DOI: 10.1016/s0301-472x(01)00789-5. Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera

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

10.1016/s0301-472x(01)00789-5

Crossref journal-article

Elsevier BV

Experimental Hematology (78)

Bibliography

Kralovics, R., Guan, Y., & Prchal, J. T. (2002). Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Experimental Hematology, 30(3), 229â236.

Authors 3

Robert Kralovics (first)
Yongli Guan (additional)
Josef T Prchal (additional)

References 22 Referenced 239

10.1056/NEJM197610212951702 / N Engl J Med / Polycythemia vera by Adamson (1976)
10.1084/jem.183.2.561 / J Exp Med / Clonal stability of blood cell lineages indicated by X-chromosomal transcriptional polymorphism by Prchal (1996)
10.1016/S0025-6196(12)61011-8 / Mayo Clin Proc / Chromosome studies in 104 patients with polycythemia vera by Diez-Martin (1991)
10.1016/S0950-3536(98)80041-3 / Baillieres Clin Haematol / Molecular genetics and cytogenetics of myeloproliferative disorders by Bench (1998)
{'key': '10.1016/S0301-472X(01)00789-5_BIB5', 'first-page': '1382', 'article-title': 'Letter', 'volume': '290', 'author': 'Prchal', 'year': '1974', 'journal-title': 'N Engl J Med'} / N Engl J Med / Letter by Prchal (1974)
10.1172/JCI109003 / J Clin Invest / Polycythemia vera. The in vitro response of normal and abnormal stem cell lines to erythropoietin by Prchal (1978)
10.1182/blood.V90.2.651 / Blood / Identification of increased protein tyrosine phosphatase activity in polycythemia vera erythroid progenitor cells by Sui (1997)
10.1016/S0301-472X(99)00043-0 / Exp Hematol / Defective expression of the SHP-1 phosphatase in polycythemia vera by Wickrema (1999)
10.1056/NEJM199802263380903 / N Engl J Med / Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera (see comments) by Moliterno (1998)
10.1056/NEJM199802263380902 / N Engl J Med / Expression of bcl-x in erythroid precursors from patients with polycythemia vera by Silva (1998)
10.1182/blood.V95.8.2569 / Blood / Cloning of PRV-1, a novel member of the uPAR receptor superfamily, which is overexpressed in polycythemia rubra vera by Temerinac (2000)
10.1182/blood.V97.11.3424 / Blood / Increased expression of the INK4a/ARF locus in polycythemia vera by Dai (2001)
{'key': '10.1016/S0301-472X(01)00789-5_BIB13', 'first-page': '113a', 'article-title': 'Familial polycythemia vera', 'volume': '94', 'author': 'Kralovics', 'year': '1999', 'journal-title': 'Blood'} / Blood / Familial polycythemia vera by Kralovics (1999)
10.1172/JCI119366 / J Clin Invest / Rapid determination of clonality by detection of two closely linked X-chromosome exonic polymorphisms using allele-specific PCR by Liu (1997)
10.1002/(SICI)1096-8652(200004)63:4<184::AID-AJH4>3.0.CO;2-I / Am J Hematol / A polymorphism of the X-linked gene IDS increases the number of females informative for transcriptional clonality assays by Gregg (2000)
10.1159/000164141 / Pathobiology / Expression of five selected human mismatch repair genes simultaneously detected in normal and cancer cell lines by a nonradioactive multiplex reverse transcription polymerase chain reaction by Wei (1997)
10.1126/science.282.5397.2270 / Science / p53-independent role of MDM2 in TGF-β1 resistance by Sun (1998)
10.1182/blood.V81.1.269.269 / Blood / Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis by Prchal (1993)
10.1182/blood.V90.4.1403 / Blood / Hypermethylation of the p15INK4B gene in myelodysplastic syndromes by Uchida (1997)
{'key': '10.1016/S0301-472X(01)00789-5_BIB20', 'first-page': '3941', 'article-title': 'Two regions of deletion in 9p23-24 in sporadic breast cancer', 'volume': '59', 'author': 'An', 'year': '1999', 'journal-title': 'Cancer Res'} / Cancer Res / Two regions of deletion in 9p23-24 in sporadic breast cancer by An (1999)
10.1073/pnas.96.21.11946 / Proc Natl Acad Sci U S A / Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum by das Neves (1999)
10.1016/S0378-1119(00)00140-2 / Gene / Roles of the NFI/CTF gene family in transcription and development by Gronostajski (2000)

Dates

Type	When
Created	22 years, 10 months ago (Oct. 8, 2002, 12:02 p.m.)
Deposited	3 years, 2 months ago (June 10, 2022, 2:56 a.m.)
Indexed	17 hours, 44 minutes ago (Aug. 29, 2025, 6:18 a.m.)
Issued	23 years, 5 months ago (March 1, 2002)
Published	23 years, 5 months ago (March 1, 2002)
Published Print	23 years, 5 months ago (March 1, 2002)

Funders 0

None

BibTeX

@article{Kralovics_2002, title={Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera}, volume={30}, ISSN={0301-472X}, url={http://dx.doi.org/10.1016/s0301-472x(01)00789-5}, DOI={10.1016/s0301-472x(01)00789-5}, number={3}, journal={Experimental Hematology}, publisher={Elsevier BV}, author={Kralovics, Robert and Guan, Yongli and Prchal, Josef T}, year={2002}, month=mar, pages={229–236} }

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