Search Results - "Pettenati, M."

Sixty years of global progress in managed aquifer recharge by Dillon, P., Stuyfzand, P., Grischek, T., Lluria, M., Pyne, R. D. G., Jain, R. C., Bear, J., Schwarz, J., Wang, W., Fernandez, E., Stefan, C., Pettenati, M., van der Gun, J., Sprenger, C., Massmann, G., Scanlon, B. R., Xanke, J., Jokela, P., Zheng, Y., Rossetto, R., Shamrukh, M., Pavelic, P., Murray, E., Ross, A., Bonilla Valverde, J. P., Palma Nava, A., Ansems, N., Posavec, K., Ha, K., Martin, R., Sapiano, M.

“…The last 60 years has seen unprecedented groundwater extraction and overdraft as well as development of new technologies for water treatment that together…”
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Transfer of trace organic compounds in an operational soil-aquifer treatment system assessed through an intrinsic tracer test and transport modelling by Guillemoto, Q., Picot-Colbeaux, G., Valdes, D., Devau, N., Mathurin, F.A., Pettenati, M., Kloppmann, W., Mouchel, J.-M.

“…Soil Aquifer Treatment (SAT) can provide supplementary treatment of trace organic compounds (TrOCs) such as pharmaceutical and industrial compounds present in…”
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Investigation of recharge dynamics and flow paths in a fractured crystalline aquifer in semi-arid India using borehole logs: implications for managed aquifer recharge by Alazard, M, Boisson, A, Maréchal, J-C, Perrin, J, Dewandel, B, Schwarz, T, Pettenati, M, Picot-Colbeaux, G, Kloppman, W, Ahmed, S

“…The recharge flow paths in a typical weathered hard-rock aquifer in a semi-arid area of southern India were investigated in relation to structures associated…”
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Short-term assessment of the dynamics of elements in wastewater irrigated Mediterranean soil and tomato fruits through sequential dissolution and lead isotopic signatures by Cary, L., Surdyk, N., Psarras, G., Kasapakis, I., Chartzoulakis, K., Sandei, L., Guerrot, C., Pettenati, M., Kloppmann, W.

“…•A geochemical approach was used to investigate wastewater irrigated soil and crop quality.•Specific drip irrigation can lead to localized metals accumulation…”
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Frequency of prolonged remission duration after high-dose cytarabine intensification in acute myeloid Leukemia varies by cytogenetic subtype by 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

“…Advances in the treatment of acute myeloid leukemia (AML) have occurred with the introduction of new therapies including high-dose cytarabine and the…”
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Prospective Karyotype Analysis in Adult Acute Lymphoblastic Leukemia: The Cancer and Leukemia Group B Experience by 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.

“…The Cancer and Leukemia Group B (CALGB) has been conducting a prospective cytogenetic companion study (CALGB 8461) to all CALGB treatment protocols for newly…”
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Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature by Tepperberg, J., Pettenati, M. J., Rao, P. N., Lese, C. M., Rita, D., Wyandt, H., Gersen, S., White, B., Schoonmaker, M. M.

“…Since 1993, the position of the American College of Medical Genetics (ACMG) has been that prenatal interphase fluorescence in situ hybridization (FISH) is…”
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Identification of a Mutation in DLX3 Associated with Tricho-Dento-Osseous (TDO) Syndrome by Price, Jennifer A., Bowden, Donald W., Tim Wright, J., Pettenati, Mark J., Hart, Thomas C.

“…Tricho-dento-osseous syndrome (TDO) is an autosomal dominant disorder characterized by abnormal hair, teeth and bone. The main clinical manifestations of TDO…”
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Impact of irrigation with treated low quality water on the heavy metal contents of a soil-crop system in Serbia by Surdyk, N., Cary, L., Blagojevic, S., Jovanovic, Z., Stikic, R., Vucelic-Radovic, B., Zarkovic, B., Sandei, L., Pettenati, M., Kloppmann, W.

“…Water availability for irrigation is a limiting factor for agriculture in Mediterranean countries. An upcoming strategy for increasing water supply is to use…”
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Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study by Graf, M D, Christ, L, Mascarello, J T, Mowrey, P, Pettenati, M, Stetten, G, Storto, P, Surti, U, Van Dyke, D L, Vance, G H, Wolff, D, Schwartz, S

“…Background: A marker chromosome is defined as a structurally abnormal chromosome that cannot be identified by routine cytogenetics. The risk for phenotypic…”
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The HA-2 Minor Histocompatibility Antigen Is Derived from a Diallelic Gene Encoding a Novel Human Class I Myosin Protein by 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

“…Human minor histocompatibility Ags (mHag) present significant barriers to successful bone marrow transplantation. However, the structure of human mHag and the…”
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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 PML gene: a Cancer and Leukemia Group B study by Slack, J L, Arthur, D C, Lawrence, D, Mrózek, K, Mayer, R J, Davey, F R, Tantravahi, R, Pettenati, M J, Bigner, S, Carroll, A J, Rao, K W, Schiffer, C A, Bloomfield, C D

“…To examine, in newly diagnosed patients with acute promyelocytic leukemia (APL), the prognostic significance of secondary cytogenetic changes and the…”
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Ring chromosome 17: phenotype variation by deletion size by Shashi, V, White, JR, Pettenati, MJ, Root, SK, Bell, WL

“…Ring chromosome 17 is a rare cytogenetic abnormality, with 12 previous reports in the literature. Some have a relatively mild phenotype characterized by…”
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Detection of Abnormal Pretransplant Clones in Progenitor Cells of Patients Who Developed Myelodysplasia After Autologous Transplantation by 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.

“…Secondary myelodysplastic syndromes (MDS) have been reported after autologous transplantation. It is not known whether the MDS results from the pretransplant…”
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Structure, alternative splicing, and expression of the human RGS9 gene by Zhang, K., Howes, K.A., He, W., Bronson, J.D., Pettenati, M.J., Chen, C.-K., Palczewski, K., Wensel, T.G., Baehr, W.

“…An isoform of RGS9 was recently identified as the GTPase activating protein in bovine and mouse rod and cone photoreceptors. To explore the potential role of…”
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Genetic Linkage of Hereditary Gingival Fibromatosis to Chromosome 2p21 by Hart, Thomas C., Pallos, Debora, Bowden, Donald W., Bolyard, Joey, Pettenati, Mark J., Cortelli, Jose R.

“…Gingival fibromatosis is characterized by a slowly progressive benign enlargement of the oral gingival tissues. The condition results in the teeth being…”
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Primary malignant lymphoma of uterine corpus: case report and review of the literature by RENNO, S. I, MORELAND, W. S, PETTENATI, M. J, BEATY, M. W, KEUNG, Y.-K

“…We describe a patient presenting with postmenopausal vaginal bleeding and a uterine mass subjected to endometrial biopsy that showed a high-grade non-Hodgkin's…”
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Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndrome by Zhang, Y., Hart, P.S., Moretti, A.J., Bouwsma, O.J., Fisher, E.M., Dudlicek, L., Pettenati, M.J., Hart, T.C.

“…Papillon Lefèvre syndrome (PLS) is an autosomal recessive disorder characterized by palmoplantar hyperkeratosis and severe periodontitis. The disease is caused…”
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Genetic heterogeneity of gingival fibromatosis on chromosome 2p by Shashi, Vandana, Pallos, Debora, Pettenati, Mark J, Cortelli, Jose R, Fryns, Jean-Pierre, von Kap-Herr, Christopher, Hart, Thomas C

“…Gingival fibromatosis (GF) occurs in several genetic forms as a simple Mendelian trait, in malformation syndromes, and in some chromosomal disorders. Specific…”
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Fatal EBV-related post-transplant lymphoproliferative disorder (LPD) after matched related donor nonmyeloablative peripheral blood progenitor cell transplant by ZAMKOFF, K. W, BERGMAN, S, BEATY, M. W, BUSS, D. H, PETTENATI, M. J, HURD, D. D

“…A 39-year-old male underwent a nonmyeloablative stem cell transplant (NMAPBPCT) from his HLA-matched sister for recurrent anaplastic large cell lymphoma in…”
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