carnitine has been researched along with Chromosome Deletion in 4 studies
Chromosome Deletion: Actual loss of portion of a chromosome.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Carnitine is a key molecule in energy metabolism that helps transport activated fatty acids into the mitochondria." | 1.40 | The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile. ( Akrami, SM; Rashidi-Nezhad, A; Reymond, A; Saebnouri, H; Talebi, S, 2014) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rashidi-Nezhad, A | 1 |
| Talebi, S | 1 |
| Saebnouri, H | 1 |
| Akrami, SM | 1 |
| Reymond, A | 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 |
| Rodrigues Pereira, R | 1 |
| van Ede, CM | 1 |
| Beemer, FA | 1 |
| Maegawa, GH | 1 |
| Poplawski, NK | 1 |
| Andresen, BS | 1 |
| Olpin, SE | 1 |
| Nie, G | 1 |
| Clarke, JT | 1 |
| Teshima, I | 1 |
1 review available for carnitine and Chromosome Deletion
| Article | Year |
|---|---|
Interstitial deletion of 1p22.2p31.1 and medium-chain acyl-CoA dehydrogenase deficiency in a patient with global developmental delay.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Chromosome Deletion; Chromosomes, Human, Pair 1; Dicarboxy | 2008 |
3 other studies available for carnitine and Chromosome Deletion
| Article | Year |
|---|---|
The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile.
Topics: Abnormalities, Multiple; Calcinosis; Carnitine; Carrier Proteins; Child, Preschool; Chromosome Delet | 2014 |
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 |
Successful carnitine therapy for Raynaud's phenomenon in velo-cardio-facial syndrome.
Topics: Abnormalities, Multiple; Adolescent; Carnitine; Chromosome Deletion; Chromosomes, Human, Pair 22; Fe | 2003 |