ライフサイエンスコーパス: double deletion mutant

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1 d-type lysozyme with a higher catalytic rate double deletion mutant.

2 with a single deletion in speA or speC and a double deletion mutant.

3 effect is abolished in the N- and C-terminal double deletion mutant.

4 (SRPK1) complements the growth defect of the double-deletion mutant.

5 o create diploid strains that are homozygous double-deletion mutants.

6 Using a double-deletion mutant (12203) of CPXV, we show that dir

7 The DeltaptlEDeltaptlD double deletion mutant accumulated 12, the substrate for

8 The double deletion mutant also exhibited substantially redu

9 The nhaA nhaB double deletion mutant also showed inhibited growth in a

10 Double deletion mutants also display phenotypes associat

11 The colonies of the rbmC bap1 double deletion mutant and bap1 single deletion mutant e

12 nvolved construction of isogenic single- and double-deletion mutants and inoculation of 9-day-old F4a

13 80% of the wild-type apoA-I control value by double deletion mutants apoA-I[delta(1-41)delta(185-243)

14 Expression of this double-deletion mutant as a glutathione S-transferase fu

15 We find that a double deletion mutant (Delta ces1 Delta ces4 ) grows at

16 d to plasma and wild-type apoA-I, and in the double deletion mutants, Delta(1-41, 185-243) and Delta(

17 t activate NF-kappaB in cells expressing the double deletion mutant Delta133-224/Delta372-419.

18 f a moderate magnitude were recovered by the double deletion mutant Delta671-690/Delta720-765.

19 A double deletion mutant (DeltasisA DeltasisB) resulted in

20 ast to the single mutants, the robA and nudG double deletion mutant exhibits a severe nud phenotype a

21 f NPC1, ncr-1 and ncr-2, and an ncr-2; ncr-1 double deletion mutant forms dauer larvae constitutively

22 ored the survival of the Y. pestis nhaA nhaB double deletion mutant in blood.

23 ular lysophospholipase activity, a plb1/plb2 double deletion mutant is completely devoid of lysophosp

24 ts display wild-type conidial germination, a double-deletion mutant is delayed in germination in resp

25 Double deletion mutants lacking pgpA and pgpB are viable

26 osystem I-less background strain, and also a double-deletion mutant lacking both plastocyanin and cyt

27 The double deletion mutant of apoA-I had reduced thermal and

28 m, the endotoxicity and CAMP resistance of a double deletion mutant of lpxE-eptA was similar to that

29 The WT apoA-I, amino, carboxy and double deletion mutants of apoA-I showed differences in

30 ss-linking of WT apoA-I, amino-terminal, and double deletion mutants of apoA-I to ABCA1 showed simila

31 y analysis of gene expression in single- and double-deletion mutants of each protein to identify thei

32 Cultures of the p53 double deletion mutant ovarian cell line SK-OV-3 were in

33 ith a T3SS1 deletion mutant or a T3SS1 T3SS2 double deletion mutant produced no mortality.

34 Analyses of ert-m and ant1 single- and double-deletion mutants suggest Ant1 as a closely linked

35 or the wild-type RNA is 60 degreesC; for the double-deletion mutant U2653Delta/C2667Delta it is 65 de

36 The resulting double deletion mutant virus strain, dl5-29, fails to fo

37 Furthermore, the rbmC bap1 double deletion mutant was unable to form biofilms at th

38 A menF dhbC double-deletion mutant was both MK and DHB deficient.

39 ence in a mouse peritonitis model, whereas a double-deletion mutant was highly attenuated (P<.004) ve

40 ccharomyces cerevisiae) vps23Delta bro1Delta double-deletion mutant, we showed that the Vps23p ESCRT-

41 an rescue the lethal phenotype of a min slmA double deletion mutant, which we think is due to the eli

42 The double deletion mutant with deletions in both copies of

43 The construction of the double deletion mutant without Arg208His209 and its NMR

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