Results 191 to 200 of about 254,091 (256)

Diagnostic Odyssey of Atypical Long‐Chain 3‐Hydroxyacyl‐CoA Dehydrogenase Deficiency (LCHADD) Explained by Three Allelic Products From Two Pathogenic Variants

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) is an autosomal recessive mitochondrial defect of long‐chain fatty acid β‐oxidation, caused by biallelic pathogenic variants in HADHA or HADHB. We report a 22‐year‐old male with an atypically mild presentation of LCHADD who was referred to the Undiagnosed Diseases Network (UDN ...
Yutaka Furuta   +9 more
wiley   +1 more source

Cultivar-Specific Differences in C6 and C7 Sugar Metabolism During Avocado Ripening: Comparative Insights from <i>Bacon</i>, <i>Fuerte</i>, and <i>Hass</i>. [PDF]

open access: yesPlants (Basel)
Beiro-Valenzuela MG   +8 more
europepmc   +1 more source
Some of the next articles are maybe not open access.

Related searches:

Sugar metabolism by Brucellae

Veterinary Microbiology, 2002
The metabolic capabilities of the species of Brucella were originally of interest as a means of distinguishing them from each other and from other genera. Certain unusual characteristics, especially erythritol utilization, were studied in the hopes they would shed light on the pathogenicity.
Richard C, Essenberg   +3 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy