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exon
ЭКЗОНЫ
Last Update: 2014-12-09
Usage Frequency: 9
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
vdj exon
vdj ekzon
Last Update: 2014-12-09
Usage Frequency: 1
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
exon, vdj
vdj ekzon
Last Update: 2014-12-09
Usage Frequency: 1
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
hinge exon
ekzony prikrepliaiushchie
Last Update: 2014-12-09
Usage Frequency: 1
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
exon, hinge
ekzony prikrepliaiushchie
Last Update: 2014-12-09
Usage Frequency: 1
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
exon (finding)
ekzony
Last Update: 2014-12-09
Usage Frequency: 1
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
exon non-synonymous mutation
mutatsii oshibochnye
Last Update: 2014-12-09
Usage Frequency: 1
Quality:
Warning: This alignment may be wrong.
Please delete it you feel so.
the last exon codes for more than 80% of the secreted protein.
Последний экзон более, чем на 80 % кодирует белок.
Last Update: 2016-03-03
Usage Frequency: 1
Quality:
5ht2cr is different due to possessing an imperfect inverted repeat at the end of exon 5 and the beginning of intron 5 allowing formation of an rna duplex producing the dsrna required by adars for editing.
5ht2cr is different due to possessing an imperfect inverted repeat at the end of exon 5 and the beginning of intron 5 allowing formation of an rna duplex producing the dsrna required by adars for editing.
Last Update: 2016-03-03
Usage Frequency: 1
Quality:
another editing site, site f has also been located in the exon complementary sequence (ecs) of intron 5.
another editing site, site f has also been located in the exon complementary sequence (ecs) of intron 5.
Last Update: 2016-03-03
Usage Frequency: 1
Quality:
== disease linkage ==mutations in exon 2 of the gata1 gene are present in almost all cases of down syndrome (ds)-associated acute megakaryoblastic leukemia (amkl).
Мутации в экзоне 2 гена gata1 присутствуют почти во всех случаях острого мегакариобластного лейкоза (amkl), ассоциированного с синдромом Дауна (ds).
Last Update: 2016-03-03
Usage Frequency: 1
Quality: