nad has been researched along with Abnormalities, Congenital in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 2 (28.57) | 2.80 |
| Authors | Studies |
|---|---|
| Bozon, K; Bröer, S; Cuny, H; Dunwoodie, SL; Kirk, RB; Sheng, DZ | 1 |
| Bi, W; Campagnolo, C; Cao, Y; Chapman, G; Choy, KW; Cuny, H; Drysdale, T; Dunwoodie, SL; Flores-Daboub, JA; Iyer, KR; Leung, TN; Liu, P; Siu, VM; Szot, JO; Westerfield, L; Xiao, R | 1 |
| Brown, MA; Chapman, G; Colley, A; Collins, F; Duncan, EL; Dunwoodie, SL; Enriquez, A; Giannoulatou, E; Guillemin, GJ; Halliday, J; Ho, JWK; Hughes, JN; Humphreys, DT; Ip, E; Kikuchi, K; Leo, PJ; Lim, CK; Maghzal, GJ; Mark, PR; Martin, EMMA; McInerney-Leo, AM; Moreau, J; Rapadas, M; Shi, H; Sillence, DO; Smith, J; Sparrow, DB; Stocker, R; Sugimoto, K; Szot, JO; Thomas, PQ; Wang, R; Winlaw, DS | 1 |
| Vander Heiden, MG | 1 |
| LANGLEY, M; SANADI, DR; SEARLS, RL | 1 |
| GASSER, G; HOLZNER, JH | 1 |
| Fratta, ID | 1 |
7 other study(ies) available for nad and Abnormalities, Congenital
| Article | Year |
|---|---|
Maternal heterozygosity of Slc6a19 causes metabolic perturbation and congenital NAD deficiency disorder in mice.
Topics: Amino Acid Transport Systems, Neutral; Animals; Congenital Abnormalities; Female; Heterozygote; Kidney; Mice; NAD; Niacinamide; Pregnancy; Tryptophan | 2023 |
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders.
Topics: Alleles; Amino Acid Sequence; Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor; Congenital Abnormalities; Female; Genotype; Gestational Age; Humans; Infant; Infant, Newborn; Male; Multiple Organ Failure; Mutation, Missense; NAD; Pedigree; Phenotype; Pregnancy; Sequence Homology | 2020 |
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
Topics: 3-Hydroxyanthranilate 3,4-Dioxygenase; Anal Canal; Animals; Congenital Abnormalities; Dietary Supplements; Disease Models, Animal; Esophagus; Female; Heart Defects, Congenital; Humans; Hydrolases; Kidney; Limb Deformities, Congenital; Male; Mice; Mice, Knockout; Mutation; NAD; Niacin; Sequence Analysis, DNA; Spine; Trachea | 2017 |
Metabolism and Congenital Malformations - NAD's Effects on Development.
Topics: Animals; Congenital Abnormalities; Humans; Metabolism, Inborn Errors; Mice; Mutation; NAD; Syndrome | 2017 |
alpha-Ketoglutaric dehydrogenase. VI. Reversible oxidation of dihydrothioctamide by diphosphopyridine nucleotide.
Topics: Coenzymes; Congenital Abnormalities; Ketoglutarate Dehydrogenase Complex; NAD; Oxidation-Reduction; Oxidoreductases; Vitamin A; Vitamin K; Vitamins | 1959 |
[BILATERAL APLASIA OF THE DUCTUS DEFERENS. ENZYMATIC HISTOCHEMICAL STUDY OF THE TESTES].
Topics: Adenosine Triphosphate; Biopsy; Clinical Enzyme Tests; Congenital Abnormalities; Dihydrolipoamide Dehydrogenase; Histocytochemistry; Humans; Male; NAD; Spermatozoa; Succinate Dehydrogenase; Testis; Vas Deferens | 1964 |
Nicotinamide deficiency and thalidomide: potential teratogenic disturbances in Long-Evans rats.
Topics: Abnormalities, Drug-Induced; Adrenal Cortex Hormones; Animal Feed; Animals; Birth Weight; Chlorpromazine; Congenital Abnormalities; Deficiency Diseases; Female; Fertility; Fetal Death; Fetal Diseases; Gestational Age; Liver; NAD; Niacinamide; Pregnancy; Pregnancy Complications; Rats; Rodent Diseases; Species Specificity; Thalidomide | 1969 |