Guan Y - Search Results

1

Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.

Mims MP, Guan Y, Pospisilova D, Priwitzerova M, Indrak K, Ponka P, Divoky V, Prchal JT. Mims MP, et al. Among authors: guan y. Blood. 2005 Feb 1;105(3):1337-42. doi: 10.1182/blood-2004-07-2966. Epub 2004 Sep 30. Blood. 2005. PMID: 15459009 Free article.

2

Mutations in the VHL gene in sporadic apparently congenital polycythemia.

Pastore YD, Jelinek J, Ang S, Guan Y, Liu E, Jedlickova K, Krishnamurti L, Prchal JT. Pastore YD, et al. Among authors: guan y. Blood. 2003 Feb 15;101(4):1591-5. doi: 10.1182/blood-2002-06-1843. Epub 2002 Oct 10. Blood. 2003. PMID: 12393546 Free article.

3

Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietin.

Liu E, Jelinek J, Pastore YD, Guan Y, Prchal JF, Prchal JT. Liu E, et al. Among authors: guan y. Blood. 2003 Apr 15;101(8):3294-301. doi: 10.1182/blood-2002-07-2287. Epub 2002 Dec 19. Blood. 2003. PMID: 12515724 Free article.

4

The worldwide distribution of the VHL 598C>T mutation indicates a single founding event.

Liu E, Percy MJ, Amos CI, Guan Y, Shete S, Stockton DW, McMullin MF, Polyakova LA, Ang SO, Pastore YD, Jedlickova K, Lappin TR, Gordeuk V, Prchal JT. Liu E, et al. Among authors: guan y. Blood. 2004 Mar 1;103(5):1937-40. doi: 10.1182/blood-2003-07-2550. Epub 2003 Nov 6. Blood. 2004. PMID: 14604959 Free article.

5

Primary familial polycythemia: a frameshift mutation in the erythropoietin receptor gene and increased sensitivity of erythroid progenitors to erythropoietin.

Sokol L, Luhovy M, Guan Y, Prchal JF, Semenza GL, Prchal JT. Sokol L, et al. Among authors: guan y. Blood. 1995 Jul 1;86(1):15-22. Blood. 1995. PMID: 7795221 Free article.

6

Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera.

Kralovics R, Guan Y, Prchal JT. Kralovics R, et al. Among authors: guan y. Exp Hematol. 2002 Mar;30(3):229-36. doi: 10.1016/s0301-472x(01)00789-5. Exp Hematol. 2002. PMID: 11882360 Free article.

7

High levels of circulating CD34 cells, dacrocytes, clonal hematopoiesis, and JAK2 mutation differentiate myelofibrosis with myeloid metaplasia from secondary myelofibrosis associated with pulmonary hypertension.

Popat U, Frost A, Liu E, Guan Y, Durette A, Reddy V, Prchal JT. Popat U, et al. Among authors: guan y. Blood. 2006 May 1;107(9):3486-8. doi: 10.1182/blood-2005-08-3319. Epub 2006 Jan 17. Blood. 2006. PMID: 16418333 Free article.

8

A novel clonality assay based on transcriptional analysis of the active X chromosome.

Prchal JT, Guan YL. Prchal JT, et al. Among authors: guan yl. Stem Cells. 1993 May;11 Suppl 1:62-5. doi: 10.1002/stem.5530110613. Stem Cells. 1993. PMID: 8318921

9

Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.

Ang SO, Chen H, Hirota K, Gordeuk VR, Jelinek J, Guan Y, Liu E, Sergueeva AI, Miasnikova GY, Mole D, Maxwell PH, Stockton DW, Semenza GL, Prchal JT. Ang SO, et al. Among authors: guan y. Nat Genet. 2002 Dec;32(4):614-21. doi: 10.1038/ng1019. Epub 2002 Nov 4. Nat Genet. 2002. PMID: 12415268

10

Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis.

Prchal JT, Guan YL, Prchal JF, Barany F. Prchal JT, et al. Among authors: guan yl. Blood. 1993 Jan 1;81(1):269-71. Blood. 1993. PMID: 8093348 Free article. No abstract available.

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