ライフサイエンスコーパス: gigantism

1 ze than their mainland counterparts (insular gigantism).

2 (tg) STAT5(Deltahep) animals did not display gigantism.

3 tiny-flowered ancestors in a burst of floral gigantism.

4 ns in these genes extend life span and cause gigantism.

5 ice give opposite phenotypes of dwarfism and gigantism.

6 ficant role in the evolution of baleen whale gigantism.

7 in efficiency with body size, enabling their gigantism.

8 ent in amphibians, which mostly tend towards gigantism.

9 lutionary tree and acted as an exaptation to gigantism.

10 acromegaly in adults; the genetic causes of gigantism and acromegaly are poorly understood.

11 shing disease, growth hormone excess causing gigantism and acromegaly, clinically non-functioning ade

12 ogy could help to explain the iconic shark's gigantism and eventual demise during the Pliocene.

13 Madagascan species is known for extreme web gigantism and for producing the world's toughest biomate

14 osite to those of p27-deficient mice such as gigantism and gonadal hyperplasia.

15 alternative life-history trajectory in which gigantism and high fecundity in normally productive coas

16 Thus, we crossed a mouse model of gigantism and inflammatory liver cancer caused by hypera

17 (X-LAG) is the most severe form of pituitary gigantism and is characterized by aggressive growth horm

18 growth anomalies, including gender-specific gigantism and organomegaly.

19 es of samples obtained from 43 patients with gigantism and then sequenced an implicated gene in sampl

20 These mice develop gigantism and widespread organomegaly.

21 These evolutionary features, added to gigantism and wing reduction, make the extinct Rodrigues

22 nd the necessary hydraulics to enable floral gigantism and/or high reproductive output.

23 ecological niche migration, "pre-extinction gigantism", and photosymbiont bleaching prior to extinct

24 al change, interspecific crossability, sperm gigantism, and divergence times of the subgroup is discu

25 ontids, underwent four independent events of gigantism, and in some lineages size increased by nearly

26 y shape, reproductive investment linked with gigantism, and lepidosaurian viviparity, in which a 'ves

27 sted that Paleozoic hyperoxia enabled animal gigantism, and the subsequent hypoxia drove a reduction

28 ry hyperplasia is induced but IGF-1 rise and gigantism are blunted by puberty.

29 Although dinosaurs and gigantism are practically synonymous, an analysis of bod

30 ic pattern and possible drivers of pterosaur gigantism are uncertain.

31 liana evolution uncoupled from xylem conduit gigantism, as well as high plasticity and cell type dive

32 s related to the evolutionary cascade toward gigantism even though some titanosaurians were the large

33 Gigantism has been linked to hyperoxic conditions becaus

34 creased secretion of growth hormone leads to gigantism in children and acromegaly in adults; the gene

35 inomas, which cause acromegaly in adults and gigantism in children, and 4% are corticotropinomas, whi

36 ar phylogeny, we provide evidence of genomic gigantism in chloroviruses and show that a subset of vir

37 The evolution of gigantism in extinct otodontid sharks was paralleled by

38 Widespread gigantism in late Paleozoic insects and other arthropods

39 on of a putative syntelog for multiple organ gigantism in legumes.

40 y size, ultimately enabling the evolution of gigantism in multiple lineages.

41 st endothermy was one of the key drivers for gigantism in O. megalodon and other lamniform sharks.

42 Island faunas can be characterized by gigantism in small animals and dwarfism in large animals

43 d in insular populations of vertebrates from gigantism in small species to dwarfism in large species.

44 years ago with the dramatic demonstration of gigantism in the SOCS2-knockout mouse.

45 ially an evolutionary innovation that led to gigantism in this lineage [1].

46 an giants, but that condition cannot explain gigantism in Triassic ichthyosaurs.

47 etic analysis suggests parallel evolution of gigantism in Triassic sauropterygians.

48 Leaf gigantism in waterlilies may have been driven by selecti

49 l traits evolved near the origin of sauropod gigantism, including both rapid and uninterrupted growth

50 ce and prey quality to demonstrate how whale gigantism is driven by the interplay of prey abundance a

51 d that the magnitude of insular dwarfism and gigantism is mediated by climate as well as island size

52 Thus, genome gigantism is not restricted to a specific host or phylog

53 ver of SOCS3, suggesting a mechanism for the gigantism observed in SOCS2 transgenic mice.

54 hed a large size, demonstrating that tadpole gigantism occurred among stem-anurans.

55 n particular, extreme size change leading to gigantism occurred within the dinosaurs on multiple occa

56 volutionary contingencies better explain the gigantism of the double coconut than unusually high rate

57 ation played in the ecology and evolution of gigantism of these and associated dinosaurs.

58 some Xq26.3 in samples from 13 patients with gigantism; of these samples, 4 were obtained from member

59 diversification and the evolution of extreme gigantism over shorts timescales.

60 e gene modified in the Simpson-Golabi-Behmel gigantism/overgrowth syndrome (SGBS), is shown to span m

61 lication and is characterized by early-onset gigantism resulting from an excess of growth hormone.

62 Bulk filter feeding has enabled gigantism throughout evolutionary history.

63 The first is through axon gigantism: using axons several times larger in diameter

64 This demonstrates that polychaete gigantism was already a phenomenon in the Palaeozoic, so

65 (300 million years ago), a time when insect gigantism was widespread.

66 the Azhdarchoidea(4), a clade that exhibits gigantism, we test the hypothesis that there was a decre

67 Of the patients with gigantism who did not carry an Xq26.3 microduplication,

68 rats altered AIP induces elevated IGF-1 and gigantism, with pituitary hyperplasia through blocking t