Biblio

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Sharma N, Gupta M, Nabi G, Biswas S, Ali S, Sarwat M. Variation in the anti-oxidant, anti-obesity, and anti-cancer potential of different polarity extracts of saffron petals. 3 Biotech. 2023;13(7):249.
Young KA, Telpoukhovskaia MA, Hofmann J, Mistry JJ, Kokkaliaris K, Trowbridge JJ. Variation in Mesenchymal KITL/SCF and IGF1 Expression at Middle Age Underlies Steady-State Hematopoietic Stem Cell Aging. Blood. 2024.
Kortleve JP, Kisch AM, Piepenbroek B, Mooyaart JE, Kozijn AE, Sohne M, Liptrott SJ. Variation in hydration use after reinfusion of autologous stem cells in dimethyl sulfoxide (DMSO): a survey of EBMTcenters on behalf of the EBMT Nurses Group. Bone Marrow Transplant. 2023.
Kumar V, Pouw RB, Autio MI, Sagmeister MG, Phua ZYang, Borghini L, Wright VJ, Hoggart C, Pan B, Tan AKiat Yee, et al. Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations. Am J Hum Genet. 2022.
Ranjbari AGhorbani, Mehrzad J, Dehghani H, Abdollahi A, Hosseinkhani S. Variation in Blood and Colorectal Epithelia's Key Trace Elements Along with Expression of Mismatch Repair Proteins from Localized and Metastatic Colorectal Cancer Patients. Biol Trace Elem Res. 2019.
Littleton SH, Trang KB, Volpe CM, Cook K, DeBruyne N, Maguire JAnn, Weidekamp MAnn, Hodge KM, Boehm K, Lu S, et al. Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2. Cell Genom. 2024:100556.
Peng L, Renauer PA, Ökten A, Fang Z, Park JJ, Zhou X, Lin Q, Dong MB, Filler R, Xiong Q, et al. Variant-specific vaccination induces systems immune responses and potent in vivo protection against SARS-CoV-2. Cell Rep Med. 2022:100634.
Onal G, Yalçın-Çakmaklı G, Özçelik CE, Boussaad I, Şeker UÖŞ, Fernandes HJR, Demir H, Krüger R, Elibol B, Dökmeci S, et al. Variant-specific effects of GBA1 mutations on dopaminergic neuron proteostasis. J Neurochem. 2024.
Nam DEun, Park JHee, Park CEun, Jung NYoung, Nam SHyun, Kwon HMi, Kim HSu, Kim SBeom, Son WSeok, Choi B-O, et al. Variants of aminoacyl-tRNA synthetase genes in Charcot-Marie-Tooth disease: a Korean cohort study. J Peripher Nerv Syst. 2021.
Wallgren-Pettersson C, Jokela M, Lehtokari V-L, Tyynismaa H, Sainio MT, Ylikallio E, Tynninen O, Pelin K, Auranen M. Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia. Neuromuscul Disord. 2023;35:29-32.
Trevisan CMartins, Naslavsky MSatya, Monfardini F, Wang J, Zatz M, Peluso C, Pellegrino R, Mafra F, Hakonarson H, Ferreira FMoraes, et al. Variants in the Kisspeptin-GnRH Pathway Modulate the Hormonal Profile and Reproductive Outcomes. DNA Cell Biol. 2020.
Sanjurjo-Soriano C, Jimenez-Medina C, Erkilic N, Cappellino L, Lefevre A, Nagel-Wolfrum K, Wolfrum U, Van Wijk E, Roux A-F, Meunier I, et al. variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids. HGG Adv. 2023;4(4):100229.
Pahl MC, Liu L, Pippin JA, Wagley Y, Boehm K, Hankenson KD, Wells AD, Yang W, Grant SFA. Variant to gene mapping for carpal tunnel syndrome risk loci implicates skeletal muscle regulatory elements. EBioMedicine. 2024;101:105038.
Bernardi S, Bonifacio M, Iurlo A, Zanaglio C, Tiribelli M, Binotto G, Abruzzese E, Russo D. "Variant specific discrepancy when quantitating BCR-ABL1 e13a2 and e14a2 transcripts using the Europe Against Cancer qPCR assay". Is dPCR the key?. Eur J Haematol. 2019.
Kjaer L, Skov V, Andersen MTolstrup, Aggerholm A, Clair P, Gniot M, Soeby K, Udby L, Dorff MHelleberg, Hasselbalch H, et al. Variant specific discrepancy when quantitating BCR-ABL1 e13a2 and e14a2 transcripts using the Europe Against Cancer qPCR assay. Eur J Haematol. 2019.
Schulz M, Karpova D, Spohn G, Damert A, Seifried E, Binder V, Bonig H. Variant rs1801157 in the 3'UTR of SDF-1ß Does Not Explain Variability of Healthy-Donor G-CSF Responsiveness. PLoS One. 2015;10(3):e0121859.
Phan CLee, Tan SNgoh, Tan SMui, Kadir SShahnaz Sy, Ramli NLiyana Moh, Lim TOnn, Ng CChing. A variant e13a3 BCR-ABL1 fusion transcript in refractory adult B-cell acute lymphoblastic leukemia achieving complete remission with CAR-Tcell therapy. Cancer Genet. 2020;250-251:20-24.
Wu CY, Yang SW, Li YL, Dong XY, Yu RH, Zhang L, Shang BJ, Shi PL, Zhu ZM. [Variant acute promyelocytic leukemia with IRF2BP2-RARA fusion gene: a case report and literature review]. Zhonghua Xue Ye Xue Za Zhi. 2023;44(3):251-254.
Chiesa R, Boelens JJan, Duncan CN, Kuehl J-S, Sevin C, Kapoor N, Prasad VK, Lindemans CA, Jones SA, Amartino HM, et al. Variables Affecting Outcomes After Allogeneic Hematopoietic Stem Cell Transplant for Cerebral Adrenoleukodystrophy. Blood Adv. 2021.
Doi Y, Yokota T, Satoh Y, Okuzaki D, Tokunaga M, Ishibashi T, Sudo T, Ueda T, Shingai Y, Ichii M, et al. Variable SATB1 Levels Regulate Hematopoietic Stem Cell Heterogeneity with Distinct Lineage Fate. Cell Rep. 2018;23(11):3223-3235.
Ingwersen V, Hofmann J, Muche M, le Coutre P, Schneider T, Leng C, Burmeister T, Maschmeyer G, Keller U, Schwartz S. Variable outcomes of hepatitis E infections in patients with hemato-oncologic diseases. Oncol Res Treat. 2023.
Strano A, Tuck E, Stubbs VE, Livesey FJ. Variable Outcomes in Neural Differentiation of Human PSCs Arise from Intrinsic Differences in Developmental Signaling Pathways. Cell Rep. 2020;31(10):107732.
Jin Y-Y, Zhou W, Tian Z-Q, Chen T-X. Variable clinical phenotypes of X-Linked lymphoproliferative syndrome in China: Report of five cases with three novel mutations and review of the literature. Hum Immunol. 2016.
Chen X, Vinokurov AY, Zherebtsov EA, Stelmashchuk OA, Angelova PR, Esteras N, Abramov AY. Variability of mitochondrial energy balance across brain regions. J Neurochem. 2020.
Kamel AM, El-Fishawi S, Rasekh EO, Radwan ER, Zeidan A, El-Said A, Zaky AH, Abdelfattah M, Refaat A, Abdelfattah R. Variability of contribution of vitamin D receptor gene polymorphisms to outcome of HLA-matched sibling allogeneic bone marrow transplantation. Leuk Lymphoma. 2018:1-10.

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