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Items: 1 to 20 of 100

1.

Localization of the human GM-CSF receptor beta chain gene (CSF2RB) to chromosome 22q12.2-->q13.1.

Shen Y, Baker E, Callen DF, Sutherland GR, Willson TA, Rakar S, Gough NM.

Cytogenet Cell Genet. 1992;61(3):175-7.

PMID:
1424804
4.

Role of granulocyte-macrophage colony-stimulating factor in Philadelphia (Ph1)-positive acute lymphoblastic leukemia: studies on two newly established Ph1-positive acute lymphoblastic leukemia cell lines (Z-119 and Z-181).

Estrov Z, Talpaz M, Zipf TF, Kantarjian HM, Ku S, Ouspenskaia MV, Hirsch-Ginsberg C, Huh Y, Yee G, Kurzrock R.

J Cell Physiol. 1996 Mar;166(3):618-30.

PMID:
8600166
5.

Adult-onset hereditary pulmonary alveolar proteinosis caused by a single-base deletion in CSF2RB.

Tanaka T, Motoi N, Tsuchihashi Y, Tazawa R, Kaneko C, Nei T, Yamamoto T, Hayashi T, Tagawa T, Nagayasu T, Kuribayashi F, Ariyoshi K, Nakata K, Morimoto K.

J Med Genet. 2011 Mar;48(3):205-9. doi: 10.1136/jmg.2010.082586. Epub 2010 Nov 12.

PMID:
21075760
6.

Establishment of a novel human acute myeloblastic leukemia cell line (YNH-1) with t(16;21), t(1;16) and 12q13 translocations.

Yamamoto K, Hamaguchi H, Nagata K, Kobayashi M, Tanimoto F, Taniwaki M.

Leukemia. 1997 Apr;11(4):599-608.

PMID:
9096702
7.
8.

Expression of granulocyte-macrophage colony-stimulating factor receptors in human prostate cancer.

Rivas CI, Vera JC, Delgado-López F, Heaney ML, Guaiquil VH, Zhang RH, Scher HI, Concha II, Nualart F, Cordon-Cardo C, Golde DW.

Blood. 1998 Feb 1;91(3):1037-43.

9.

Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1.

Martinez-Moczygemba M, Doan ML, Elidemir O, Fan LL, Cheung SW, Lei JT, Moore JP, Tavana G, Lewis LR, Zhu Y, Muzny DM, Gibbs RA, Huston DP.

J Exp Med. 2008 Nov 24;205(12):2711-6. doi: 10.1084/jem.20080759. Epub 2008 Oct 27.

10.

A cytokine receptor gene cluster in the X-Y pseudoautosomal region?

Kremer E, Baker E, D'Andrea RJ, Slim R, Phillips H, Moretti PA, Lopez AF, Petit C, Vadas MA, Sutherland GR, et al.

Blood. 1993 Jul 1;82(1):22-8.

12.

Mapping of the human gene for inducible heme oxygenase to chromosome 22q12.

Kuwano A, Ikeda H, Takeda K, Nakai H, Kondo I, Shibahara S.

Tohoku J Exp Med. 1994 Apr;172(4):389-92.

13.
15.

Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma.

Fang JM, Arlt MF, Burgess AC, Dagenais SL, Beer DG, Glover TW.

Genes Chromosomes Cancer. 2001 Mar;30(3):292-8.

18.

Regional localization of the human platelet-derived endothelial cell growth factor (ECGF1) gene to chromosome 22q13.

Stenman G, Sahlin P, Dumanski JP, Hagiwara K, Ishikawa F, Miyazono K, Collins VP, Heldin CH.

Cytogenet Cell Genet. 1992;59(1):22-3.

PMID:
1733667
19.

Localization of the beta A4-crystallin gene (CRYBA4) on human chromosome 22 in the region q11.2-->q13.1.

van Rens GL, Geurts van Kessel AH, Bloemendal H.

Cytogenet Cell Genet. 1992;61(3):180-3.

PMID:
1424806
20.

Negative effects of GM-CSF signaling in a murine model of t(8;21)-induced leukemia.

Matsuura S, Yan M, Lo MC, Ahn EY, Weng S, Dangoor D, Matin M, Higashi T, Feng GS, Zhang DE.

Blood. 2012 Mar 29;119(13):3155-63. doi: 10.1182/blood-2011-04-350694. Epub 2012 Jan 5.

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