(Q36489640)

14 August 2017

Structural basis of an embryonically lethal single Ala --> Thr mutation in the vnd/NK-2 homeodomain (English)

1 reference

14 August 2017

Xiang B

1

1 reference

14 August 2017

Weiler S

series ordinal

2

1 reference

14 August 2017

Nirenberg M

series ordinal

3

1 reference

14 August 2017

Ferretti JA

series ordinal

4

1 reference

14 August 2017

language of work or name

English

0 references

publication date

1 June 1998

1 reference

Proceedings of the National Academy of Sciences of the United States of America

14 August 2017

1 reference

14 August 2017

95

1 reference

14 August 2017

13

1 reference

14 August 2017

7412-7416

1 reference

The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Point Mutations Within and Outside the Homeodomain Identify Sequences Required for proboscipedia Homeotic Function in Drosophila

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Interactions of the vnd/NK-2 homeodomain with DNA by nuclear magnetic resonance spectroscopy: basis of binding specificity

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

A single-point mutation in HCF causes temperature-sensitive cell-cycle arrest and disrupts VP16 function.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Mutation of HOXA13 in hand-foot-genital syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

NMRPipe: a multidimensional spectral processing system based on UNIX pipes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Amino acid type determination in the sequential assignment procedure of uniformly 13C/15N-enriched proteins.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

The ventral nervous system defective gene controls proneural gene expression at two distinct steps during neuroblast formation in Drosophila.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

The Three-dimensional Solution Structure of the NK-2 Homeodomain fromDrosophila

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

vnd, a gene required for early neurogenesis of Drosophila, encodes a homeodomain protein

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

The NK-2 homeobox gene and the early development of the central nervous system of Drosophila.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Crystal structure of the MATa1/MAT alpha 2 homeodomain heterodimer bound to DNA

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Genetic and developmental analysis of the locus vnd in Drosophila melanogaster

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Drosophila NK-homeobox genes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Crystal structure of an engrailed homeodomain-DNA complex at 2.8 A resolution: a framework for understanding homeodomain-DNA interactions

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Protein--DNA contacts in the structure of a homeodomain--DNA complex determined by nuclear magnetic resonance spectroscopy in solution

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Crystal structure of a MAT alpha 2 homeodomain-operator complex suggests a general model for homeodomain-DNA interactions

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

A homeodomain point mutation of the Drosophila proboscipedia protein provokes eye loss independently of homeotic function.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

The structure of the Antennapedia homeodomain determined by NMR spectroscopy in solution: comparison with prokaryotic repressors.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Defective neuroblast commitment in mutants of the achaete-scute complex and adjacent genes of D. melanogaster

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22634

Dorsal-ventral patterning genes restrict NK-2 homeobox gene expression to the ventral half of the central nervous system of Drosophila embryos.

28 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.13.7412

Elongation of helix III of the NK-2 homeodomain upon binding to DNA: a secondary structure study by NMR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.13.7412

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.13.7412

Site-directed mutations in the vnd/NK-2 homeodomain. Basis of variations in structure and sequence-specific DNA binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.13.7412

Correlating backbone amide and side chain resonances in larger proteins by multiple relayed triple resonance NMR

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.13.7412

Increased Resolution and Improved Spectral Quality in Four-Dimensional 13C/13C-Separated HMQC-NOESY-HMQC Spectra Using Pulsed Field Gradients

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.13.7412

Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.13.7412

21 January 2018

Identifiers

DOI

10.1073/PNAS.95.13.7412

1 reference

14 August 2017

0 references

1 reference

14 August 2017

PubMed publication ID

9636163

1 reference