carnitine has been researched along with Abnormalities, Autosome in 11 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "In this study, the modulating effect of L-carnitine on tert-butyl-hydroperoxide-induced DNA damage was compared with that of mannitol, a well known scavenger of hydroxyl radicals, both in normal and Ataxia telangiectasia mutated (ATM)-deficient lymphoblastoid cell lines established from A." | 7.74 | L-carnitine enhances resistance to oxidative stress by reducing DNA damage in Ataxia telangiectasia cells. ( Berni, A; Chessa, L; De Amicis, A; Filippi, S; Meschini, R; Palitti, F, 2008) |
| "In this study, the modulating effect of L-carnitine on tert-butyl-hydroperoxide-induced DNA damage was compared with that of mannitol, a well known scavenger of hydroxyl radicals, both in normal and Ataxia telangiectasia mutated (ATM)-deficient lymphoblastoid cell lines established from A." | 3.74 | L-carnitine enhances resistance to oxidative stress by reducing DNA damage in Ataxia telangiectasia cells. ( Berni, A; Chessa, L; De Amicis, A; Filippi, S; Meschini, R; Palitti, F, 2008) |
| "L-carnitine is a small essential molecule indispensable in fatty acid metabolism and required in several biological pathways regulating cellular homeostasis." | 1.33 | L-Carnitine protects mammalian cells from chromosome aberrations but not from inhibition of cell proliferation induced by hydrogen peroxide. ( Barbieri, R; Lioi, MB; Monfregola, J; Salzano, S; Santoro, A; Ursini, MV, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (9.09) | 18.7374 |
| 1990's | 1 (9.09) | 18.2507 |
| 2000's | 5 (45.45) | 29.6817 |
| 2010's | 3 (27.27) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Bogusiewicz, J | 1 |
| Burlikowska, K | 1 |
| Jaroch, K | 1 |
| Gorynska, PZ | 1 |
| Gorynski, K | 1 |
| Birski, M | 1 |
| Furtak, J | 1 |
| Paczkowski, D | 1 |
| Harat, M | 1 |
| Bojko, B | 1 |
| Pierron, S | 1 |
| Giudicelli, H | 1 |
| Moreigne, M | 1 |
| Khalfi, A | 1 |
| Touati, G | 1 |
| Caruba, C | 1 |
| Rolland, MO | 1 |
| Acquaviva, C | 1 |
| Prada, CE | 1 |
| Jefferies, JL | 1 |
| Grenier, MA | 1 |
| Huth, CM | 1 |
| Page, KI | 1 |
| Spicer, RL | 1 |
| Towbin, JA | 1 |
| Leslie, ND | 1 |
| Ohtaki, U | 1 |
| Ozawa, H | 1 |
| Ishizuka, T | 1 |
| Kamiishi, A | 1 |
| Sasaki, K | 1 |
| Nakajima, S | 1 |
| Katayama, A | 1 |
| Arimoto, K | 1 |
| Yagihashi, T | 1 |
| Kimiya, S | 1 |
| Kinali, M | 1 |
| Olpin, SE | 1 |
| Clayton, PT | 1 |
| Daubeney, PE | 1 |
| Mercuri, E | 1 |
| Manzur, AY | 1 |
| Tein, I | 1 |
| Leonard, J | 1 |
| Muntoni, F | 1 |
| Gordon, N | 1 |
| Santoro, A | 1 |
| Lioi, MB | 1 |
| Monfregola, J | 1 |
| Salzano, S | 1 |
| Barbieri, R | 1 |
| Ursini, MV | 1 |
| Garcia, CL | 1 |
| Filippi, S | 2 |
| Mosesso, P | 1 |
| Calvani, M | 1 |
| Nicolai, R | 1 |
| Mosconi, L | 1 |
| Palitti, F | 2 |
| Berni, A | 1 |
| Meschini, R | 1 |
| De Amicis, A | 1 |
| Chessa, L | 1 |
| Gellera, C | 1 |
| Uziel, G | 1 |
| Rimoldi, M | 1 |
| Zeviani, M | 1 |
| Laverda, A | 1 |
| Carrara, F | 1 |
| DiDonato, S | 1 |
| Shahar, E | 1 |
| Brand, N | 1 |
| Shapira, Y | 1 |
| Barash, V | 1 |
| Gutman, A | 1 |
11 other studies available for carnitine and Abnormalities, Autosome
| Article | Year |
|---|---|
Profiling of Carnitine Shuttle System Intermediates in Gliomas Using Solid-Phase Microextraction (SPME).
Topics: Adult; Aged; Biomarkers, Tumor; Carnitine; Chromosome Aberrations; Female; Glioma; Humans; Isocitrat | 2021 |
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder].
Topics: Alleles; Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Chromosome Aberrations; | 2010 |
Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy.
Topics: Alleles; Carboxy-Lyases; Cardiomyopathies; Carnitine; Chromosome Aberrations; Chromosome Deletion; C | 2012 |
[Evaluation of serum total carnitine values in persons with severe motor and intellectual disabilities with enteral (tube) feeding].
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Carnitine; Cerebral Palsy; Chromosome Aberrations; Disab | 2012 |
Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathy.
Topics: Cardiomyopathy, Dilated; Carnitine; Chromosome Aberrations; Diagnosis, Differential; Echocardiograph | 2004 |
Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Chromosome Aberrations; Developmental Di | 2005 |
L-Carnitine protects mammalian cells from chromosome aberrations but not from inhibition of cell proliferation induced by hydrogen peroxide.
Topics: Animals; Carnitine; Cell Proliferation; CHO Cells; Chromosome Aberrations; Cricetinae; Cricetulus; D | 2005 |
The protective effect of L-carnitine in peripheral blood human lymphocytes exposed to oxidative agents.
Topics: Carnitine; Chromosome Aberrations; Comet Assay; Humans; Hydrogen Peroxide; Lymphocytes; Oxidants; Ox | 2006 |
L-carnitine enhances resistance to oxidative stress by reducing DNA damage in Ataxia telangiectasia cells.
Topics: Ataxia Telangiectasia; Carnitine; Cell Cycle; Cell Line; Chromosome Aberrations; Comet Assay; DNA Da | 2008 |
Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes.
Topics: Acids; Blotting, Western; Brain Diseases, Metabolic; Carnitine; Chromatography, Gas; Chromosome Aber | 1990 |
Familial carnitine deficiency: further evidence for autosomal recessive transmission with variable expression.
Topics: Carnitine; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Female; Gene Expression R | 1988 |