succinyl-coenzyme a has been researched along with Pregnancy in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (25.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Anvar, Z; Faghihi, MA; Farazi Fard, MA; Habibzadeh, P; Hafizi, A; Jamali, L; Nasr Esfahani, MH; Nikuei, P; Salarian, L; Tabatabaei, Z | 1 |
Jerome-Majewska, LA; Moreno-Garcia, MA; Rosenblatt, DS | 1 |
Bicakci, Z | 1 |
Brand, MD; Ferre, P; Girard, J; Quant, PA; Robin, D; Robin, P | 1 |
1 review(s) available for succinyl-coenzyme a and Pregnancy
Article | Year |
---|---|
Vitamin B(12) metabolism during pregnancy and in embryonic mouse models.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Acyl Coenzyme A; Animals; Disease Models, Animal; Embryonic Development; Female; Homocysteine; Humans; Methionine; Methylmalonyl-CoA Mutase; Mice; Pregnancy; Vitamin B 12; Vitamin B 12 Deficiency | 2013 |
3 other study(ies) available for succinyl-coenzyme a and Pregnancy
Article | Year |
---|---|
Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene.
Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Child; Female; High-Throughput Nucleotide Sequencing; Homozygote; Humans; Infant; Infant, Newborn; Iran; Male; Methylmalonyl-CoA Mutase; Mutation, Missense; Phenotype; Pregnancy; Preimplantation Diagnosis | 2020 |
Growth retardation, general hypotonia, and loss of acquired neuromotor skills in the infants of mothers with cobalamin deficiency and the possible role of succinyl-CoA and glycine in the pathogenesis.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Anemia; Female; Gluconeogenesis; Glycine; Growth Disorders; Hematopoiesis; Humans; Infant; Male; Mothers; Motor Skills; Muscle Hypotonia; Nervous System Diseases; Pregnancy; Pregnancy Complications; Vitamin B 12; Vitamin B 12 Deficiency | 2015 |
Control of hepatic mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase during the foetal/neonatal transition, suckling and weaning in the rat.
Topics: Acyl Coenzyme A; Aging; Animals; Animals, Newborn; Enzyme Activation; Female; Fetus; Glucagon; Hydroxymethylglutaryl-CoA Synthase; Ketone Bodies; Mitochondria, Liver; Oxygen Consumption; Pregnancy; Rats; Rats, Inbred Strains; Weaning | 1991 |