lactic acid has been researched along with Genetic Predisposition in 22 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
Excerpt | Relevance | Reference |
---|---|---|
"Genetic factors play a role in the development of lactic acidosis after OLT." | 7.78 | The association of promoter gene polymorphisms of the tumor necrosis factor-α and interleukin-10 with severity of lactic acidosis during liver transplantation surgery. ( Abouelfetoh, F; Baz, H; Farahat, O; Labib, D; Mokhtar, A; Salah, M, 2012) |
"Genetic factors play a role in the development of lactic acidosis after OLT." | 3.78 | The association of promoter gene polymorphisms of the tumor necrosis factor-α and interleukin-10 with severity of lactic acidosis during liver transplantation surgery. ( Abouelfetoh, F; Baz, H; Farahat, O; Labib, D; Mokhtar, A; Salah, M, 2012) |
"Clear cell renal cell carcinoma (ccRCC) is the most common pathological subtype of kidney cancer." | 2.48 | Genome-wide RNA interference analysis of renal carcinoma survival regulators identifies MCT4 as a Warburg effect metabolic target. ( Burrell, RA; Dykema, K; Endesfelder, D; Gerlinger, M; Howell, M; Jiang, M; Kelly, G; Larkin, J; Martinez, P; Patard, JJ; Rioux-Leclercq, N; Santos, CR; Saunders, RE; Spencer-Dene, B; Stamp, G; Swanton, C; Vetter, M, 2012) |
"Specific treatment of mitochondrial diseases is in its infancy and is a major challenge for pediatric medicine." | 2.44 | Disorders of mitochondrial function. ( Debray, FG; Lambert, M; Mitchell, GA, 2008) |
"The pathophysiology of febrile seizures remains unclear." | 1.48 | Interleukin-4 and tumor necrosis factor-alpha levels in children with febrile seizures. ( Bae, SH; Choi, J; Ha, J; Kim, K; Kim, SJ; Kim, SN; Kwak, BO; Kwon, A; Lee, R; Son, JS, 2018) |
"PDHc deficiency was demonstrated in muscle and fibroblasts without detectable PDHA1 mutations." | 1.36 | Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain. ( Briones, P; Font, A; Pineda, M; Quintana, E; Ribes, A; Tort, F; Vilaseca, MA, 2010) |
"Lactic acid levels were documented at five different time points: 10 min after beginning of cardiopulmonary bypass, 40 min after cardiopulmonary bypass termination, and 30 min, 8h, and 16 h after the surgery." | 1.33 | IL-10 and TNF-beta gene polymorphisms have no major influence on lactate levels after cardiac surgery. ( Brezina, A; Hubacek, JA; Kellovsky, P; Pirk, J; Poledne, R; Riha, H, 2006) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (13.64) | 18.2507 |
2000's | 5 (22.73) | 29.6817 |
2010's | 12 (54.55) | 24.3611 |
2020's | 2 (9.09) | 2.80 |
Authors | Studies |
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Yuan, Y | 1 |
Sun, L | 2 |
Wang, X | 2 |
Chen, J | 1 |
Jia, M | 1 |
Zou, Y | 1 |
Sa, H | 1 |
Cai, Y | 1 |
Xu, Y | 2 |
Sun, C | 1 |
Guo, Y | 1 |
Li, H | 1 |
Ma, K | 1 |
Ye, Z | 1 |
Wu, C | 1 |
Zhang, N | 1 |
Du, L | 1 |
Cao, Q | 1 |
Huang, X | 1 |
Tang, J | 1 |
Wang, Q | 1 |
Li, F | 1 |
Zhou, C | 1 |
Xu, Q | 1 |
Xiong, X | 1 |
Kijlstra, A | 1 |
Qin, N | 1 |
Yang, P | 1 |
Gupta, JK | 1 |
Care, A | 1 |
Goodfellow, L | 1 |
Alfirevic, Z | 1 |
Lian, LY | 1 |
Müller-Myhsok, B | 1 |
Alfirevic, A | 1 |
Phelan, MM | 1 |
Wei, YL | 1 |
Tian, Q | 1 |
Zhao, XX | 1 |
Qiu, GZ | 1 |
Ha, J | 1 |
Choi, J | 1 |
Kwon, A | 1 |
Kim, K | 1 |
Kim, SJ | 1 |
Bae, SH | 1 |
Son, JS | 1 |
Kim, SN | 1 |
Kwak, BO | 1 |
Lee, R | 1 |
Pacheu-Grau, D | 1 |
Callegari, S | 1 |
Emperador, S | 1 |
Thompson, K | 1 |
Aich, A | 1 |
Topol, SE | 1 |
Spencer, EG | 1 |
McFarland, R | 1 |
Ruiz-Pesini, E | 1 |
Torkamani, A | 1 |
Taylor, RW | 1 |
Montoya, J | 1 |
Rehling, P | 1 |
Zhang, Y | 1 |
Wang, T | 1 |
Li, X | 1 |
Ma, Y | 1 |
Akasaka, T | 1 |
Hokimoto, S | 1 |
Sueta, D | 1 |
Tabata, N | 1 |
Sakamoto, K | 1 |
Yamamoto, E | 1 |
Yamamuro, M | 1 |
Tsujita, K | 1 |
Kojima, S | 1 |
Kaikita, K | 1 |
Kajiwara, A | 1 |
Morita, K | 1 |
Oniki, K | 1 |
Saruwatari, J | 1 |
Nakagawa, K | 1 |
Ogata, Y | 1 |
Ogawa, H | 1 |
Cordani, M | 1 |
Pacchiana, R | 1 |
Butera, G | 1 |
D'Orazi, G | 1 |
Scarpa, A | 1 |
Donadelli, M | 1 |
Dewulf, JP | 1 |
Barrea, C | 1 |
Vincent, MF | 1 |
De Laet, C | 1 |
Van Coster, R | 1 |
Seneca, S | 1 |
Marie, S | 1 |
Nassogne, MC | 1 |
Debray, FG | 1 |
Lambert, M | 1 |
Mitchell, GA | 1 |
Dela, F | 1 |
Stallknecht, B | 1 |
Quintana, E | 1 |
Pineda, M | 1 |
Font, A | 1 |
Vilaseca, MA | 1 |
Tort, F | 1 |
Ribes, A | 1 |
Briones, P | 1 |
Gerlinger, M | 1 |
Santos, CR | 1 |
Spencer-Dene, B | 1 |
Martinez, P | 1 |
Endesfelder, D | 1 |
Burrell, RA | 1 |
Vetter, M | 1 |
Jiang, M | 1 |
Saunders, RE | 1 |
Kelly, G | 1 |
Dykema, K | 1 |
Rioux-Leclercq, N | 1 |
Stamp, G | 1 |
Patard, JJ | 1 |
Larkin, J | 1 |
Howell, M | 1 |
Swanton, C | 1 |
Farahat, O | 1 |
Salah, M | 1 |
Mokhtar, A | 1 |
Abouelfetoh, F | 1 |
Labib, D | 1 |
Baz, H | 1 |
Hassanzadeh, M | 1 |
Gilanpour, H | 1 |
Charkhkar, S | 1 |
Buyse, J | 1 |
Decuypere, E | 1 |
Riha, H | 1 |
Hubacek, JA | 1 |
Poledne, R | 1 |
Kellovsky, P | 1 |
Brezina, A | 1 |
Pirk, J | 1 |
Sperl, W | 1 |
Jesina, P | 1 |
Zeman, J | 1 |
Mayr, JA | 1 |
Demeirleir, L | 1 |
VanCoster, R | 1 |
Pícková, A | 1 |
Hansíková, H | 1 |
Houst'ková, H | 1 |
Krejcík, Z | 1 |
Koch, J | 1 |
Smet, J | 1 |
Muss, W | 1 |
Holme, E | 1 |
Houstek, J | 1 |
Beauchamp, NJ | 1 |
Taybert, J | 1 |
Champion, MP | 1 |
Layet, V | 1 |
Heinz-Erian, P | 1 |
Dalton, A | 1 |
Tanner, MS | 1 |
Pronicka, E | 1 |
Sharrard, MJ | 1 |
Lockette, W | 1 |
Kirkland, K | 1 |
Farrow, S | 1 |
Griez, E | 1 |
Schruers, K | 1 |
Balasubramanyam, A | 1 |
McKay, S | 1 |
Nadkarni, P | 1 |
Rajan, AS | 1 |
Garza, A | 1 |
Pavlik, V | 1 |
Herd, JA | 1 |
Jahoor, F | 1 |
Reeds, PJ | 1 |
4 reviews available for lactic acid and Genetic Predisposition
Article | Year |
---|---|
Mutant p53 proteins alter cancer cell secretome and tumour microenvironment: Involvement in cancer invasion and metastasis.
Topics: Animals; Cell Communication; Cell Movement; Cytokines; Extracellular Matrix; Genetic Predisposition | 2016 |
Disorders of mitochondrial function.
Topics: Child; Citric Acid Cycle; DNA, Mitochondrial; Genetic Predisposition to Disease; Humans; Lactic Acid | 2008 |
Genome-wide RNA interference analysis of renal carcinoma survival regulators identifies MCT4 as a Warburg effect metabolic target.
Topics: Apoptosis; Carcinoma, Renal Cell; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Cell | 2012 |
Experimental pathophysiology of panic.
Topics: Carbon Dioxide; Female; Genetic Predisposition to Disease; Humans; Lactic Acid; Male; Models, Biolog | 1998 |
18 other studies available for lactic acid and Genetic Predisposition
Article | Year |
---|---|
Identification of a new
Topics: Alternative Splicing; Animals; Base Sequence; Cell Cycle Proteins; Cell Line, Tumor; Cell Proliferat | 2019 |
Altered gut microbiome composition in patients with Vogt-Koyanagi-Harada disease.
Topics: Adrenal Cortex Hormones; Adult; Animals; Biodiversity; Butyrates; Disease Models, Animal; DNA, Bacte | 2020 |
Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach.
Topics: Adult; Biomarkers; Case-Control Studies; Female; Genetic Predisposition to Disease; Genome-Wide Asso | 2021 |
Association between MFN2 gene polymorphisms and the risk and prognosis of acute liver failure: a case-control study in a Chinese population.
Topics: Adult; Ammonia; Asian People; Case-Control Studies; China; Female; Gene Frequency; Genetic Predispos | 2017 |
Interleukin-4 and tumor necrosis factor-alpha levels in children with febrile seizures.
Topics: Biomarkers; Child; Child, Preschool; Female; Genetic Predisposition to Disease; Humans; Interleukin- | 2018 |
Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy.
Topics: Carrier Proteins; Child; DNA, Mitochondrial; Exome Sequencing; Female; Fibroblasts; Genetic Predispo | 2018 |
The evaluation of neural and vascular hyper-reactivity for sensitive skin.
Topics: Adolescent; Adult; Capsaicin; Female; Genetic Predisposition to Disease; Humans; Hyperalgesia; Lacti | 2016 |
Sex differences in the impact of CYP2C19 polymorphisms and low-grade inflammation on coronary microvascular disorder.
Topics: Aged; Biomarkers; C-Reactive Protein; Case-Control Studies; Chi-Square Distribution; Coronary Artery | 2016 |
Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patients.
Topics: Acyl-CoA Dehydrogenases; Adult; Child; Female; Genetic Predisposition to Disease; Heart Diseases; Hu | 2016 |
Effect of physical training on insulin secretion and action in skeletal muscle and adipose tissue of first-degree relatives of type 2 diabetic patients.
Topics: Adipose Tissue; Adult; Blood Glucose; Body Composition; C-Peptide; Diabetes Mellitus, Type 2; Exerci | 2010 |
Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain.
Topics: Acidosis, Lactic; Adult; Amino Acid Sequence; Base Sequence; Biomarkers; Blepharoptosis; Cells, Cult | 2010 |
The association of promoter gene polymorphisms of the tumor necrosis factor-α and interleukin-10 with severity of lactic acidosis during liver transplantation surgery.
Topics: Acidosis, Lactic; Adult; Biomarkers; Egypt; Female; Genetic Predisposition to Disease; Heterozygote; | 2012 |
Anatomical parameters of cardiopulmonary system in three different lines of chickens: further evidence for involvement in ascites syndrome.
Topics: Aging; Animals; Ascites; Body Weight; Cardiovascular System; Chickens; Genetic Predisposition to Dis | 2005 |
IL-10 and TNF-beta gene polymorphisms have no major influence on lactate levels after cardiac surgery.
Topics: Adult; Aged; Biomarkers; Coronary Artery Bypass; Female; Gene Frequency; Genetic Predisposition to D | 2006 |
Deficiency of mitochondrial ATP synthase of nuclear genetic origin.
Topics: Adenosine Triphosphate; Adolescent; Age of Onset; Cardiomyopathy, Hypertrophic, Familial; Cell Nucle | 2006 |
High frequency of missense mutations in glycogen storage disease type VI.
Topics: Amino Acid Sequence; Animals; Blood Glucose; Child, Preschool; DNA Mutational Analysis; Exons; Femal | 2007 |
Alpha 2-adrenergic agonists increase cellular lactate efflux.
Topics: Adrenergic alpha-Agonists; Animals; Body Temperature Regulation; Cells, Cultured; Cerebrovascular Di | 1996 |
Ethnicity affects the postprandial regulation of glycogenolysis.
Topics: Adult; Asian People; Blood Glucose; Carbon Isotopes; Diabetes Mellitus, Type 2; Energy Metabolism; G | 1999 |