Frequency of prolonged remission duration after high-dose cytarabine intensification in acute myeloid Leukemia varies by cytogenetic subtype von BLOOMFIELD, C. D, LAWRENCE, D, ARTHUR, D. C, MAYER, R. J, BYRD, J. C, CARROLL, A, PETTENATI, M. J, TANTRAVAHI, R, PATIL, S. R, DAVEY, F. R, BERG, D. T, SCHIFFER, C. A

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Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature von Tepperberg, J., Pettenati, M. J., Rao, P. N., Lese, C. M., Rita, D., Wyandt, H., Gersen, S., White, B., Schoonmaker, M. M.

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Prospective Karyotype Analysis in Adult Acute Lymphoblastic Leukemia: The Cancer and Leukemia Group B Experience von Wetzler, Meir, Dodge, Richard K., Mrózek, Krzysztof, Carroll, Andrew J., Tantravahi, Ramana, Block, AnneMarie W., Pettenati, Mark J., Beau, Michelle M. Le, Frankel, Stanley R., Stewart, Carleton C., Szatrowski, Ted P., Schiffer, Charles A., Larson, Richard A., Bloomfield, Clara D.

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Identification of a Mutation in DLX3 Associated with Tricho-Dento-Osseous (TDO) Syndrome von Price, Jennifer A., Bowden, Donald W., Tim Wright, J., Pettenati, Mark J., Hart, Thomas C.

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The HA-2 Minor Histocompatibility Antigen Is Derived from a Diallelic Gene Encoding a Novel Human Class I Myosin Protein von Pierce, Richard A, Field, Erin D, Mutis, Tuna, Golovina, Tatiana N, Kap-Herr, Chris Von, Wilke., Martina, Pool, Jos, Shabanowitz, Jeffrey, Pettenati, Mark J, Eisenlohr, Laurence C, Hunt, Donald F, Goulmy, Els, Engelhard, Victor H

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Secondary cytogenetic changes in acute promyelocytic leukemia--prognostic importance in patients treated with chemotherapy alone and association with the intron 3 breakpoint of the... von SLACK, J. L, ARTHUR, D. C, RAO, K. W, SCHIFFER, C. A, BLOOMFIELD, C. D, LAWRENCE, D, MROZEK, K, MAYER, R. J, DAVEY, F. R, TANTRAVAHI, R, PETTENATI, M. J, BIGNER, S, CARROLL, A. J

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Ring chromosome 17: phenotype variation by deletion size von Shashi, V, White, JR, Pettenati, MJ, Root, SK, Bell, WL

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Detection of Abnormal Pretransplant Clones in Progenitor Cells of Patients Who Developed Myelodysplasia After Autologous Transplantation von Abruzzese, Elisabetta, Radford, James E., Miller, Jeffrey S., Vredenburgh, James J., Rao, P. Nagesh, Pettenati, Mark J., Cruz, Julia M., Perry, James J., Amadori, Sergio, Hurd, David D.

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Genetic Linkage of Hereditary Gingival Fibromatosis to Chromosome 2p21 von Hart, Thomas C., Pallos, Debora, Bowden, Donald W., Bolyard, Joey, Pettenati, Mark J., Cortelli, Jose R.

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Structure, alternative splicing, and expression of the human RGS9 gene von Zhang, K., Howes, K.A., He, W., Bronson, J.D., Pettenati, M.J., Chen, C.-K., Palczewski, K., Wensel, T.G., Baehr, W.

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Patients with isolated trisomy 8 in acute myeloid leukemia are not cured with cytarabine-based chemotherapy: results from Cancer and Leukemia Group B 8461 von BYRD, J. C, LAWRENCE, D, ARTHUR, D. C, PETTENATI, M. J, TANTRAVAHI, R, QUMSIYEH, M, STAMBERG, J, DAVEY, F. R, SCHIFFER, C. A, BLOOMFIELD, C. D

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Identification of a human gene (HCK) that encodes a protein-tyrosine kinase and is expressed in hemopoietic cells von QUINTRELL, N, LEBO, R, VARMUS, H, BISHOP, J. M, PETTENATI, M. J, LE BEAU, M. M, DIAZ, M. O, ROWLEY, J. D

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Fatal EBV-related post-transplant lymphoproliferative disorder (LPD) after matched related donor nonmyeloablative peripheral blood progenitor cell transplant von Zamkoff, K W, Bergman, S, Beaty, M W, Buss, D H, Pettenati, M J, Hurd, D D

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Genetic heterogeneity of gingival fibromatosis on chromosome 2p von Shashi, Vandana, Pallos, Debora, Pettenati, Mark J, Cortelli, Jose R, Fryns, Jean-Pierre, von Kap-Herr, Christopher, Hart, Thomas C

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Primary malignant lymphoma of uterine corpus: case report and review of the literature von RENNO, S. I, MORELAND, W. S, PETTENATI, M. J, BEATY, M. W, KEUNG, Y.-K

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Down syndrome congenital heart disease: A narrowed region and a candidate gene von Barlow, Gillian M, Chen, Xiao-Ning, Shi, Zheng Y, Lyons, Gary E, Kurnit, David M, Celle, Livija, Spinner, Nancy B, Zackai, Elaine, Pettenati, Mark J, Van Riper, Alexander J, Vekemans, Michael J, Mjaatvedt, Corey H, Korenberg, Julie R

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The human NACP/α-synuclein gene: chromosome assignment to 4q21.3–q22 and TaqI RFLP analysis von Chen, Xiaohua, de Silva, H.A.Rohan, Pettenati, Mark J., Rao, P.Nagesh, George-Hyslop, Peter St, Roses, Allen D., Xia, Yu, Horsburgh, Karen, Uéda, Kenji, Saitoh, Tsunao

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Assignment of CSF-1 to 5q33.1: Evidence for Clustering of Genes Regulating Hematopoiesis and for Their Involvement in the Deletion of the Long Arm of Chromosome 5 in Myeloid Disord... von Pettenati, Mark J., Le Beau, Michelle M., Lemons, Richard S., Shima, Elizabeth A., Kawasaki, Ernest S., Larson, Richard A., Sherr, Charles J., Diaz, Manuel O., Rowley, Janet D.

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Comparison of Cytogenetic and Molecular Genetic Detection of t(8;21) and inv(16) in a Prospective Series of Adults With De Novo Acute Myeloid Leukemia: A Cancer and Leukemia Group... von MROZEK, Krzysztof, PRIOR, Thomas W, CALIGIURI, Michael A, VARDIMAN, James W, KOLITZ, Jonathan E, LARSON, Richard A, BLOOMFIELD, Clara D, EDWARDS, Colin, MARCUCCI, Guido, CARROLL, Andrew J, SNYDER, Pamela J, KODURU, Prasad R. K, THEIL, Karl S, PETTENATI, Mark J, ARCHER, Kellie J

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The human cornea has a high incidence of acquired chromosome abnormalities von PETTENATI, M. J, SWEATT, A. J, LANTZ, P, STANTON, C. A, REYNOLDS, J, NAGESH RAO, P, DAVIS, R. M

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