ライフサイエンスコーパス: chromosome engineering

1 be valuable materials for gene targeting and chromosome engineering.

2 6 in mice using Cre/loxP-mediated long-range chromosome engineering.

3 s, in vivo synthetic lethality screening and chromosome engineering.

4 ession, protein localization, epistasis, and chromosome engineering.

5 el of a human deletion syndrome generated by chromosome engineering.

6 s in vertebrates and as a tool for mammalian chromosome engineering.

7 Using a rapid strategy for Cre-loxP chromosome engineering, a deletion of approximately 370

8 nt on the X chromosome of D. melanogaster by chromosome engineering and found that, although the dele

9 is possible to use retroviral gene delivery, chromosome engineering and inducible transgenes to selec

10 Here we have used a combination of chromosome engineering and P1 artificial chromosome tran

11 As new technologies such as chromosome engineering and the creation of transchromoso

12 ation methods in plants will potentiate many chromosome engineering applications.

13 Recent advances in chromosome engineering are now allowing us to create pre

14 the vector can be used for Cre- loxP -based chromosome engineering as well as single knockouts.

15 ch expands the application of Cre-loxP-based chromosome engineering because it not only allows the co

16 In vivo chromosome engineering can be potentially used to achiev

17 have developed three new mouse models using chromosome engineering carrying the genotypes of Dp(10)1

18 Chromosome engineering combines the power of gene target

19 The term "chromosome engineering" describes technologies in which

20 Here, we report an improved scheme of chromosome engineering for efficient elimination of a la

21 Targeted chromosome engineering has facilitated the development o

22 ions, and inversions) into the mouse genome (chromosome engineering) has been established.

23 tion system has been developed for efficient chromosome engineering in Escherichia coli by using elec

24 a highly efficient recombination system for chromosome engineering in Escherichia coli was described

25 is study has demonstrated great potential of chromosome engineering in genome manipulation for plant

26 Chromosome engineering in mice enables the construction

27 Here we use chromosome engineering in mice to show that a single ext

28 9 multiplexing, as well as opportunities for chromosome engineering in the context of hepatobiliary t

29 Chromosome engineering is a major focus in the fields of

30 Chromosome engineering is a useful strategy for transfer

31 his system will be especially useful for the chromosome engineering of large heterologous fragment in

32 The results will facilitate directed chromosome engineering producing agronomically desirable

33 e a public resource (Mutagenic Insertion and Chromosome Engineering Resource; MICER) for high-through

34 We used mutagenic insertion chromosome engineering resources to generate the Plp1dup

35 We have developed a chromosome engineering strategy that allows the generati

36 We have used a mouse chromosome engineering strategy to create a null mutatio

37 We have used a chromosome engineering strategy to identify a human auto

38 Finally, using a chromosome engineering strategy, we show that only a sub

39 Another chromosome engineering success is the conversion of meio

40 des a basis to use autopolyploidization as a chromosome engineering technique to alter the organ deve

41 Here, using chromosome engineering technology, we delete in the germ

42 This new form of chromosome engineering, termed recombineering, has many

43 This review examines recent innovations in chromosome engineering that promise to greatly increase

44 We used chromosome engineering to create mice that were trisomic

45 -2 and Df(11)17-3] using retrovirus-mediated chromosome engineering to create nested deletions.

46 cause DS phenotypes, including CHD, we used chromosome engineering to generate a mapping panel of 7

47 egion further, we utilized Cre-loxP-mediated chromosome engineering to generate a targeted 800 kb del

48 16p11.2 CNVs in a systematic manner, we used chromosome engineering to generate mice harboring deleti

49 Here we use chromosome engineering to generate mouse models with gai

50 ring germ cell development, we used targeted chromosome engineering to generate mutants which either

51 In particular, the use of chromosome engineering to generate new trisomic mouse mo