ライフサイエンスコーパス: interbreed

1 a single species into two that can no longer interbreed.

2 ic variation to impede subsequent productive interbreeding.

3 on subdivision followed by relatively recent interbreeding.

4 ressing two different TCRs were generated by interbreeding 3A9 and AND CD4+ TCR transgenic mice speci

5 ng, with phenotypic similarity and extensive interbreeding across the southwestern contact zone and s

6 Thus, interbreeding, albeit of low magnitude, occurred among m

7 ch maintain host-specific adaptation despite interbreeding among males and females reared by differen

8 es suggests a recent past/current history of interbreeding among the Indo-Pacific Acropora species an

9 erived VEGF-A in HPV-mediated skin cancer by interbreeding an HPV8 transgenic mouse model with a cond

10 and dispersed across the planet through host interbreeding and gene flow.

11 al theory of speciation in that a barrier to interbreeding arises as a correlated effect of adaptive

12 are turning out to have limited abilities to interbreed, as if they were on the way to becoming diffe

13 These include the discovery of interbreeding between anatomically modern humans and ext

14 rent temporal and geographic contact, making interbreeding between ancient populations likely.

15 n intermediate type of cattle resulting from interbreeding between Bos taurus and Bos indicus subspec

16 Interbreeding between domesticated individuals and their

17 hypotheses, and detect regions of potential interbreeding between human and extinct hominines.

18 xity has been the recent evidence of limited interbreeding between modern humans and the Neandertals

19 rica and thousands of years after documented interbreeding between modern humans, Neandertals and Den

20 sparked controversy about the possibility of interbreeding between Neandertals and modern humans in E

21 veral instances of archaic admixture through interbreeding between the ancestors of modern non-Africa

22 Interbreeding between various Pkd1 and Pkd2 models revea

23 sequences are not silent remnants of ancient interbreeding but have measurable impacts on gene expres

24 allele has a selective advantage, even rare interbreeding can lead to its spread or fixation in late

25 During range expansions, even low levels of interbreeding can lead to massive introgression of local

26 We developed transgenic control mice by interbreeding CAN transgenic mice with mice expressing a

27 II activity in CAN mice to control levels by interbreeding CAN transgenic mice with mice expressing a

28 o the Ts65Dn mouse model of Down syndrome by interbreeding caused formation of intestinal adenomas at

29 (MEFs) expressing and lacking caveolin-1 by interbreeding Cav-1 (+/+) and Cav-1 (-/-) mice with INK4

30 n syntenic homology from human and mouse, an interbreed cross/backcross, and a strategy for isolation

31 In this study, we interbreed Cx37 and Cx40 knockout mice to generate Cx37-

32 tably, however, olive- and black-backed taxa interbreed (differentiated populations of A. flavinuchus

33 southern Levant, close in time to the likely interbreeding event with Neanderthals.

34 We conclude that in addition to later interbreeding events, the ancestors of Neanderthals from

35 In 30 heterozygote interbreeding experiments, 50 Cse1l wild-type mice and 1

36 oid social interactions and are not known to interbreed, genetic studies to date have found extremely

37 h to explore its role in prostate cancers by interbreeding IL-17 receptor C (IL-17RC)-deficient mice

38 These two taxa do not interbreed in central Siberia but are connected by a lon

39 havior, or pollinator attraction may prevent interbreeding in nature, causing reproductive isolation.

40 ly divergent source populations, followed by interbreeding in the invasive range.

41 enotyping of progeny obtained from EPCR(+/-) interbreeding indicated that EPCR(-/-) embryos died on o

42 Interbreeding is possible among Caribbean A. palmata and

43 A potential place of interbreeding is the notable Palaeolithic site of Riparo

44 By interbreeding isoform specific Rassf1a knockout mice wit

45 Interbreeding isolates were nearest neighbors on the evo

46 are random events, patterns of migration and interbreeding, mutational events, and horizontal transfe

47 We genetically tested this prediction by interbreeding Myc transgenics with mice lacking various

48 This was genetically tested by interbreeding Neu transgenics with knockouts of the thre

49 jor population expansion events resulting in interbreeding, not replacement.

50 sistent with a history in which the Denisova interbreeding occurred in mainland Asia and then spread

51 ossibly H. floresiensis, with some degree of interbreeding occurring.

52 Interbreeding of Arf-Cre females to males containing "fl

53 Interbreeding of heterozygotes resulted in progressive t

54 However, no homozygous pups were born after interbreeding of heterozygous mice.

55 however, no homozygous pups were born after interbreeding of heterozygous mice.

56 Interbreeding of Iqgap2(-/-) mice into the Iqgap1(-/-) b

57 al to act as an isolating barrier to prevent interbreeding of populations through a role in species r

58 Interbreeding of the extl3-mutant zebrafish (box) with T

59 ixture linkage disequilibrium created in the interbreeding of the two parental populations.

60 Interbreeding of the VISTA-deficient mice with 2D2 T-cel

61 Interbreeding of these first generation progeny resulted

62 ort the use of a sperm-specific promoter and interbreeding of transgenic and gene knockout mice for g

63 c caste determination (GCD) generated by the interbreeding of two distinct yet interdependent lineage

64 rope, and their replacement (with or without interbreeding) of the preceding "archaic" populations in

65 es an example of the missing link between an interbreeding population and isolated species.

66 to eliminate genetic incompatibilities from interbreeding populations.

67 with the evolution of behavioral barriers to interbreeding; postmating isolation usually evolves much

68 rrier and the terminal forms coexist without interbreeding, provides a situation in which variation i

69 s, phylogenetics and evaluation of potential interbreeding taxa of a species, various loci have serve

70 e both Hexa and Hexb genes disrupted through interbreeding Tay-Sachs (Hexa-/-) and Sandhoff (Hexb-/-)

71 ted mice carrying both receptor mutations by interbreeding the ActRIIA and ActRIIB knockout mutants.

72 Interbreeding the Rspo2(Tg) and Lrp6(-) alleles resulted

73 Interbreeding these mice with the cre-reporter strain, R

74 Interbreeding to a reporter strain that expresses Cre-de

75 between populations is sufficient to prevent interbreeding when the populations reunite, even in the

76 e from Prunus avium, a species that does not interbreed with P. tenella and, except for just one amin

77 etion mutant animals in the proepicardium by interbreeding with a Cre-expressing mouse that targets c

78 the genus Homo: did they go extinct without interbreeding with anatomically modern humans, or are th

79 dern human genomes retain DNA inherited from interbreeding with archaic hominins, such as Neandertals

80 pulations introgressed via relatively recent interbreeding with hominin forms that diverged from the

81 ritical source of genome diversity, although interbreeding with local wolf populations clearly occurr

82 oay sheep, possibly as a consequence of past interbreeding with modern domestic breeds.

83 of our species, Homo sapiens, including its interbreeding with other hominins, such as Neanderthals,

84 prevented by injections of anti-TNF Abs, or interbreeding with TNF receptor-deficient mice.

85 important problem in many ecosystems due to interbreeding with wild conspecifics.

86 often infested with feral weedy rice, which interbreeds with the crop; and (4) self-compatible sorgh