Results 81 to 90 of about 2,618 (150)

Supplementary Figure S7 from Predictive Biomarkers for Adjuvant Capecitabine Benefit in Early-Stage Triple-Negative Breast Cancer in the FinXX Clinical Trial

, 2020
Supplementary Figure S7 shows scatter plots for TYMP expression against selected genes and ...
Amy Sullivan (4614715), Karama Asleh (15030080), E. Aubrey Thompson (13037596), Heather Ann Brauer (14991284), Torsten O. Nielsen (8306832), Heikki Joensuu (15012681), Saranya Chumsri (38251), Susanna Lauttia (3564638), Henrik Lindman (369388)   +8 more
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Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far

Frontiers in Genetics, 2018
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an ultra-rare metabolic autosomal recessive disease, caused by mutations in the nuclear gene TYMP which encodes the enzyme thymidine phosphorylase.
Dario Pacitti, Michelle Levene, Caterina Garone, Niranjanan Nirmalananthan, Bridget E. Bax   +4 more
doaj   +1 more source

Additional file 2: of The impact of environmental factors in pre-hospital thermistor-based tympanic temperature measurement: a pilot field study

, 2016
Concordance correlation coefficients for Δ Trect-tymp.
Jörg Aßmus (199507), Guttorm Brattebø (3574664), Øyvind Thomassen (3574667), Sven Skaiaa (3574661)   +3 more
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Дифференциальная диагностика митохондриальной нейрогастроинтестинальной энцефаломиопатии. Первое клиническое описание в России [PDF]

, 2015
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) is a rare autosomal recessive progressive multisystem disorder. Most of MNGIE is caused by mutations in the gene encoding thymidine phosphorylase (TYMP), locus 22q13.
S. N. Lipovka, P. G. Tsygankova, С. Н. Липовка, S. A. Kurbatov, П. Г. Цыганкова, E. Y. Zakharova, В. П. Федотов, V. P. Fedotov, С. А. Курбатов, Е. Ю. Захарова   +9 more
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Proteomic profiling of gliomas unveils immune and metabolism-driven subtypes with implications for anti-nucleotide metabolism therapy

Nature Communications
Gliomas exhibit high heterogeneity and poor prognosis. Despite substantial progress has been made at the genomic and transcriptomic levels, comprehensive proteomic characterization and its implications remain largely unexplored. In this study, we perform
Jinsen Zhang, Rui Sun, Yingying Lyu, Chaxian Liu, Ying Liu, Yuan Feng, Minjie Fu, Peter Jih Cheng Wong, Zunguo Du, Tianming Qiu, Yi Zhang, Dongxiao Zhuang, Zhiyong Qin, Yu Yao, Wei Zhu, Tiannan Guo, Wei Hua, Hui Yang, Ying Mao   +18 more
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Meningoencephalitis in a novel mutation in MNGIE (mitochondrial neurogastrointestinal encephalomyopathy) ending a familial diagnostic odyssey: A case series report

Journal of Central Nervous System Disease
MNGIE (Mitochondrial Neurogastrointestinal Encephalomyopathy) is an ultra-rare autosomal recessive disorder that leads to mutations in the nuclear genes encoding thymidine phosphorylase.
Noor Redha, Zahra Al-Sahlawi, Hasan Hasan, Sara Ghareeb, Hani Humaidan   +4 more
doaj   +1 more source

Integrated Multi-Omics Analyses Identify TYMP as a Candidate Protective Immunoregulatory Marker in CD4⁺ T Cells During Sepsis

Journal of Inflammation Research
Yanan Wang,1,2,* Jianglin Zhao,1,2,* Yushi Zhang,1,* Ji Shen,1 Yuan Shi,1 Qingxiang Liu,3 Xuefeng Zhang11Department of Critical Care Medicine, The Affiliated Jiangyin Hospital of Nantong University, Wuxi, 214400, People’s Republic
Wang Y, Zhao J, Zhang Y, Shen J, Shi Y, Liu Q, Zhang X   +6 more
doaj  

Mitochondrial Neurogastrointestinal Encephalomyopathy: Novel Pathogenic Mutations in Thymidine Phosphorylase Gene in Two Italian Brothers

, 2012
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE, MIM 603041) is an autosomal recessive multisystem disorder occurring due to mutations in a nuclear gene coding for the enzyme thymidine phosphorylase (TYMP). Clinical features of MNGIE include
LUPIS, CHIARA, INGHILLERI, Maurizio, LIBERNINI, LAURA, Filippo Santorelli, LEUZZI, Vincenzo, MASTRANGELO, Mario, Rosalba Carrozzo   +6 more
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Mitochondrial Neurogastrointestinal Encephalomyopathy: Novel Pathogenic Mutation in Thymidine Phosphorylase Gene in a Patient from Cape Verde Islands

Case Reports in Neurological Medicine, 2019
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE) is a rare autosomal recessive disorder caused by mutations in the gene encoding the Thymidine Phosphorylase (TP).
Catarina Falcão de Campos, Miguel Oliveira Santos, Rafael Roque, Isabel Conceição, Mamede de Carvalho   +4 more
doaj   +1 more source

Valtavirtapolitiikan murros USA:n presidentinvaaleissa

, 2022
Äänestäjien tympääntyminen USA:n valtavirtapolitiikkaan ja populismin nousu.
Heiskanen Benita
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