neurokinin b has been researched along with Adrenal Gland Hypofunction in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Atsumi, T; Chida, D; Kameda, H; Kondo, T; Miyoshi, H; Nagai, S; Nakamura, A; Shimizu, C | 1 |
| Bakiri, F; Brauner, R; Chaouachi, B; Chaussain, JL; de Laët, MH; Hadj-Rabia, S; Hannachi, R; Lyonnet, S; Munnich, A; Pelet, A; Penet, C; Rotschild, A; Salomon, R | 1 |
2 other study(ies) available for neurokinin b and Adrenal Gland Hypofunction
| Article | Year |
|---|---|
Expression and regulation of neuromedin B in pituitary corticotrophs of male melanocortin 2 receptor-deficient mice.
Topics: Adrenal Insufficiency; Animals; Corticosterone; Corticotrophs; Corticotropin-Releasing Hormone; Dexamethasone; Gene Expression Profiling; Gene Expression Regulation; Glucocorticoids; Immunohistochemistry; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Neurokinin B; Oligonucleotide Array Sequence Analysis; Pituitary Gland; Pro-Opiomelanocortin; Receptor, Melanocortin, Type 2; Reverse Transcriptase Polymerase Chain Reaction | 2014 |
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome.
Topics: Adrenal Insufficiency; Africa, Northern; Alleles; Cardia; Chromosome Mapping; Chromosomes, Artificial, Mammalian; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 12; Consanguinity; Female; Genetic Testing; Genotype; Haplotypes; Humans; Lacrimal Apparatus Diseases; Linkage Disequilibrium; Male; Microsatellite Repeats; Neurokinin B; Pedigree; Physical Chromosome Mapping; Polymorphism, Genetic; Stomach Diseases; Syndrome | 2000 |