ライフサイエンスコーパス: Thlaspi

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1 orming protein (TFP) from field-penny cress, Thlaspi arvense (Brassicaceae), is a representative of s

2 Thlaspi caerulescens and the nonaccumulators Thlaspi arvense and Thlaspi perfoliatum.

3 Field pennycress (Thlaspi arvense L.) has potential as an oilseed crop tha

4 goesingense and the non-accumulator species Thlaspi arvense revealed no major differences in the coo

5 in the nonaccumulators Arabidopsis thaliana, Thlaspi arvense, and Brassica juncea.

6 aerulescens and in a related nonaccumulator, Thlaspi arvense, showed that alteration in the regulatio

7 In comparison with Thlaspi arvense, Thlaspi caerulescens (a heavy metal acc

8 aerulescens, and the related non-accumulator Thlaspi arvense.

9 In comparison with Thlaspi arvense, Thlaspi caerulescens (a heavy metal accumulator) can gro

10 nse, Thlaspi rosulare, Thlaspi oxyceras, and Thlaspi caerulescens and the nonaccumulators Thlaspi arv

11 Thlaspi caerulescens is a heavy metal hyperaccumulator p

12 Noccaea caerulescens (formerly known as Thlaspi caerulescens), an extremophile heavy metal hyper

13 The ability of Thlaspi caerulescens, a zinc (Zn)/cadmium (Cd) hyperaccu

14 of heavy metal accumulation was conducted in Thlaspi caerulescens, a Zn/Cd-hyperaccumulating plant sp

15 s in the Zn/Cd hyperaccumulator model plant, Thlaspi caerulescens, and the related non-accumulator Th

16 ies, Noccaea caerulescens, formerly known as Thlaspi caerulescens.

17 A number of Thlaspi genes that conferred Cd tolerance to yeast were

18 evolution of metal hyperaccumulation in the Thlaspi genus.

19 ein 1 (MTP1) from the Ni/Zn hyperaccumulator Thlaspi goesingense (TgMTP1), in the Saccharomyces cerev

20 When growing in its native habitat, Thlaspi goesingense can hyperaccumulate 1.2% of its shoo

21 The integral membrane protein Thlaspi goesingense metal tolerance protein 1 (TgMTP1) h

22 The ability of Thlaspi goesingense to hyperaccumulate Ni seems to be go

23 s collected from serpentine soils, including Thlaspi goesingense, T. oxyceras, and T. rosulare, and n

24 nvestigated, including the hyperaccumulators Thlaspi goesingense, Thlaspi rosulare, Thlaspi oxyceras,

25 e histidine (His) in Ni hyperaccumulation in Thlaspi goesingense, we investigated the regulation of H

26 A detailed characterization of the Thlaspi heavy metal ATPase, TcHMA4, demonstrated that it

27 f nickel (Ni)/zinc (Zn) hyperaccumulation in Thlaspi; however, the molecular signaling pathways that

28 the ability to hyperaccumulate Ni in various Thlaspi hyperaccumulators collected from serpentine soil

29 tolerance to Ni-induced oxidative stress in Thlaspi Ni hyperaccumulators.

30 ators Thlaspi goesingense, Thlaspi rosulare, Thlaspi oxyceras, and Thlaspi caerulescens and the nonac

31 and the nonaccumulators Thlaspi arvense and Thlaspi perfoliatum.

32 g the hyperaccumulators Thlaspi goesingense, Thlaspi rosulare, Thlaspi oxyceras, and Thlaspi caerules

33 r of Ni hyperaccumulation in the six diverse Thlaspi species investigated, including the hyperaccumul

34 ssicaceae family members, including numerous Thlaspi species that hyperaccumulate Ni up to 3% of ther

35 Zn influx in roots of the hyperaccumulating Thlaspi species.

36 ports regarding ZNT1 regulation in these two Thlaspi species.

37 of ion transport in mesophyll cells from two Thlaspi spp. that differ significantly in their physiolo

38 kinetics is preferentially activated in each Thlaspi spp., both species have the capability to switch

39 ne-based Ni tolerance previously observed in Thlaspi, suggesting a biochemical linkage between SA and

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