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English
Syndromes run together in the RAS pathway
scientific article published on 01 March 2006
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
title
Syndromes run together in the RAS pathway
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
publication date
1 March 2006
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
volume
38
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
issue
3
1 reference
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Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
page(s)
267
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/ng0306-267
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Genetic disorders in portraits
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0306-267
retrieved
7 January 2021
based on heuristic
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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0306-267
retrieved
7 January 2021
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Germline mutations in HRAS proto-oncogene cause Costello syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2FNG0306-267
retrieved
7 January 2021
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Molecular neurobiology of human cognition.
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0306-267
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NF1 gene mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0306-267
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gain-of-function/Noonan syndrome SHP-2/Ptpn11 mutants enhance calcium oscillations and impair NFAT signaling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0306-267
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0306-267
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
PubMed publication ID
16501550
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16501550
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16501550%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 January 2020
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