354) Plant growth-promoting traits of isolate CB7 wer |
355) led that P-solubilization and other plant growth-promoting traits were dependent on |
356) asymmetry at 6 months of age and opposite growth trajectories in asymmetry over the |
357) ath achievement profiles and longitudinal growth trajectories of a nationally repres |
358) esults unveiled the detailed topology and growth trajectories of nine cortical funct |
359) liable and valid measure of posttraumatic growth among Chinese adolescents having ex |
360) milk-LNS, but not soy-LNS promotes linear growth among at-risk infants mainly betwee |
361) beneficial effects of endophytes on plant growth are important for agricultural ecos |
362) the findings that well-being and personal growth are related to the availability of |
363) such as the pitfalls of relying on viral growth as a strategy for obtaining reach a |
364) ew compound was able to suppress mycelial growth as well as the spores germination o |
365) ial characterization included analysis of growth dynamics of hCECs grown in either p |
366) ndicators of state shift in unsustainable growth dynamics. |
367) Positive mycorrhizal growth effects in grain, husk, straw, and |
368) lation of miR-106b counterbalances TGF-β growth-inhibiting effects by eliminating a |
369) g rates and lower pollen diversity in old growth forest populations. |
370) ed across adult and seed cohorts from old growth forest with lower density, secondar |
371) Growth hormone (GH) plays an important rol |
372) ion of relapse in the second patient with growth hormone secreting pituitary tumor. |
373) ining a multi-state model with the latent growth model defines a joint model which e |
374) nction over time is described by a linear growth model with random effects. |
375) ictors, were identified with latent class growth modeling. |
376) Finally, the results of growth-mixture modeling indicated that 89. |
377) on between paternal involvement and fetal growth outcomes (i.e., low birth weight [L |
378) d to examine their association with child growth outcomes. |
379) g incubation temperature, time, aeration, growth phase of the mycelium, particle siz |
380) r induction at the end of the exponential growth phase. |
381) ll clones, we monitored cancer-associated growth properties and characterized change |
382) rk has demonstrated the cell-adhesive and growth-promoting properties of the SIKVAV |
383) To fill this data gap we compared cell growth responses to SB and FC in ovarian a |
384) Therefore, the patterns of growth-climate responses and of climate va |
385) he prenatal period, resulted in postnatal growth restriction and delayed puberty in |
386) small, reflecting a high burden of fetal growth restriction and preterm birth. |
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