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Tìm được 49 kết quả
Research progress on gene mutations and drug resistance in leukemia
Tác giả: Xiangyu Ma, Jiamin Xu, Libo Zhao, Yanan Wang, Joshua S Fleishman, Hao Bing, Boran Yu, Yanming Li, Letao Bo, Shaolong Zhang, Zhe-Sheng Chen
Xuất bản: Scotland: Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy , 2025
Bộ sưu tập: NCBI
ddc:  784.190288
 
Novel recurrent mutations and genetic diversity in Sudanese children with Adrenal Insufficiency
Tác giả: Salwa A Musa, Mohamed A Abdullah, Saptarshi Maitra, Areej A Ibrahim, Younus Qamar, Avinaash V Maharaj, Lucia M Marroquin Ramirez, Jordan Read, Li F Chan, Louise A Metherell, Chris J Smith, Samar S Hassan, Luqman S Fauzi, Omer O Babiker, Amna I Ahmed, Marwa Mohammedali, Claire Hutchison, Ghassan Mohamadsalih, Charlotte L Hall
Xuất bản: England: European journal of endocrinology , 2025
Bộ sưu tập: NCBI
ddc:  978.02
 
Impact of myelodysplasia-related and additional gene mutations in intensively treated patients with
Tác giả: Sibylle Cocciardi, Maral Saadati, Michael W M Kühn, Ulrich Germing, Karin T Mayer, Michael Lübbert, Elli Papaemmanuil, Felicitas Thol, Michael Heuser, Arnold Ganser, Lars Bullinger, Axel Benner, Nina Weiß, Hartmut Döhner, Konstanze Döhner, Daniela Späth, Silke Kapp-Schwoerer, Isabelle Schneider, Annika Meid, Verena I Gaidzik, Sabrina Skambraks, Walter Fiedler
Xuất bản: United States: HemaSphere , 2025
Bộ sưu tập: NCBI
ddc:  784.190287
 
Mutations in TAC1B drive CDR1 and MDR1 expression and azole resistance in C. auris
Tác giả: Katherine S Barker, Darian J Santana, Qing Zhang, Tracy L Peters, Jeffrey Rybak, Joachim Morschhauser, Christina A Cuomo, P David Rogers
Xuất bản: United States: bioRxiv : the preprint server for biology , 2025
Bộ sưu tập: NCBI
ddc:  636.7538
 
Detection of PRKAR1A gene mutations in sporadic cardiac myxomas: a study of 24 cases
Tác giả: Elise Bekers, Diede A G van Bladel, Madeleine R Berendsen, Astrid Eijkelenboom, J Han J M van Krieken, Marc Ooft, Emiel Ruijter, Ad Verhagen, Uta E Flucke, Blanca Scheijen
Xuất bản: Germany: Virchows Archiv : an international journal of pathology , 2025
Bộ sưu tập: NCBI
ddc:  149.2
 
Identification of novel biallelic mutations in CFAP53 associated with fetal situs inversus totalis and literature review
Tác giả: Zhenglong Guo, Mengyao Tan, Shixiu Liao, Hongjie Zhu, Guiyu Lou, Xiaoliang Xia, Wenke Yang, Yibing Lv, Jianmei Huang, Ruili Wang, Bingtao Hao
Xuất bản: England: Journal of applied genetics , 2025
Bộ sưu tập: NCBI
ddc:  636.0885
 
Mutations in hnRNP A1 drive neurodegeneration and alternative RNA splicing of neuronal gene targets
Tác giả: Ansalna Ansari, Patricia A Thibault, Hannah E Salapa, Joseph-Patrick W E Clarke, Michael C Levin
Xuất bản: United States: Neurobiology of disease , 2025
Bộ sưu tập: NCBI
ddc:  912.01
 
The mosaicism of Cas-induced mutations and pleiotropic effects of scarlet gene in an emerging model system
Tác giả: Sen Xu, Swatantra Neupane, Hongjun Wang, Thinh Phu Pham, Marelize Snyman, Trung V Huynh, Li Wang
Xuất bản: England: Heredity , 2025
Bộ sưu tập: NCBI
ddc:  305.568
 
Mutations in the Bone Morphogenetic Protein signaling pathway sensitize zebrafish and humans to ethanol-induced jaw malformations
Tác giả: John R Klem, Tae-Hwi Schwantes-An, Marco Abreu, Michael Suttie, Raeden Gray, Hieu Vo, Grace Conley, Tatiana M Foroud, Leah Wetherill, C Ben Lovely
Xuất bản: England: Disease models & mechanisms , 2025
Bộ sưu tập: NCBI
ddc:  949.59012
 
Identification of new candidate drugs in myelodysplastic syndromes with splicing factor mutations by transcriptional profiling and connectivity map analysis
Tác giả: Tianyu Sun, Shalini Singh, Hayson Chenyu Wang, Juseong Lee, Hamid Dolatshad, Pak Leng Cheong, Douglas R Higgs, Jacqueline Boultwood, Andrea Pellagatti
Xuất bản: England: British journal of haematology , 2025
Bộ sưu tập: NCBI
ddc:  355.73
 
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