Biblio

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2024
Sprengel R, Eltokhi A, Single FN. Generation of Rare Human NMDA Receptor Variants in Mice. Methods Mol Biol. 2024;2799:79-105.
Gunawardena N, Chou ST. Generation of red blood cells from induced pluripotent stem cells. Curr Opin Hematol. 2024.
Fitzgerald MQ, Chu T, Puppo F, Blanch R, Chillón M, Subramaniam S, Muotri AR. Generation of 'semi-guided' cortical organoids with complex neural oscillations. Nat Protoc. 2024.
Kindler U, Zaehres H, Mavrommatis L. Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells. Bio Protoc. 2024;14(9):e4984.
Klimpel M, Terrao M, Bräuer M, Dersch H, Biserni M, Nascimento LMelo Do, Schwingal S, Vogel JE, Ferlemann C, Brandt T, et al. Generation of stable suspension producer cell lines for serum-free lentivirus production. Biotechnol J. 2024;19(5):e2400090.
Wang Y-B, Lv Y-F, Zhang Y, Wang W. Generation of the human induced pluripotent stem cell line PUMCi005-A from a patient with Perrault syndrome. Stem Cell Res. 2024;75:103318.
Villegas LDuque, Chandrasekaran A, Andersen SAmalie Fli, Nørremølle A, Schmid B, Pouladi MA, Freude K. Generation of three isogenic gene-edited Huntington's disease human embryonic stem cell lines with DOX-inducible NGN2 expression cassette in the AAVS1 safe locus. Stem Cell Res. 2024;77:103408.
Pierre M, Jauvin D, Puymirat J, Boutjdir M, Chahine M. Generation of three myotonic dystrophy type 1 patient iPSC lines (CBRCULi018-A, CBRCULi019-A, CBRCULi020-A) derived from lymphoblastoid cell lines for disease modelling and therapeutic research. Stem Cell Res. 2024;76:103375.
Mullen MK, Kojic A, Alamana C, Canel G, Lai C, Knowles JW, Wu JC. Generation of two induced pluripotent stem cell lines from healthy patients of African American ancestry. Stem Cell Res. 2024;76:103322.
Edwards S, Hagenau L, Nowack B, Rhode J, Hossain MF, Tzvetkova A, Jensen LR, Kuss AW. Generation of two isogenic iPSC lines from a healthy male donor of European ancestry. Stem Cell Res. 2024;77:103403.
Kamand M, Taleb R, Wathikthinnakon M, Mohamed FAbdullahi, Ghazanfari SPasalar, Konstantinov D, Hald JLaugård, Holst B, Brasch-Andersen C, Møller RS, et al. Generation of two patient specific GABRD variants and their isogenic controls for modeling epilepsy. Stem Cell Res. 2024;76:103372.
Sood A, Mansoor N, Memmi C, Lynch M, Lynch J. Generative pretrained transformer-4, an artificial intelligence text predictive model, has a high capability for passing novel written radiology exam questions. Int J Comput Assist Radiol Surg. 2024.
Guo Y, Xie Y, Qin J. A generic pump-free organ-on-a-chip platform for assessment of intestinal drug absorption. Biotechnol J. 2024;19(2):e2300390.
Lahry K, Datta M, Varshney U. Genetic analysis of translation initiation in bacteria: An initiator tRNA-centric view. Mol Microbiol. 2024.
Koskuvi M, Pörsti E, Hewitt T, Räsänen N, Wu Y-C, Trontti K, McQuade A, Kalyanaraman S, Ojansuu I, Vaurio O, et al. Genetic contribution to microglial activation in schizophrenia. Mol Psychiatry. 2024.
Li Y, Liu B, Chen Y, Liu Z, Ye D, Mao Y, Sun X. Genetic Evidence for the Causal Association of Circulating Cytokines and Growth Factors With Coronary Artery Disease. J Am Heart Assoc. 2024:e030726.
Saha D, Kothari S, Kulkarni SDuttaprasa, Thambiraja M, Yennamalli RM, Das DK. Genetic heterogeneity and respiratory chain enzyme analysis in pediatric Indian patients with mitochondrial disorder: Report of novel variants in POLG1 gene and their functional implication using molecular dynamic simulation. Mitochondrion. 2024:101870.
Chen Y, Li X, Lu R, Lv Y, Ye J, Huang Q, Meng W, Long F, Burman J, Mo XM, et al. Genetic insights into across pancreatitis types: the causal influence of immunoglobulin G N-glycosylation variants on disease risk. Front Immunol. 2024;15:1326370.
Baranwal A, Gurney M, Basmaci R, Katamesh B, He R, Viswanatha DS, Greipp P, Foran J, Badar T, Murthy H, et al. Genetic landscape and clinical outcomes of patients with BCOR mutated myeloid neoplasms. Haematologica. 2024.
Cheung S, Ng L, Xie P, Kocur O, Elias R, Schlegel P, Rosenwaks Z, Palermo GD. Genetic profiling of azoospermic men to identify the etiology and predict reproductive potential. J Assist Reprod Genet. 2024.
LeBleu VS, Kanasaki K, Lovisa S, Alge JL, Kim J, Chen Y, Teng Y, Gerami-Naini B, Sugimoto H, Kato N, et al. Genetic reprogramming with stem cells regenerates glomerular epithelial podocytes in Alport syndrome. Life Sci Alliance. 2024;7(6).
Wu H, Lv P, Wang J, Bennett B, Wang J, Li P, Peng Y, Hu G, Lin J. Genetic screen identified PRMT5 as a neuroprotection target against cerebral ischemia. Elife. 2024;12.
Nie S, Zhang W, Jin X, Li X, Sun S, Zhao Y, Jia Q, Li L, Liu Y, Liu D, et al. Genetic Screening of Haploid Neural Stem Cells Reveals that Nfkbia and Atp2b4 are Key Regulators of Oxidative Stress in Neural Precursors. Adv Sci (Weinh). 2024:e2309292.
Hu J, Korchina V, Zouk H, Harden MV, Murdock D, Macbeth A, Harrison SM, Lennon N, Kovar C, Balasubramanian A, et al. Genetic sex validation for sample tracking in next-generation sequencing clinical testing. BMC Res Notes. 2024;17(1):62.
Nathans JF, Ayers JL, Shendure J, Simpson CL. Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin. J Invest Dermatol. 2024;144(5):936-949.

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