- 同
- retinoic acid receptor a
WordNet
- (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
- informal term for information; "give me the gen on your new line of computers"
PrepTutorEJDIC
- 遺伝子
- Regular Army正規軍
UpToDate Contents
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English Journal
- Characterization of wheat-Secale africanum chromosome 5Ra derivatives carrying Secale specific genes for grain hardness.
- Li G1, Gao D1, La S1, Wang H1, Li J1, He W1, Yang E2, Yang Z3.
- Planta.Planta.2016 Feb 16. [Epub ahead of print]
- MAIN CONCLUSION: New wheat- Secale africanum chromosome 5R a substitution and translocation lines were developed and identified by fluorescence in situ hybridization and molecular markers, and chromosome 5R a specific genes responsible for grain hardness were isolated. The wild species, Secale afric
- PMID 26883668
- Fusion genes in malignant neoplastic disorders of haematopoietic system.
- Saleem M, Yusoff NM.
- Hematology (Amsterdam, Netherlands).Hematology.2016 Feb 12. [Epub ahead of print]
- Objectives The new World Health Organization's (WHO) classification of haematopoietic and lymphoid tissue neoplasms incorporating the recurrent fusion genes as the defining criteria for different haematopoietic malignant phenotypes is reviewed. The recurrent fusion genes incorporated in the new WHO'
- PMID 26871368
- Rapid diagnosis of acute promyelocytic leukemia with the PML-RARA fusion gene using a combination of droplet-reverse transcription-polymerase chain reaction and instant-quality fluorescence in situ hybridization.
- Shigeto S1, Matsuda K2, Yamaguchi A3, Sueki A1, Uehara M3, Sugano M1, Uehara T1, Honda T1.
- Clinica chimica acta; international journal of clinical chemistry.Clin Chim Acta.2016 Jan 30;453:38-41. doi: 10.1016/j.cca.2015.12.001. Epub 2015 Dec 2.
- BACKGROUND: Acute promyelocytic leukemia (APL) with the PML-RARA fusion gene can be effectively cured using molecular-targeted therapies, which require both detection and quantification of the PML-RARA fusion gene. Here, we developed a rapid assay for identifying and measuring the PML-RARA fusion ge
- PMID 26656442
Japanese Journal
- 初発時に中枢神経浸潤を合併した急性前骨髄球性白血病
- 自己免疫性肝炎による門脈圧亢進症症例にall-trans-retinoic acidが有効であった急性前骨髄球性白血病
Related Links
- Complete information for RARA gene (Protein Coding), Retinoic Acid Receptor, Alpha, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium ... Retinoic acid ...
- acute promyelocytic leukemia - caused by mutations in the RARA gene Gene mutations can be acquired during a person's lifetime and are present only in certain cells. These mutations are called somatic mutations, and they are not ...
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- 関
- See Retinoic acid receptor