(Q30157309)

18 August 2017

Expression, purification, crystallization and preliminary X-ray crystallographic analysis of the SH3 domain of human AHI1 (English)

1 reference

18 August 2017

0 references

Zhuliang Shi

1

1 reference

18 August 2017

Ning Liang

2

1 reference

18 August 2017

Wei Xu

3

1 reference

18 August 2017

Kuai Li

4

1 reference

18 August 2017

Guoqing Sheng

5

1 reference

18 August 2017

Jinsong Liu

6

1 reference

18 August 2017

Aimin Xu

7

1 reference

18 August 2017

Xiao Jiang Li

8

1 reference

18 August 2017

Donghai Wu

9

1 reference

18 August 2017

21 March 2009

1 reference

Acta Crystallographica Section F: Structural Biology Communications

18 August 2017

1 reference

18 August 2017

65

1 reference

18 August 2017

Pt 4

1 reference

18 August 2017

361-363

1 reference

Huntingtin-associated protein 1 interacts with Ahi1 to regulate cerebellar and brainstem development in mice

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

The CCP4 suite: programs for protein crystallography

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

Ahi-1, a novel gene encoding a modular protein with WD40-repeat and SH3 domains, is targeted by the Ahi-1 and Mis-2 provirus integrations

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

SH3 domains: complexity in moderation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

High-resolution crystal structures of tyrosine kinase SH3 domains complexed with proline-rich peptides

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

Lck unique domain influences Lck specificity and biological function

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

Solvent content of protein crystals

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

Joubert syndrome (and related disorders) (OMIM 213300).

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664760

10.1107/S174430910900774X

26 November 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference

18 August 2017

PubMed publication ID

19342780

1 reference