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Similar articles for PubMed (Select 24192702)

1.

Cellular stress pathways in pediatric bone marrow failure syndromes: many roads lead to neutropenia.

Glaubach T, Minella AC, Corey SJ.

Pediatr Res. 2014 Jan;75(1-2):189-95. doi: 10.1038/pr.2013.197. Epub 2013 Nov 5. Review.

PMID:
24192702
2.

Genetic defects in severe congenital neutropenia: emerging insights into life and death of human neutrophil granulocytes.

Klein C.

Annu Rev Immunol. 2011;29:399-413. doi: 10.1146/annurev-immunol-030409-101259. Review.

PMID:
21219176
3.

Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia.

Xia J, Bolyard AA, Rodger E, Stein S, Aprikyan AA, Dale DC, Link DC.

Br J Haematol. 2009 Nov;147(4):535-42. doi: 10.1111/j.1365-2141.2009.07888.x. Epub 2009 Sep 22.

4.

Pathogenic mechanisms and clinical implications of congenital neutropenia syndromes.

Hauck F, Klein C.

Curr Opin Allergy Clin Immunol. 2013 Dec;13(6):596-606. doi: 10.1097/ACI.0000000000000014. Review.

PMID:
24145314
5.

Genetic analysis and clinical picture of severe congenital neutropenia in Israel.

Lebel A, Yacobovich J, Krasnov T, Koren A, Levin C, Kaplinsky C, Ravel-Vilk S, Laor R, Attias D, Ben Barak A, Shtager D, Stein J, Kuperman A, Miskin H, Dgany O, Giri N, Alter BP, Tamary H.

Pediatr Blood Cancer. 2015 Jan;62(1):103-8. doi: 10.1002/pbc.25251. Epub 2014 Oct 4.

PMID:
25284454
6.

Risk of myelodysplastic syndrome and acute myeloid leukemia in congenital neutropenias.

Freedman MH, Alter BP.

Semin Hematol. 2002 Apr;39(2):128-33. Review.

PMID:
11957196
7.
8.

Different pattern of gene mutations in Iranian patients with severe congenital neutropenia (including 2 new mutations).

Alizadeh Z, Fazlollahi MR, Houshmand M, Maddah M, Chavoshzadeh Z, Hamidieh AA, Shamsian BS, Eshghi P, Bolandghamat Pour S, Sadaaie Jahromi H, Mansouri M, Movahedi M, Nayebpour M, Pourpak Z, Moin M.

Iran J Allergy Asthma Immunol. 2013 Mar;12(1):86-92. doi: 012.01/ijaai.8692.

9.

Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome.

Jun HS, Lee YM, Cheung YY, McDermott DH, Murphy PM, De Ravin SS, Mansfield BC, Chou JY.

Blood. 2010 Oct 14;116(15):2783-92. doi: 10.1182/blood-2009-12-258491. Epub 2010 May 24.

10.

Genetic heterogeneity in severe congenital neutropenia: how many aberrant pathways can kill a neutrophil?

Schäffer AA, Klein C.

Curr Opin Allergy Clin Immunol. 2007 Dec;7(6):481-94. Review.

11.

Digenic mutations in severe congenital neutropenia.

Germeshausen M, Zeidler C, Stuhrmann M, Lanciotti M, Ballmaier M, Welte K.

Haematologica. 2010 Jul;95(7):1207-10. doi: 10.3324/haematol.2009.017665. Epub 2010 Mar 10.

12.

ELANE mutations in cyclic and severe congenital neutropenia: genetics and pathophysiology.

Horwitz MS, Corey SJ, Grimes HL, Tidwell T.

Hematol Oncol Clin North Am. 2013 Feb;27(1):19-41, vii. doi: 10.1016/j.hoc.2012.10.004. Epub 2012 Nov 7. Review.

13.

Survival and differentiation defects contribute to neutropenia in glucose-6-phosphatase-β (G6PC3) deficiency in a model of mouse neutrophil granulocyte differentiation.

Gautam S, Kirschnek S, Gentle IE, Kopiniok C, Henneke P, Häcker H, Malleret L, Belaaouaj A, Häcker G.

Cell Death Differ. 2013 Aug;20(8):1068-79. doi: 10.1038/cdd.2013.39. Epub 2013 May 17.

14.

Mutations of the ELA2 gene found in patients with severe congenital neutropenia induce the unfolded protein response and cellular apoptosis.

Grenda DS, Murakami M, Ghatak J, Xia J, Boxer LA, Dale D, Dinauer MC, Link DC.

Blood. 2007 Dec 15;110(13):4179-87. Epub 2007 Aug 30.

15.

Mice expressing a neutrophil elastase mutation derived from patients with severe congenital neutropenia have normal granulopoiesis.

Grenda DS, Johnson SE, Mayer JR, McLemore ML, Benson KF, Horwitz M, Link DC.

Blood. 2002 Nov 1;100(9):3221-8.

16.

Chronic idiopathic neutropenias and severe congenital neutropenia.

Palmblad J, Papadaki HA.

Curr Opin Hematol. 2008 Jan;15(1):8-14. Review.

PMID:
18043240
17.

Wnt3a stimulates maturation of impaired neutrophils developed from severe congenital neutropenia patient-derived pluripotent stem cells.

Hiramoto T, Ebihara Y, Mizoguchi Y, Nakamura K, Yamaguchi K, Ueno K, Nariai N, Mochizuki S, Yamamoto S, Nagasaki M, Furukawa Y, Tani K, Nakauchi H, Kobayashi M, Tsuji K.

Proc Natl Acad Sci U S A. 2013 Feb 19;110(8):3023-8. doi: 10.1073/pnas.1217039110. Epub 2013 Feb 4.

18.

Mesenchymal stem cells in immune-mediated bone marrow failure syndromes.

Kastrinaki MC, Pavlaki K, Batsali AK, Kouvidi E, Mavroudi I, Pontikoglou C, Papadaki HA.

Clin Dev Immunol. 2013;2013:265608. doi: 10.1155/2013/265608. Epub 2013 Dec 10. Review.

19.

Recent insights into inherited bone marrow failure syndromes.

Parikh S, Bessler M.

Curr Opin Pediatr. 2012 Feb;24(1):23-32. doi: 10.1097/MOP.0b013e32834eca77. Review.

20.

Severe congenital neutropenia and the unfolded protein response.

Xia J, Link DC.

Curr Opin Hematol. 2008 Jan;15(1):1-7. Review.

PMID:
18043239
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