ライフサイエンスコーパス: dwarfing

1 mber (reduction) and whole-plant morphology (dwarfing).

2 otypes, including spontaneous cell death and dwarfing.

3 y cranial capacity cannot result from normal dwarfing.

4 ID1c silencing corresponded to the degree of dwarfing.

5 ade avoidance, causing proximity-conditional dwarfing.

6 Conversely, LOH2 overexpression resulted in dwarfing.

7 ized to understand the mechanisms underlying dwarfing.

8 sponse to gibberellin is conferred by mutant dwarfing alleles at one of two Reduced height-1 (Rht-B1

9 The most widely utilized dwarfing alleles in wheat (Triticum aestivum; e.g. Rht-B

10 sents a potential target for producing novel dwarfing alleles.

11 ion lines of M. truncatula results in severe dwarfing, altered development, reduction in lignin conte

12 Both alleles cause dwarfing and constitutive defense responses, similar to

13 D EPIDERMAL FLUORESCENCE 4 (REF4) that cause dwarfing and decreased accumulation of phenylpropanoids.

14 In contrast, the M.9 T337 rootstock is dwarfing and does not alter fire blight susceptibility o

15 ession of ABI3 or ABI5 does not suppress the dwarfing and Glc dependence caused by abi8 but partially

16 tive transcriptional process responsible for dwarfing and inhibition of lignin biosynthesis, and sugg

17 4 mutant alleles suppress the ssi2-conferred dwarfing and lesion development, the NPR1-independent ex

18 modifications are often also associated with dwarfing and other changes in plant growth.

19 For example, the M.7 EMLA rootstock is semi-dwarfing and reduces the susceptibility of the scion to

20 protease, the overexpression of which causes dwarfing and resistance to virulent Pseudomonas syringae

21 effects, including but not limited to severe dwarfing appearance, chlorosis, nearly complete reductio

22 ains than would be predicted from a model of dwarfing based on the intraspecific scaling of the mainl

23 Two dwarfing candidate genes, homeologues of dw3 of sorghum

24 cause pseudoachondroplasia (PSACH), a severe dwarfing condition that has a growth plate chondrocyte p

25 SEMD) and mapped a gene associated with this dwarfing condition to chromosome 10q23-24, a region synt

26 oachondroplasia (PSACH), a severe short-limb dwarfing condition, results from mutations that cause mi

27 onsible for achondroplasia (ACH) and related dwarfing conditions in humans.

28 lable concerning the natural history of this dwarfing disorder.

29 sembly lines can reach almost 5 megadaltons, dwarfing even the ribosome (approximately 2.6 megadalton

30 against tissue rupture was unaffected by the dwarfing gene but was consistently lower (-26%, p<0.01)

31 ors varied in this study were breeding line, dwarfing gene dose, soil type, and fertilization.

32 to identify both homeologues of the dw3 semi-dwarfing gene of Sorghum bicolor.

33 reased (-11%, p<0.025), by one allele of the dwarfing gene.

34 Of the four major dwarfing genes described in sorghum, only Dw3 has been c

35 rachydactyly type B (BDB1) and the mesomelic dwarfing in mice homozygous for a lacZ and/or a neo inse

36 rt that activation of RPP5 locus R genes and dwarfing in the bal variant are caused by a 55-kb duplic

37 st rapid and well documented cases of island dwarfing known thus far took place over thousands of yea

38 pic effects that include facial dysmorphism, dwarfing, male sterility, anemia, and cystic choroid ple

39 tropic effects including facial dysmorphism, dwarfing, male sterility, anemia, and progressive polycy

40 Here, we describe a different dwarfing mechanism found in maize brachytic2 (br2) mutan

41 Six different orthologous dwarfing mutant alleles encode proteins that are altered

42 this study, we have characterized additional dwarfing mutations in Rht-B1 and Rht-D1.

43 Here, we describe a rapid example of dwarfing of a large mammal - the feral cattle of Amsterd

44 The dwarfing of large mammals on islands has been observed b

45 ression of ACT1 in vegetative tissues causes dwarfing of plants and altered morphology of most organs

46 n, ACT1, in vegetative tissues causes severe dwarfing of plants with aberrant organization of most pl

47 Island colonization and subsequent dwarfing of Pleistocene proboscideans is one of the more

48 The dwarfing of the floral shoot internodes caused by the ga

49 ht (R) and far-red light (FR) and an overall dwarfing of the mature plant.

50 hypocotyls to R and caused even more marked dwarfing of the mature plant.

51 s, reduced stolon formation, together with a dwarfing phenotype and a lack of flowering in the most s

52 Hemizygous plants displayed a semi-dwarfing phenotype, in which stem length was reduced but

53 aling pathways of gibberellin (GA) can cause dwarfing phenotypes in plants, and the use of such mutat

54 owth, we performed a comparative analysis of dwarfing phenotypes manifested in mouse mutants lacking

55 Genetic analyses of dwarfing phenotypes resulting from targeted mutagenesis

56 mutation and to fine map a second, epistatic dwarfing QTL on sorghum chromosome 9 (Sb-HT9.1).

57 xotic lines that have been introgressed with dwarfing quantitative trait loci (QTL) from a common par

58 life span and flowering duration, sterility, dwarfing, reduced seed yield and shorter root length.

59 omes involving craniosynostosis, whereas the dwarfing syndromes are largely associated with FGFR3 mut

60 vonoid biosynthesis, resulted in less severe dwarfing than silencing of HCT alone.

61 lution', were enabled by the introduction of dwarfing traits into the plants.