戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 (tg) STAT5(Deltahep) animals did not display gigantism.
2 tiny-flowered ancestors in a burst of floral gigantism.
3 ns in these genes extend life span and cause gigantism.
4 ice give opposite phenotypes of dwarfism and gigantism.
5  acromegaly in adults; the genetic causes of gigantism and acromegaly are poorly understood.
6  Madagascan species is known for extreme web gigantism and for producing the world's toughest biomate
7 osite to those of p27-deficient mice such as gigantism and gonadal hyperplasia.
8 alternative life-history trajectory in which gigantism and high fecundity in normally productive coas
9            Thus, we crossed a mouse model of gigantism and inflammatory liver cancer caused by hypera
10  growth anomalies, including gender-specific gigantism and organomegaly.
11 es of samples obtained from 43 patients with gigantism and then sequenced an implicated gene in sampl
12                           These mice develop gigantism and widespread organomegaly.
13 al change, interspecific crossability, sperm gigantism, and divergence times of the subgroup is discu
14 ontids, underwent four independent events of gigantism, and in some lineages size increased by nearly
15 sted that Paleozoic hyperoxia enabled animal gigantism, and the subsequent hypoxia drove a reduction
16 ic pattern and possible drivers of pterosaur gigantism are uncertain.
17 liana evolution uncoupled from xylem conduit gigantism, as well as high plasticity and cell type dive
18                                              Gigantism has been linked to hyperoxic conditions becaus
19 creased secretion of growth hormone leads to gigantism in children and acromegaly in adults; the gene
20                                   Widespread gigantism in late Paleozoic insects and other arthropods
21 d in insular populations of vertebrates from gigantism in small species to dwarfism in large species.
22 years ago with the dramatic demonstration of gigantism in the SOCS2-knockout mouse.
23 ially an evolutionary innovation that led to gigantism in this lineage [1].
24 etic analysis suggests parallel evolution of gigantism in Triassic sauropterygians.
25                                 Thus, genome gigantism is not restricted to a specific host or phylog
26 ver of SOCS3, suggesting a mechanism for the gigantism observed in SOCS2 transgenic mice.
27 n particular, extreme size change leading to gigantism occurred within the dinosaurs on multiple occa
28 ation played in the ecology and evolution of gigantism of these and associated dinosaurs.
29 some Xq26.3 in samples from 13 patients with gigantism; of these samples, 4 were obtained from member
30 e gene modified in the Simpson-Golabi-Behmel gigantism/overgrowth syndrome (SGBS), is shown to span m
31 lication and is characterized by early-onset gigantism resulting from an excess of growth hormone.
32                    The first is through axon gigantism: using axons several times larger in diameter
33            This demonstrates that polychaete gigantism was already a phenomenon in the Palaeozoic, so
34  (300 million years ago), a time when insect gigantism was widespread.
35                         Of the patients with gigantism who did not carry an Xq26.3 microduplication,

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。