ライフサイエンスコーパス: HMG-box protein

1 rate to regulate cellular localization of an HMG box protein.

2 sequence-dependent binding by a nonspecific HMG-box protein.

3 r that is a fungal ortholog of the hSRY/SOX9 HMG box proteins.

4 are highly effective, preferred, ligands for HMG-box proteins.

5 of the properties of (non-sequence specific) HMG-box proteins.

6 were similar to each other and to other NSS HMG-box proteins.

7 nd Tip60 interact directly via the ATXN1 and HMG-box protein 1 (AXH) domain of ATXN1.

8 This review will focus on the HMG-box protein 1 (HBP1) transcriptional repressor and i

9 ataxin-1 share a conserved AXH (ataxin-1 and HMG-box protein 1) domain, which is essential for both p

10 In contrast, HBP1 (HMG-box protein-1), a novel retinoblastoma protein-bindi

11 We found that Sry HMG box protein 9-positive (Sox9(+)) epithelial cell adh

12 A mitochondrial HMG box protein, Abf2p, is needed for maintenance of mtD

13 strate the applicability of this approach to HMG-box proteins and contrast the results obtained for n

14 as compared to the lower affinities of other HMG box proteins; and (3) ribosomal RNA transcription in

15 SOX (SRY type HMG box) proteins are transcription factors that are pre

16 evelopment in animals (homeodomain proteins, HMG-box proteins) are also central to the control of sex

17 Here, we show that the HMG-box protein Capicua (Cic) restricts cell growth in D

18 ms a bipartite transcription factor with the HMG-box protein Drosophila Tcf (dTcf) and activates expr

19 We discovered that the interaction of the HMG-box protein HMG20B with LSD1 was also disrupted by L

20 e structure occurred when Spt16-Pob3 and the HMG box protein Nhp6 were both present, but Nhp6 alone a

21 Here we show that SOX1, an HMG-box protein related to SRY, is one of the earliest t

22 e Y chromosome)-related high mobility group (HMG) box) proteins require the calcium-binding protein c

23 a nucleus-encoded, high-mobility-group-box (HMG-box) protein that regulates transcription of the mit

24 d be relevant in the hierarchy of binding of HMG-box proteins to DNA distortions in vivo, where both

25 We show here that expression of the HMG box protein TOX is sufficient to induce changes in c

26 tive selection caused by loss of the nuclear HMG box protein TOX.

27 ranscriptional regulation by the DNA-binding HMG-box protein TOX which remodels more than 400 genomic

28 The annotated thymocyte selection-associated HMG-box protein (TOX) coding sequence is predicted to pr

29 pecific (SS) and non-sequence-specific (NSS) HMG box proteins were studied with various DNA recogniti

30 ryos, we identified a novel function for the HMG box protein XSox17 beta.