Search Results - "Sahoo, Sangita"

Unravelling a bench-stable zinc-amide compound as highly active multitasking catalyst for radical-mediated selective alk(en)ylation of unactivated carbocycles under mild conditions by Sahoo, Sangita, Manna, Subarna, Rit, Arnab

“…The direct functionalization of unactivated organic moieties via C-C bond formation has long fascinated synthetic chemists. Although base-metal systems are…”
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Simple silver(I)-salt catalyzed selective hydroboration of isocyanates, pyridines, and quinolines by Pandey, Vipin K, Sahoo, Sangita, Rit, Arnab

“…AgSbF has been established as an effective catalyst for the hydroboration of structurally and electronically diverse isocyanates under ligand- and solvent-free…”
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Combined effects of elevated CO2, N fertilizer and water deficit stress on diazotrophic community in sub-humid tropical paddy soil by Kumar, Upendra, Nayak, A.K., Sahoo, Sangita, Kumar, A., Kaviraj, Megha, Shahid, M.

“…Elevated carbon dioxide (eCO2), higher dose of recommended nitrogen (HDN), and water deficit stress (WDS) are three important factors which influence…”
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Clinical and Molecular Heterogeneity of RTEL1 Deficiency by Speckmann, Carsten, Sahoo, Sushree Sangita, Rizzi, Marta, Hirabayashi, Shinsuke, Karow, Axel, Serwas, Nina Kathrin, Hoemberg, Marc, Damatova, Natalja, Schindler, Detlev, Vannier, Jean-Baptiste, Boulton, Simon J, Pannicke, Ulrich, Göhring, Gudrun, Thomay, Kathrin, Verdu-Amoros, J J, Hauch, Holger, Woessmann, Wilhelm, Escherich, Gabriele, Laack, Eckart, Rindle, Liliana, Seidl, Maximilian, Rensing-Ehl, Anne, Lausch, Ekkehart, Jandrasits, Christine, Strahm, Brigitte, Schwarz, Klaus, Ehl, Stephan R, Niemeyer, Charlotte, Boztug, Kaan, Wlodarski, Marcin W

“…Typical features of dyskeratosis congenita (DC) resulting from excessive telomere shortening include bone marrow failure (BMF), mucosal fragility, and…”
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Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency by Speckmann, Carsten, Sahoo, Sushree Sangita, Rizzi, Marta, Hirabayashi, Shinsuke, Karow, Axel, Serwas, Nina Kathrin, Hoemberg, Marc, Damatova, Natalja, Schindler, Detlev, Vannier, Jean-Baptiste, Boulton, Simon J, Pannicke, Ulrich, Göhring, Gudrun, Thomay, Kathrin, Verdu-Amoros, J J, Hauch, Holger, Woessmann, Wilhelm, Escherich, Gabriele, Laack, Eckart, Rindle, Liliana, Seidl, Maximilian, Rensing-Ehl, Anne, Lausch, Ekkehart, Jandrasits, Christine, Strahm, Brigitte, Schwarz, Klaus, Ehl, Stephan R, Niemeyer, Charlotte, Boztug, Kaan, Wlodarski, Marcin W

“…[This corrects the article on p. 449 in vol. 8, PMID: 28507545.]…”
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Germline SAMD9/9L MDS Predisposition Syndromes Are Characterized By Complex Clonal Architecture and Lineage-Specific Escape Mechanisms Including Somatic Genetic Rescue in T and B Lymphocytes by Goodings-Harris, Charnise, Sahoo, Sushree Sangita, Lewis, Sara, Kozyra, Emilia J., Arribas-Layton, Marc, Ramamoorthy, Senthilkumar, Jesudas, Rohith, Gray, Nathan, Erlacher, Miriam, Niemeyer, Charlotte M., Wlodarski, Marcin W

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Germline Gain-of-Function JAK3 Mutation in Familial Chronic Lymphoproliferative Disorder of NK Cells by Lesmana, Harry, Popescu, Marcela, Lewis, Sara, Sahoo, Sushree Sangita, Goodings-Harris, Charnise, Onciu, Mihaela, Choi, John Kim, Takemoto, Clifford, Nichols, Kim E., Wlodarski, Marcin

“…Chronic lymphoproliferative disorder of NK-cells (CLPD-NK) predominantly occurs in adults with a median age of diagnosis at 60 years. It is characterized by a…”
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RPA1 Gain of Function Causes Human Short Telomere Syndrome with Revertant Somatic Mosaicism by Sharma, Richa, Sahoo, Sushree Sangita, Honda, Masayoshi, Goodings-Harris, Charnise, Pastor, Victor, Busch, Hauke, Börries, Melanie, Beier, Fabian, Erlacher, Miriam, Lauten, Melchior, Wold, Marc, Spies, Maria, Niemeyer, Charlotte M., Wlodarski, Marcin

“…Dyskeratosis congenita (DC) is a short telomere syndrome with bone marrow failure (BMF), mucocutaneous fragility and predisposition to malignancy due to…”
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Prevalence of Inherited Predisposition Syndromes in Young Patients with Acute Myeloid Leukemia and Aberrant Karyotype by Kirschner, Martin, Rolles, Benjamin, Crysandt, Martina, Röllig, Christoph, Stolzel, Friedrich, Bornhäuser, Martin, Müller-Tidow, Carsten, Kricheldorf, Kim, Vieri, Margherita, Begemann, Matthias, Maurer, Angela, Panse, Jens, Isfort, Susanne, Wlodarski, Marcin, Sahoo, Sushree Sangita, Brümmendorf, Tim H, Jost, Edgar, Beier, Fabian

“…Introduction Recent studies indicate that particularly in a subgroup of younger patients, acute myeloid leukemia (AML) develops due to an inherited genetic…”
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5-Azacytidine Is Effective for Targeting Leukemia-Initiating Cells in Juvenile Myelomonocytic Leukemia by Krombholz, Christopher Felix, Gallego Villar, Lorena, Panda, Pritam Kumar, Sahoo, Sushree Sangita, Wlodarski, Marcin W., Lipka, Daniel B., Plass, Christoph, Niemeyer, Charlotte, Erlacher, Miriam, Flotho, Christian

“…Juvenile myelomonocytic leukemia (JMML) is a myeloproliferative neoplasm of young children that originates from early hematopoietic stem/progenitor cells. We…”
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Monosomy 7 As the Initial Hit Followed By Sequential Acquisition of SETBP1 and ASXL1 Driver Mutations in Childhood Myelodysplastic Syndromes by Pastor Loyola, Victor, Panda, Pritam Kumar, Sahoo, Sushree Sangita, Szvetnik, Enikoe Amina, Kozyra, Emilia J., Voss, Rebecca K, Lebrecht, Dirk, Wehrle, Julius, Erlacher, Miriam, Stary, Jan, Flotho, Christian, Göhring, Gudrun, Schlegelberger, Brigitte, Strahm, Brigitte, Niemeyer, Charlotte, Wlodarski, Marcin W.

“…Childhood myelodysplastic syndromes (MDS) account for less than 5% of pediatric hematologic malignancies and differ from their adult counterpart in terms of…”
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Cholera toxin-B (ctxB) antigen expressing Salmonella Typhimurium polyvalent vaccine exerts protective immune response against Vibrio cholerae infection by Vishwakarma, Vikalp, Sahoo, Sushree Sangita, Das, Susmita, Ray, Shilpa, Hardt, Wolf-Dietrich, Suar, Mrutyunjay

“…Highlights • Live attenuated Salmonella Typhimurium vaccine (Z234-pMS101) was developed against Salmonellosis and Cholera infection. • Heterologous antigen…”
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SAMD9 and SAMD9L Germline Disorders in Patients Enrolled in Studies of the European Working Group of MDS in Childhood (EWOG-MDS): Prevalence, Outcome, Phenotype and Functional Characterisation by Sahoo, Sushree Sangita, Pastor Loyola, Victor, Panda, Pritam Kumar, Szvetnik, Enikoe Amina, Kozyra, Emilia J., Voss, Rebecca K, Lebrecht, Dirk, Barzilai, Shlomit, Büchner, Jochen, Catala, Albert, De Moerloose, Barbara, Dworzak, Michael, Fabri, Oksana, Hasle, Henrik, Jahnukainen, Kirsi, Kállay, Krisztián, Locatelli, Franco, Masetti, Riccardo, Polychronopoulou, Sophia, Schmugge, Markus, Stary, Jan, Smith, Owen P, Turkiewicz, Dominik, Ussowicz, Marek, van den Heuvel-Eibrink, Marry M., Noellke, Peter, Göhring, Gudrun, Erlacher, Miriam, Flotho, Christian, Strahm, Brigitte, Niemeyer, Charlotte, Wlodarski, Marcin W.

“…▪ Hereditary predisposition has been ever since implicated in the etiology of childhood myelodysplastic syndromes (MDS). Until recently, GATA2 deficiency…”
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Functional Consequences of TCAB1 Mutations in Dyskeratosis Congenita by Sahoo, Sushree Sangita, Roake, Caitlin, Rindle, Liliana, Rössig, Claudia, Schmugge, Markus, Pastor, Victor B, Strahm, Brigitte, Niewisch, Marena R, Ruzaike, Gunda, Artandi, Steven, Niemeyer, Charlotte M, Börries, Melanie, Busch, Hauke, Wlodarski, Marcin

“…Dyskeratosis congenita (DC) is a rare telomere disease with pleiotropic manifestations and bone marrow failure (BMF) as a major cause of mortality. The genes…”
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Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations by Kozyra, Emilia J, Pastor Loyola, Victor, Wehr, Claudia, Sahoo, Sushree Sangita, Voss, Rebecca, Szvetnik, Enikoe Amina, Hirabayashi, Shinsuke, Catala, Albert, Hasle, Henrik, Van den Heuvel-Eibrink, Marry M., Kallay, Krisztián, Masetti, Riccardo, De Moerloose, Barbara, Schmugge, Markus, Smith, Owen, Ussowicz, Marek, Stary, Jan, Mejstrikova, Ester, Pasaulienė, Ramunė, Baumann, Irith, Göhring, Gudrun, Schlegelberger, Brigitte, Salzer, Ulrich, Lübbert, Michael, Trompouki, Eirini, Niemeyer, Charlotte M., Wlodarski, Marcin W.

“…Among its different clinical presentations, GATA2 deficiency had been recognized as the most frequent hereditary predisposition to pediatric myelodysplastic…”
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Constitutional SAMD9L Mutations Cause Familial Myelodisplastic Syndrome with Monosomy 7 and Stable Revertant Mosaicism by Pastor Loyola, Victor, Sahoo, Sushree Sangita, Boklan, Jessica, Schwabe, Georg, Strahm, Brigitte, Lebrecht, Dirk, Voss, Matthias, Bryceson, Yenan T, Erlacher, Miriam, Ehninger, Gerhard, Niewisch, Marena, Schlegelberger, Brigitte, Baumann, Irith, Achermann, John, Shimamura, Akiko, Hochrein, Jochen, Tedgaard, Ulf, Nilsson, Lars, Hasle, Henrik, Börries, Melanie, Busch, Hauke, Niemeyer, Charlotte M., Wlodarski, Marcin W.

“…Familial myelodysplastic syndromes (MDS) arise from haploinsufficiency of genes involved in hematopoiesis, show variable penetrance and are primarily…”
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Diamond-Blackfan Anemia Phenotype Caused By Deficiency of Adenosine Deaminase 2 by Szvetnik, Enikoe Amina, Klemann, Christian, Hainmann, Ina, O'-Donohue, Marie-Francoise, Farkas, Tamás, Niewisch, Marena, Grosse, Regine, Escherich, Gabriele, Unal, Sule, Guleray, Naz, Gokce, Muge, Da Costa, Lydie, LeBlanc, Thierry, Dollfus, Hélène, Lara-Villacanas, Eusebia, Wiesel, Thomas, Pastor Loyola, Victor, Sahoo, Sushree Sangita, Steinemann, Doris, Lorenz, Myriam, Schwarz, Klaus, Ehl, Stephan, Hershfield, Michael, Gleizes, Pierre-Emmanuel, Niemeyer, Charlotte M., MacInnes, Alyson W., Wlodarski, Marcin W.

“…Diamond-Blackfan anemia (DBA) is a prototypic ribosomopathy and remains the most common cause of congenital pure red cell aplasia (PRCA). In 2/3 of patients,…”
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