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NF1: a prevalent cause of tumorigenesis in human cancers?
scientific article published on 01 February 1993
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
title
NF1: a prevalent cause of tumorigenesis in human cancers?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
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Seizinger BR
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1
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
publication date
1 February 1993
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
volume
3
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
page(s)
97-99
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0293-97
0 references
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Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17
1 reference
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7 January 2021
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Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene
1 reference
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7 January 2021
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A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
1 reference
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Crossref
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retrieved
7 January 2021
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Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0293-97
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7 January 2021
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Neurofibromatosis type 1 gene mutations in neuroblastoma
1 reference
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Crossref
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7 January 2021
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Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Von Recklinghausen neurofibromatosis
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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The neurofibromatosis type 1 gene encodes a protein related to GAP
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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The catalytic domain of the neurofibromatosis type 1 gene product stimulates ras GTPase and complements ira mutants of S. cerevisiae
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Sequence homology shared by neurofibromatosis type-1 gene and IRA-1 and IRA-2 negative regulators of the RAS cyclic AMP pathway.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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The GAP-related domain of the neurofibromatosis type 1 gene product interacts with ras p21
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic mutations in the neurofibromatosis 1 gene in human tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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Mutation and cancer: statistical study of retinoblastoma
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
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A review of astrocytoma in childhood
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNG0293-97
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential regulation of rasGAP and neurofibromatosis gene product activities
1 reference
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Crossref
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retrieved
7 January 2021
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Recent progress toward understanding the molecular biology of von Recklinghausen neurofibromatosis
1 reference
stated in
Crossref
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retrieved
7 January 2021
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Promotion of microtubule assembly in vitro by taxol
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Crossref
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7 January 2021
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Identifiers
DOI
10.1038/NG0293-97
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
PubMed ID
7848376
1 reference
stated in
Europe PubMed Central
PubMed ID
7848376
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7848376%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 October 2019
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