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1  primarily found among grandsons compared to granddaughters.
2  risk in daughters, granddaughters and great-granddaughters.
3 have accelerated tumor growth compared to CO granddaughters.
4 ve and increased intra-abdominal fat mass in granddaughters, accompanied by accelerated accumulation
5 en-induced mammary cancer risk in daughters, granddaughters and great-granddaughters.
6 dence interval [CI], 1.6-6.7), but not among granddaughters and nieces of the probands (RR, 1.2; 95%
7 ermal cell files, suggested to be daughters, granddaughters, and great-granddaughters of the direct p
8                                The two inner granddaughters attach to the somatic gonadal anchor cell
9 d with the slope of the BMI trajectory among granddaughters (beta = 0.10, 95% confidence interval: 0.
10 n grandparents' chronic poverty exposure and granddaughters' BMI growth slope remained even after con
11 ed cells composed of a mother, daughter, and granddaughter bud.
12 curred in daughters, granddaughters or great-granddaughters - but in 5% of the pedigrees cells contin
13 d with later in childhood (13-16 years), his granddaughters, but not grandsons, had evidence of exces
14 had started smoking pre-puberty, their great-granddaughters, but not great-grandsons, had excess body
15 e these techniques to show that daughter and granddaughter cells can inherit very different states, o
16 lls start to elongate, suggesting that great-granddaughter cells switch synchronously from the mitoti
17 mmetric cell divisions: only one among four "granddaughter" cells switches.
18  cattle were mapped in a very large Holstein granddaughter design.
19 evaluated empirically by analyzing simulated granddaughter designs consisting of 2000 sons, 20 relate
20 evaluated empirically by analyzing simulated granddaughter designs.
21  in mammary cancer risk is transmitted to HF granddaughters equally through the female or male germ l
22                        Further, we show that granddaughters (F2) from the OID grand-paternal germline
23 ndmaternal diet on reproductive potential of granddaughters in the absence of any further dietary man
24  length declines more rapidly in the exposed granddaughters, indicating accelerated ageing in the rep
25                                  By taking a granddaughter ion (MS3) spectrum of a particular daughte
26  quadrant founder cell, empowering its great-granddaughter macromere 3D to act as a single-celled org
27 rs of HF rat dams and in daughters and great-granddaughters of EE2 rat dams.
28 bnormalities and cancer in the daughters and granddaughters of exposed pregnant mice.
29 ry tumourigenesis is higher in daughters and granddaughters of HF rat dams and in daughters and great
30 d to be daughters, granddaughters, and great-granddaughters of the direct progeny of each stem cell.
31 es to the ablation of neighboring cells, the granddaughters of the primary op blast cell are categori
32 t phenotype generally occurred in daughters, granddaughters or great-granddaughters - but in 5% of th
33 enerate four vulF cells, while the two outer granddaughters produce four vulE progeny.
34 ters to instruct the formation of seven-tile granddaughter sequences that are identical to the initia
35 study the final position of two of its great-granddaughters, the end of migration of which was previo
36 erm lines, but it is only transmitted to EE2 granddaughters through the female germ line.
37       The second interaction induces two ABa granddaughters to become mesodermal precursors.