(Q24682652)

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Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus

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Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus (English)

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31

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38

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36

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Richard Wooster

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Richard Wooster

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Sarah O'Meara

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Keiran Raine

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Sara Widaa

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Syd Barthorpe

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Gemma Buck

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Jennifer Varian

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Jennifer Varian

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Kristian Gray

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P. Andrew Futreal

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P Andrew Futreal

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Uma Mallya

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Douglas F. Easton

34

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Douglas F Easton

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Andrew Menzies

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Michael Stratton

39

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Michael R Stratton

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David Jones

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Patrick S. Tarpey

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Patrick S Tarpey

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29

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Jackie Boyle

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14

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Kelly Halliday

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Alexandra Small

22

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Alexandra Small

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Jonathon Hinton

16

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Jonathon Hinton

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4

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Calli Tofts

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author name string

F Lucy Raymond

1

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Adam Butler

7

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Claire Stevens

8

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Jennifer Cole

11

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Ed Dicks

12

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Katy Hills

15

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Janet Perry

19

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Rebecca Shepherd

21

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Jenny Moon

26

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Ying Luo

27

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Marie Shaw

28

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Bronwyn Kerr

30

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Oliver Quarrell

32

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Trevor Cole

33

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Charles E Schwartz

37

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language of work or name

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publication date

May 2007

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American Journal of Human Genetics

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80

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5

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982-7

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DHHC9 and GCP16 constitute a human protein fatty acyltransferase with specificity for H- and N-Ras

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Regulation of dendritic branching and filopodia formation in hippocampal neurons by specific acylated protein motifs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Germline KRAS mutations cause Noonan syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Germline mutations in HRAS proto-oncogene cause Costello syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

An acylation cycle regulates localization and activity of palmitoylated Ras isoforms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

7 April 2017

Spatio-temporal segregation of Ras signals: one ship, three anchors, many harbors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

28 September 2017

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

28 September 2017

Mutations in GDI1 are responsible for X-linked non-specific mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

28 September 2017

Revised diagnostic criteria for the Marfan syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

28 September 2017

Protein-truncating mutations in ASPM cause variable reduction in brain size

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

30 May 2018

Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

28 November 2018

Synaptic strength regulated by palmitate cycling on PSD-95.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852737

28 November 2018

Revised diagnostic criteria for the Marfan syndrome

1 reference

https://api.crossref.org/works/10.1086%2F513609

7 January 2021

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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