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1 orming protein (TFP) from field-penny cress, Thlaspi arvense (Brassicaceae), is a representative of s
2 -CoA synthase from the high erucic feedstock Thlaspi arvense (Pennycress).
3 Thlaspi caerulescens and the nonaccumulators Thlaspi arvense and Thlaspi perfoliatum.
4                         Seeds of pennycress (Thlaspi arvense L.) an oilseed cover crop, were scanned
5                            Field pennycress (Thlaspi arvense L.) has potential as an oilseed crop tha
6 ium sativum L., 1753, Sinapis alba L., 1753, Thlaspi arvense L., 1753, and Thlaspi arvense-heat inact
7  goesingense and the non-accumulator species Thlaspi arvense revealed no major differences in the coo
8 dy of 207 natural lines of field pennycress (Thlaspi arvense) that were grown in a common environment
9 irst insights into the defense mechanisms of Thlaspi arvense, a rising crop and model species, and de
10 in the nonaccumulators Arabidopsis thaliana, Thlaspi arvense, and Brassica juncea.
11 aerulescens and in a related nonaccumulator, Thlaspi arvense, showed that alteration in the regulatio
12                           In comparison with Thlaspi arvense, Thlaspi caerulescens (a heavy metal acc
13 alba L., 1753, Thlaspi arvense L., 1753, and Thlaspi arvense-heat inactivated and three major chemica
14 aerulescens, and the related non-accumulator Thlaspi arvense.
15          In comparison with Thlaspi arvense, Thlaspi caerulescens (a heavy metal accumulator) can gro
16 nse, Thlaspi rosulare, Thlaspi oxyceras, and Thlaspi caerulescens and the nonaccumulators Thlaspi arv
17                                              Thlaspi caerulescens is a heavy metal hyperaccumulator p
18      Noccaea caerulescens (formerly known as Thlaspi caerulescens), an extremophile heavy metal hyper
19                               The ability of Thlaspi caerulescens, a zinc (Zn)/cadmium (Cd) hyperaccu
20 of heavy metal accumulation was conducted in Thlaspi caerulescens, a Zn/Cd-hyperaccumulating plant sp
21 s in the Zn/Cd hyperaccumulator model plant, Thlaspi caerulescens, and the related non-accumulator Th
22 ies, Noccaea caerulescens, formerly known as Thlaspi caerulescens.
23                                  A number of Thlaspi genes that conferred Cd tolerance to yeast were
24  evolution of metal hyperaccumulation in the Thlaspi genus.
25 ein 1 (MTP1) from the Ni/Zn hyperaccumulator Thlaspi goesingense (TgMTP1), in the Saccharomyces cerev
26          When growing in its native habitat, Thlaspi goesingense can hyperaccumulate 1.2% of its shoo
27                The integral membrane protein Thlaspi goesingense metal tolerance protein 1 (TgMTP1) h
28                               The ability of Thlaspi goesingense to hyperaccumulate Ni seems to be go
29 s collected from serpentine soils, including Thlaspi goesingense, T. oxyceras, and T. rosulare, and n
30 nvestigated, including the hyperaccumulators Thlaspi goesingense, Thlaspi rosulare, Thlaspi oxyceras,
31 e histidine (His) in Ni hyperaccumulation in Thlaspi goesingense, we investigated the regulation of H
32           A detailed characterization of the Thlaspi heavy metal ATPase, TcHMA4, demonstrated that it
33 f nickel (Ni)/zinc (Zn) hyperaccumulation in Thlaspi; however, the molecular signaling pathways that
34 the ability to hyperaccumulate Ni in various Thlaspi hyperaccumulators collected from serpentine soil
35  tolerance to Ni-induced oxidative stress in Thlaspi Ni hyperaccumulators.
36 ators Thlaspi goesingense, Thlaspi rosulare, Thlaspi oxyceras, and Thlaspi caerulescens and the nonac
37  and the nonaccumulators Thlaspi arvense and Thlaspi perfoliatum.
38 g the hyperaccumulators Thlaspi goesingense, Thlaspi rosulare, Thlaspi oxyceras, and Thlaspi caerules
39 r of Ni hyperaccumulation in the six diverse Thlaspi species investigated, including the hyperaccumul
40 ssicaceae family members, including numerous Thlaspi species that hyperaccumulate Ni up to 3% of ther
41 ports regarding ZNT1 regulation in these two Thlaspi species.
42  Zn influx in roots of the hyperaccumulating Thlaspi species.
43 of ion transport in mesophyll cells from two Thlaspi spp. that differ significantly in their physiolo
44 kinetics is preferentially activated in each Thlaspi spp., both species have the capability to switch
45 ne-based Ni tolerance previously observed in Thlaspi, suggesting a biochemical linkage between SA and