Biblio

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

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Frede N, Rojas-Restrepo J, de Oteyza ACaballero, Buchta M, Hübscher K, Gámez-Díaz L, Proietti M, Saghafi S, Chavoshzadeh Z, Soler-Palacín P, et al. Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis. J Clin Immunol. 2021.

Song N, Wang Y, Zhou L, Zhang J, Wu F, Li M, Wang W, Liu Y, Lu X, Chen Q, et al. Genetic analysis of the LRP10 gene in Chinese patients with Parkinson's disease. Neurol Sci. 2022.

Al-Jamea L'aH, Woodman A, Heiba NMohamed, Elshazly SA, Ben Khalaf N, Fathallah DM, Al-Nashmi ME, Quiambao JVecina, Deifalla AHalim. Genetic analysis of TMPRSS6 gene in Saudi female patients with iron deficiency anemia. Hematol Oncol Stem Cell Ther. 2020.

Lahry K, Datta M, Varshney U. Genetic analysis of translation initiation in bacteria: An initiator tRNA-centric view. Mol Microbiol. 2024.

Zhao C, Zhang Q, Zhang R, Lian H, Ma H, Zhao X, Li Z. Genetic and clinical characteristics of primary hemophagocytic lymphohistiocytosis in children. Ann Hematol. 2023.

Agarwal A, Cooke L, Riley C, Qi W, Mount D, Mahadevan D. Genetic and cytokine changes associated with symptomatic stages of CLL. Leuk Res. 2014.

Do DVinh, Ueda J, Messerschmidt DM, Lorthongpanich C, Zhou Y, Feng B, Guo G, Lin PJ, Hossain MZakir, Zhang W, et al. A genetic and developmental pathway from STAT3 to the OCT4-NANOG circuit is essential for maintenance of ICM lineages in vivo. Genes Dev. 2013;27(12):1378-1390.

Upadhyaya P, Di Serafino A, Sorino L, Ballerini P, Marchisio M, Pierdomenico L, Stuppia L, Antonucci I. Genetic and epigenetic modifications induced by chemotherapeutic drugs: human amniotic fluid stem cells as an in-vitro model. BMC Med Genomics. 2019;12(1):146.

Sharma S, Bhonde R. Genetic and epigenetic stability of stem cells: Epigenetic modifiers modulate the fate of mesenchymal stem cells. Genomics. 2020.

Eadon MT, Wheeler HE, Stark AL, Zhang X, Moen EL, Delaney SM, Im HKyung, Cunningham PN, Zhang W, M Dolan E. Genetic and epigenetic variants contributing to clofarabine cytotoxicity. Hum Mol Genet. 2013.

Kim K-H, Hong EPyo, Shin JWan, Chao MJ, Loupe J, Gillis T, Mysore JS, Holmans P, Jones L, Orth M, et al. Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects. Am J Hum Genet. 2020.

Shinoda K, Luijten IHN, Hasegawa Y, Hong H, Sonne SB, Kim M, Xue R, Chondronikola M, Cypess AM, Tseng Y-H, et al. Genetic and functional characterization of clonally derived adult human brown adipocytes. Nat Med. 2015.

Jhamb S, Vangaveti VN, Malabu UH. Genetic and molecular basis of diabetic foot ulcers: Clinical review. J Tissue Viability. 2016.

Sexton AN, Regalado SG, Lai CS, Cost GJ, O'Neil CM, Urnov FD, Gregory PD, Jaenisch R, Collins K, Hockemeyer D. Genetic and molecular identification of three human TPP1 functions in telomerase action: recruitment, activation, and homeostasis set point regulation. Genes Dev. 2014.

Lintott LG, Nutter LMJ. Genetic and Molecular Quality Control of Genetically Engineered Mice. Methods Mol Biol. 2023;2631:53-101.

Turner REmily, Harrison PF, Swaminathan A, Kraupner-Taylor CA, Goldie BJ, See M, Peterson AL, Schittenhelm RB, Powell DR, Creek DJ, et al. Genetic and pharmacological evidence for kinetic competition between alternative poly(A) sites in yeast. Elife. 2021;10.

Portal B, Delcourte S, Rovera R, Lejards C, Bullich S, Malnou CE, Haddjeri N, Déglon N, Guiard BP. Genetic and pharmacological inactivation of astroglial connexin 43 differentially influences the acute response of antidepressant and anxiolytic drugs. Acta Physiol (Oxf). 2020.

Monfared MM, Dao TQ, Fletcher JC. Genetic and Phenotypic Analysis of Shoot Apical and Floral Meristem Development. Methods Mol Biol. 2023;2686:163-198.

Peng L, Dreumont N, Coelho D, Guéant J-L, Arnold C. Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency. Biochimie. 2016.

Natri HM, Hudjashov G, Jacobs G, Kusuma P, Saag L, Darusallam CCrenna, Metspalu M, Sudoyo H, Cox MP, Romero IGallego, et al. Genetic architecture of gene regulation in Indonesian populations identifies QTLs associated with global and local ancestries. Am J Hum Genet. 2021.

Fair T, Pollen AA. Genetic architecture of human brain evolution. Curr Opin Neurobiol. 2023;80:102710.

Sha Z, Schijven D, Fisher SE, Francks C. Genetic architecture of the white matter connectome of the human brain. Sci Adv. 2023;9(7):eadd2870.

Min Y, Ballerini ES, Edwards MB, Hodges SA, Kramer EM. Genetic architecture underlying variation in floral meristem termination in Aquilegia. J Exp Bot. 2022.

Wu W, Li C, Zhu X, Liu X, Li P, Wan R, Wu X, Chen S. Genetic association of telomere length, obesity and tobacoo smoking with idiopathic pulmonary fibrosis risk. BMC Public Health. 2023;23(1):868.

Luo J, Thomassen JQvist, Bellenguez C, Grenier-Boley B, de Rojas I, Castillo A, Parveen K, Küçükali F, Nicolas A, Peters O, et al. Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease. JAMA Netw Open. 2023;6(5):e2313734.

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