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Maria Proytcheva, MD
Assistant Professor of Pathology
Director, Hematology Laboratories
CMH
Box 17
2300 Children's Plaza
Chicago, IL 60614
mproytcheva@childrensmemorial.org
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Phone: (773 )880-3985
Fax: (773) 880-8127
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Anatomic Pathology Division
Autopsy
Sub-specialty Hematology, Sub-specialty Transfusion Medicine
Clinical Pathology
Blood Bank
Hemostasis-Coagulation
Hematopathology
Flow Cytometry
Medical School
Higher Medical Institute, Medical University, Sofia, Bulgaria, 1983
Site of Residency
Albert Einstein College of Medicine, 2001
Site of Fellowship
Yale University School of Medicine, 2003
/ Weill Medical College at Cornell University, 2002
Research Interests
Hematology, Transfusion Medicine
Selected Publications
 Ellis,
N. A., Roe, A. M., Kozloski, J., Proytcheva, M., Falk, C., and
German, J.: Linkage disequilibrium between the FES, D15S127, and BLM loci
in Ashkenazi Jews with Bloom's syndrome. Amer. J. Hum. Genet. 55:450-460, 1994.
Ellis,
N. A., Lennon, D. J., Proytcheva, M., Alhadeff, B., Henderson,
E. E., and German, J.: Somatic intragenic recombination within the mutated
locus BLM can correct the high-SCE phenotype of Bloom syndrome cells. Amer. J.
Hum. Genet., 57:1019-1027, 1995 .
Ellis,
N. A., Groden, J., Ye, T.-Z., Straughen,J., Lennon, D. J., Ciocci, S., Proytcheva,
M., and German, J.: The Bloom's syndrome gene product is homologous
to RecQ helicases. Cell, 83:655-666, 1995.
Straughen,
J., Ciocci, S., Ye, T.-Z., Lennon, D. J., Alhadeff, B., Proytcheva, M.,
Goodfellow, P., German, J. Ellis, N. A., and Groden, J.: Physical mapping
of the Bloom's syndrome region by the identification of YAC and P1 clones from
human chromosome 15 band q26.1. Genomics, 35, 118-128, 1996.
German,
J., Ellis, N. A., and Proytcheva, M.: Bloom's syndrome.
XIX. Cytogenetic and population evidence for genetic heterogeneity. Clinical Genetics,
49: 223-231, 1996 .
Straughen,
J.E., Johnson, J., McLaren, D., Proytcheva, M., Ellis, N., German,
J., and Groden, J.: A rapid method for detecting the predominant Ashkenazi
Jewish mutation in the Bloom’s syndrome gene. Human Mutation 11:175-178,
1998.
Ellis,
N., Ciocci, S., Proytcheva, M., Lennon, D., Groden, J., and German,
J.: The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish
Americans of Spanish ancestry. Amer. J. Hum. Genet. 63: 1685-1693, 1998.
Neff,
N. F., Ellis, N., Ye, T. Z., Noonan, J., Huang, K., Sanz, M., and Proytcheva,
M.: The DNA helicase activity of the BLM is necessary for the correction
of the genomic instability for Bloom syndrome cells. Mol. Biol. Cell, 10:665-676,
1999.
Ellis,
N. A., Proytcheva, M., Sanz, M., Ye, T. Z. and German, J.:
Transfection of BLM into cultured Bloom syndrome cells reduces the SCE rate toward
normal. Amer. J. Hum. Genets.65:1368-1374, 1999.
Sanz,
M.M., Proytcheva, M., Ellis. N.A., Holloman, W.K., and German,
J.L.: BLM, the Bloom's syndrome protein, varies during the cell cycle in
its amount, distribution, and co-localization with other nuclear proteins. Cytogenet.
Cell Genet. 91:217-223, 2000.
Mechanic,
S., Krause, D.S., Proytcheva, M., Snyder, E.L. Mobilization
and collection of peripheral blood progenitor cells. In: Apheresis: Principle
and Practice, Second edition, Bethesda, MD AABB Press: 503-530, 2003.
Recommended Resources
American Society of Hematology, Society for Hematopathology, American Society of Clinical Pathology, American Association of Blood Banks
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