(Q28241532)

21 June 2017

title

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (English)

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21 June 2017

27

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21 June 2017

Lynne M Bird

10

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Hakon Hakonarson

23

object named as

Hakon Hakonarson

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21 June 2017

25

Leslie G Biesecker

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21 June 2017

22

Lynn B Jorde

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21 June 2017

12

John M Opitz

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21 June 2017

2

Kai Wang

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21 June 2017

17

Reid Robison

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21 June 2017

28

Gholson J Lyon

1 reference

21 June 2017

1

Alan F Rope

1 reference

21 June 2017

4

Jinchuan Xing

1 reference

21 June 2017

6

Jeffrey J Swensen

1 reference

21 June 2017

8

Barry Moore

1 reference

21 June 2017

9

Chad D Huff

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21 June 2017

13

Cathy A Stevens

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21 June 2017

15

Christa Schank

1 reference

21 June 2017

16

Heidi Deborah Fain

1 reference

21 June 2017

18

Brian Dalley

1 reference

21 June 2017

21

Theodore J Pysher

1 reference

21 June 2017

24

Johan R Lillehaug

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21 June 2017

3

Rune Evjenth

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21 June 2017

26

Mark Yandell

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21 June 2017

Jennifer J Johnston

5

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21 June 2017

W Evan Johnson

7

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21 June 2017

John C Carey

11

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21 June 2017

Tao Jiang

14

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21 June 2017

Steven Chin

19

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21 June 2017

Sarah T South

20

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21 June 2017

language of work or name

English

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publication date

23 June 2011

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American Journal of Human Genetics

21 June 2017

published in

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21 June 2017

volume

89

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21 June 2017

issue

1

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21 June 2017

page(s)

28-43

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Proteome-derived peptide libraries allow detailed analysis of the substrate specificities of N(alpha)-acetyltransferases and point to hNaa10p as the post-translational actin N(alpha)-acetyltransferase

21 June 2017

cites work

1 reference

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Depletion of the human Nα-terminal acetyltransferase A induces p53-dependent apoptosis and p53-independent growth inhibition

20 March 2017

1 reference

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N-α-acetyltransferase 10 protein suppresses cancer cell metastasis by binding PIX proteins and inhibiting Cdc42/Rac1 activity

20 March 2017

1 reference

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A map of human genome variation from population-scale sequencing

20 March 2017

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20 March 2017

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Drosophila variable nurse cells encodes arrest defective 1 (ARD1), the catalytic subunit of the major N‐terminal acetyltransferase complex

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

20 March 2017

1 reference

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Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

20 March 2017

1 reference

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20 March 2017

1 reference

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hNaa10p contributes to tumorigenesis by facilitating DNMT1-mediated tumor suppressor gene silencing

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Exome sequencing identifies the cause of a mendelian disorder

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Database resources of the National Center for Biotechnology Information

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

The GNUMAP algorithm: unbiased probabilistic mapping of oligonucleotides from next-generation sequencing

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Human Naa50p (Nat5/San) displays both protein N alpha- and N epsilon-acetyltransferase activity

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Human arrest defective 1 acetylates and activates beta-catenin, promoting lung cancer cell proliferation

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Characterization of the native and fibrillar conformation of the human Nalpha-acetyltransferase ARD1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Identification and characterization of the human ARD1-NATH protein acetyltransferase complex

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Genetic manipulation indicates that ARD1 is an essential N(alpha)-acetyltransferase in Trypanosoma brucei

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Conformational parameters for amino acids in helical, beta-sheet, and random coil regions calculated from proteins

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Identification and characterization of genes and mutants for an N-terminal acetyltransferase from yeast.

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

A standard variation file format for human genome sequences

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Exome sequencing of a multigenerational human pedigree

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

SIFT: Predicting amino acid changes that affect protein function

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

A high-resolution recombination map of the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

A probabilistic disease-gene finder for personal genomes.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Maximum-likelihood estimation of recent shared ancestry (ERSA).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

N-terminal acetylation of cellular proteins creates specific degradation signals

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Application of reverse-phase HPLC to quantify oligopeptide acetylation eliminates interference from unspecific acetyl CoA hydrolysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

A synopsis of eukaryotic Nalpha-terminal acetyltransferases: nomenclature, subunits and substrates

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Proteomics analyses reveal the evolutionary conservation and divergence of N-terminal acetyltransferases from yeast and humans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

From the rarest to the most common: insights from progeroid syndromes into skin cancer and aging.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135802

Designation of the TARP syndrome and linkage to Xp11.23-q13.3 without samples from affected patients

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21700266

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2011.05.017

1 reference

OpenCitations bibliographic resource ID

21 June 2017

2703748

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2703748

1 reference