuru RK, Bigger CA, Robison TW, Heflich RH.

Environ Mol Mutagen. 2011 Dec;52(9):784-94. doi: 10.1002/em.20667. Epub 2011 Aug 8.

PMID:
21826740
[PubMed - indexed for MEDLINE]
6.

A quantitative measurement of the human somatic mutation rate.

Araten DJ, Golde DW, Zhang RH, Thaler HT, Gargiulo L, Notaro R, Luzzatto L.

Cancer Res. 2005 Sep 15;65(18):8111-7. Erratum in: Cancer Res. 2005 Nov 15;65(22):10635.

PMID:
16166284
[PubMed - indexed for MEDLINE]
Free Article
7.

A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones.

Nishimura J, Inoue N, Wada H, Ueda E, Pramoonjago P, Hirota T, Machii T, Kageyama T, Kanamaru A, Takeda J, Kinoshita T, Kitani T.

Blood. 1997 May 1;89(9):3470-6.

PMID:
9129055
[PubMed - indexed for MEDLINE]
Free Article
8.

Genotypic and phenotypic implications in paroxysmal nocturnal hemoglobinuria (PNH): a preliminary investigation.

Pakdeesuwan K, Siripanyaphinyo U, Pramoonjago P, Pattanapanyasat K, Wilairat P, Kinoshita T, Wanachiwanawin W.

Southeast Asian J Trop Med Public Health. 1997;28 Suppl 3:58-63.

PMID:
9640601
[PubMed - indexed for MEDLINE]
9.

The distribution of PIG-A gene abnormalities in paroxysmal nocturnal hemoglobinuria granulocytes and cultured erythroblasts.

Noji H, Shichishima T, Saitoh Y, Kai T, Yamamoto T, Ogawa K, Okamoto M, Ikeda K, Maruyama Y.

Exp Hematol. 2001 Apr;29(4):391-400.

PMID:
11301179
[PubMed - indexed for MEDLINE]
10.

JAK2 (V617F) as an acquired somatic mutation and a secondary genetic event associated with disease progression in familial myeloproliferative disorders.

Rumi E, Passamonti F, Pietra D, Della Porta MG, Arcaini L, Boggi S, Elena C, Boveri E, Pascutto C, Lazzarino M, Cazzola M.

Cancer. 2006 Nov 1;107(9):2206-11.

PMID:
16998940
[PubMed - indexed for MEDLINE]
Free Article
11.

Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene.

Bessler M, Mason PJ, Hillmen P, Miyata T, Yamada N, Takeda J, Luzzatto L, Kinoshita T.

EMBO J. 1994 Jan 1;13(1):110-7.

PMID:
8306954
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

The mutation rate in PIG-A is normal in patients with paroxysmal nocturnal hemoglobinuria (PNH).

Araten DJ, Luzzatto L.

Blood. 2006 Jul 15;108(2):734-6. Epub 2006 Mar 16.

PMID:
16543465
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria.

Miyata T, Yamada N, Iida Y, Nishimura J, Takeda J, Kitani T, Kinoshita T.

N Engl J Med. 1994 Jan 27;330(4):249-55.

PMID:
8272086
[PubMed - indexed for MEDLINE]
Free Article
14.

Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals.

Araten DJ, Nafa K, Pakdeesuwan K, Luzzatto L.

Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5209-14.

PMID:
10220445
[PubMed - indexed for MEDLINE]
Free PMC Article
15.
16.

PIG-A gene abnormalities in Thai patients with paroxysmal nocturnal hemoglobinuria.

Pramoonjago P, Wanachiwanawin W, Chinprasertsuk S, Pattanapanyasat K, Takeda J, Kinoshita T.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:322-4.

PMID:
8629134
[PubMed - indexed for MEDLINE]
17.

Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes.

Ware RE, Pickens CV, DeCastro CM, Howard TA.

Exp Hematol. 2001 Dec;29(12):1403-9.

PMID:
11750098
[PubMed - indexed for MEDLINE]
18.

Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: a novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma.

Centeno I, Blay P, Santamaría I, Astudillo A, Pitiot AS, Osorio FG, González-Arriaga P, Iglesias F, Menéndez P, Tardón A, Freije JM, Balbín M.

BMC Cancer. 2011 May 16;11:172. doi: 10.1186/1471-2407-11-172.

PMID:
21575252
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Human in vivo somatic mutation measured at two loci: individuals with stably elevated background erythrocyte glycophorin A (gpa) variant frequencies exhibit normal T-lymphocyte hprt mutant frequencies.

Bigbee WL, Fuscoe JC, Grant SG, Jones IM, Gorvad AE, Harrington-Brock K, Strout CL, Thomas CB, Moore MM.

Mutat Res. 1998 Feb 2;397(2):119-36.

PMID:
9541637
[PubMed - indexed for MEDLINE]
20.

CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia.

Azenishi Y, Ueda E, Machii T, Nishimura J, Hirota T, Shibano M, Nakao S, Kinoshita T, Mizoguchi H, Kitani T.

Br J Haematol. 1999 Mar;104(3):523-9.

PMID:
10086790
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk