287) In many circumstances, debates about human rights and HIV/AIDS are premised on |
288) ly assessing how an obligation to protect human rights might limit or support a stat |
289) Evidence from human studies as well as animal models hav |
290) election of formulation before animal and human studies. |
291) Thirty-two dentin specimens prepared from human third molars were divided into two g |
292) Ninety freshly extracted human third molars were used for the study |
293) ibution and thermally induced stresses of human tooth under CO2 pulsed laser beam. |
294) nt obtained from a duly donated extracted human tooth. |
295) Efforts to model the human upper respiratory system have underg |
296) ainfluenzae is a common inhabitant of the human upper respiratory tract of the norma |
297) sues and of their possible effects in the human (and animal) body is required for th |
298) investigate task-dependent activations of human AC. |
299) constructs generated by combining primary human ACs with human bone marrow MSCs (BM- |
300) This was done by locally injecting human ADRCs into an injured site after lac |
301) enhances the cardioprotective effects of human AECs. |
302) The supporting activities of DPSCs for human CB-derived CD34(+) and CD34(-) HSCs |
303) d efficiently inhibits all three purified human CDC25 isoforms (IC50 1-9 µM) in a |
304) Human DFATs were isolated from the submand |
305) investigated whether an HC diet increases human ER-positive breast cancer progressio |
306) Thus, differences between the species of human ESCs and ESCs of this non-human prim |
307) Human EnSCs seeded on 3D nanofibrous silk- |
308) Human FBXO10, an evolutionarily conserved |
309) of abnormalities likely to be present in human FXS. |
310) expression level of MMP-1, -2, and -9 in human HT1080 fibrosarcoma cells. |
311) f a computational model which resembles a human LV. |
312) lity 5a1 (Mcs5a1), which is concordant to human MCS5A1 breast cancer risk locus, med |
313) and DBT (5 - 0.05 µM) in highly enriched human NK cells, a monocyte-depleted prepar |
314) Human PCA LNCaP and PC3 cells were exposed |
315) s of CUX1 in a distinct subset of TAMs in human PDAC tissues. |
316) ion, most of the neonatal adipocytes were human PPARγ positive. |
317) ly-delivered mouse Pdx1 (Ad-Pdx1) induced human Pdx1 expression in hAFSCs and enhanc |
318) ial genome sequence of the Ningxiang pig (Human Province), which was determined thro |
319) ence of the Shaziling pig was reported in Human Province, which was determined throu |
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