1  vs. clearance): warm- (22-28 degrees C) and cold-acclimated (13-19 degrees C) tadpoles had fewer par

2 not cold acclimate, whereas Medicago falcata cold acclimated and survived -14 degrees C.

3 peratures (>23 degrees C), circuits from the cold-acclimated animals produced less-regular pyloric rh

4              A cDNA library was created from cold-acclimated bark tissue of peach and selectively pro

5                                        Under cold-acclimated conditions, mice lacking L-PGDS had elev

6 ose-rich or -deprived media, and in roots of cold-acclimated germ plasms.

7 displayed reciprocal changes concordant with cold-acclimated insulin sensitization.

8 tion rates at intermediate temperatures than cold-acclimated isolates.

9 ude transcriptional cycling in the cold, and cold-acclimated lux seedlings are sensitive to freezing

10  splice variant expression was quantified in cold-acclimated plants by quantitative RT-PCR.

11  and Mg(2+) Manipulation of pH and Mg(2+) in cold-acclimated plants is shown to cause changes similar

12 t the whole-plant level in nonacclimated and cold-acclimated plants, whereas overexpression of the al

13 freezing tolerance of both nonacclimated and cold-acclimated plants.

14 sis also increases the freezing tolerance of cold-acclimated plants.

15 freezing tolerance in both nonacclimated and cold-acclimated plants.

16 e plasma membrane of either nonacclimated or cold-acclimated rye leaves.

17 ts indicate that the freezing sensitivity of cold-acclimated sfr4 is due to its continued susceptibil

18 ing then various doses of NPY were tested in cold-acclimated Siberian hamsters while food was withhel

19 isense lines increased from -4 degrees C for cold-acclimated wild-type plants to -8 degrees C for the