adenine has been researched along with Severe Combined Immunodeficiency in 2 studies
Severe Combined Immunodeficiency: Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Minegishi, Y | 1 |
| Ishii, N | 1 |
| Maeda, H | 1 |
| Takagi, S | 1 |
| Tsuchida, M | 1 |
| Okawa, H | 1 |
| Sugamura, K | 1 |
| Yata, J | 1 |
| Kanai, N | 1 |
| Yanai, F | 1 |
| Hirose, S | 1 |
| Nibu, K | 1 |
| Izuhara, K | 1 |
| Tani, T | 1 |
| Kubota, T | 1 |
| Mitsudome, A | 1 |
2 other studies available for adenine and Severe Combined Immunodeficiency
| Article | Year |
|---|---|
Three novel mutations in the interleukin-2 receptor gamma chain gene in four Japanese patients with X-linked severe combined immunodeficiency.
Topics: Adenine; Base Sequence; Cytosine; DNA Primers; Female; Humans; Japan; Macromolecular Substances; Mal | 1995 |
A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G-->A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency.
Topics: Adenine; Alternative Splicing; Base Sequence; Exons; Frameshift Mutation; Guanine; Humans; Infant; M | 1999 |