The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
The neurofibromatosis type 1 gene encodes a protein related to GAP
Abstract
cDNA walking and sequencing have extended the open reading frame for the neurofibromatosis type 1 gene (NF1). The new sequence now predicts 2485 amino acids of the NF1 peptide. A 360 residue region of the new peptide shows significant similarity to the known catalytic domains of both human and bovine GAP (GTPase activating protein). A much broader region, centered around this same 360 amino acid sequence, is strikingly similar to the yeast IRA1 product, which has a similar amino acid sequence and functional homology to mammalian GAP. This evidence suggests that NF1 encodes a cytoplasmic GAP-like protein that may be involved in the control of cell growth by interacting with proteins such as the RAS gene product. Mapping of the cDNA clones has confirmed that NF1 spans a t(1;17) translocation mutation and that three active genes lie within an intron of NF1, but in opposite orientation.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“KRAS proteins primarily bind to guanosine diphosphate (GDP) and are in an inactive conformation maintained by intrinsic guanosine triphosphate (GTP) hydrolytic activity.”
From Targeting KRAS mutant cancers: from druggable therapy to drug resistance (2022) · cites this paper as [9]
Citations
Cites
DNA sequencing with chain-terminating inhibitors
Sanger, F., Nicklen, S., & Coulson, A. R. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.12.5463 · Cited by 68,572
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
Feinberg, A. P., & Vogelstein, B. (1983) · Analytical Biochemistry · doi:10.1016/0003-2697(83)90418-9 · Cited by 24,512
A simple method for displaying the hydropathic character of a protein
Kyte, J., & Doolittle, R. F. (1982) · Journal of Molecular Biology · doi:10.1016/0022-2836(82)90515-0 · Cited by 22,927
A comprehensive set of sequence analysis programs for the VAX
Devereux, J., Haeberli, P. E., & Smithies, O. (1984) · Nucleic Acids Research · doi:10.1093/nar/12.1part1.387 · Cited by 14,222
Improved tools for biological sequence comparison.
Pearson, W. R., & Lipman, D. J. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.8.2444 · Cited by 11,227
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
(1984) · Analytical Biochemistry · doi:10.1016/0003-2697(84)90381-6 · Cited by 4,952
Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ
Benton, W. D., & Davis, R. W. (1977) · Science · doi:10.1126/science.322279 · Cited by 4,520
Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs
Kozak, M. (1984) · Nucleic Acids Research · doi:10.1093/nar/12.2.857 · Cited by 3,259
[5] Rapid and sensitive sequence comparison with FASTP and FASTA
Pearson, W. R. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)83007-v · Cited by 1,934
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
Wallace, M. R., Marchuk, D. A., Andersen, L. B., Letcher, R., Odeh, H. M., Saulino, A. M., Fountain, J. W., Brereton, A., Nicholson, J. M., Mitchell, A. L., et al. (1990) · Science · doi:10.1126/science.2134734 · Cited by 1,478
Research works printed but not linked: 1
- Stumpf, 1987, Neurofibromatosis, Arch. Neurol., 45, 575
Cited by
Sorted by citations
Items 701–800 of 1,000
Afshinnia, F., Vega-Warner, V., & Killen, P. (2013) · Clinical Kidney Journal · doi:10.1093/ckj/sft010 · Cited by 12
“The p21-ras protein binds to guanine nucleotides, possesses intrinsic GTPase activity and functions as an important regulator of cell growth [15, 16].”
BackgroundSakamoto, A., Oda, Y., Oshiro, Y., Tamiya, S., Iwamoto, Y., & Tsuneyoshi, M. (2001) · Human Pathology · doi:10.1053/hupa.2001.28954 · Cited by 12
Hernández-Imaz, E., Martín, Y., Conti, L. D., Melean, G., Valero, A., Baralle, M., & Hernández-Chico, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0141735 · Cited by 12
Chemical Carcinogenesis in Fishes
Rotchell, J. M., Miller, M., Hinton, D. E., Giulio, R. T. D., & Ostrander, G. K. (2008) · CRC Press eBooks · doi:10.1201/9780203647295.ch12 · Cited by 12
RNA Interference, Editing, and Modification
(2004) · Humana Press eBooks · doi:10.1385/1592597750 · Cited by 12
The Ras Signalling Pathway as a Target in Cancer Therapy
Graham, K., & Olson, M. F. (2007) · Springer eBooks · doi:10.1007/978-3-540-31209-3_8 · Cited by 12
Different functions of Smg GDP dissociation stimulator and mammalian counterpart of yeast Cdc25.
Nakanishi, H., Kaibuchi, K., Orita, S., Ueno, N., & Takai, Y. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)36577-8 · Cited by 12
Genetics of Neurofibromatosis 1-Associated Peripheral Nerve Sheath Tumors
Stephens, K. G. (2003) · Cancer Investigation · doi:10.1081/cnv-120025093 · Cited by 12
“One functional domain of neurofibromin has been defined, the GAP-related domain (GRD), so called because of its structural and functional homology to mammalian p120-GAP (GTPase activating protein) and yeast genes known to regulate the Ras pathway.([24,25]) The Ras-GAP proteins function as negative regulators of Ras by…”
BackgroundHorn, D., Robinson, P. N., Böddrich, A., Buske, A., Tinschert, S., & Nürnberg, P. (1996) · Electrophoresis · doi:10.1002/elps.1150171011 · Cited by 12
HOSOI, E., Yokogoshi, Y., Hosoi, E., Yokoi, K., Sano, T., & Saito, S. (1992) · Endocrinologia Japonica · doi:10.1507/endocrj1954.39.319 · Cited by 12
“Recently, in some hereditary tumors including retinoblastoma, Wilms' tumor, familial adenomatous polyposis, and neurofibromatosis, the discovery of a defect at a specific chromosomal loci resulted in the cloning of a gene which is inactivated during tumor development [1-4].”
BackgroundBiological actions of oncogenes
Smith, M. R., Matthews, N. T., Jones, K. A., & Kung, H. (1993) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(93)90050-n · Cited by 13
A deletion in the 5 ′-region of the neurofibromatosis type 1 (NF1) gene
Hoffmeyer, S., Assum, G., Kaufmann, D., Schwenk, K., & Krone, W. (1994) · Human Genetics · doi:10.1007/bf02272852 · Cited by 12
GTP binding proteins and growth factor signal transduction
Ives, H. E. (1991) · Cellular Signalling · doi:10.1016/0898-6568(91)90026-q · Cited by 12
Kaufmann, W. E., Yamagata, K., Andreasson, K. I., & Worley, P. F. (1994) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(94)90073-6 · Cited by 12
Recent Advances in the Development of Anticancer Drugs that Act against Signalling Pathways
Powis, G. (1994) · Tumori Journal · doi:10.1177/030089169408000201 · Cited by 12
Interactions between Ras and Rap signaling pathways during neurodevelopment in health and disease
Cherra, S. J., & Lamb, R. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1352731 · Cited by 11
Pathogenic noncoding variants in the neurofibromatosis and schwannomatosis predisposition genes
Perez‐Becerril, C., Evans, D. G., & Smith, M. J. (2021) · Human Mutation · doi:10.1002/humu.24261 · Cited by 13
“Regions of high homology with other members of GTPase activating protein (GAP) family exist between exons 21 and 27a (Y. Li et al., 1995; G. F. Xu et al., 1990).”
BackgroundHigh-grade primary diffuse leptomeningeal gliomatosis in a child with neurofibromatosis Type 1
King, J. A. J., HALLIDAY, W. C., & Drake, J. M. (2008) · Journal of Neurosurgery Pediatrics · doi:10.3171/ped.2008.2.12.402 · Cited by 11
Alanne, M. H., Siljamäki, E., Peltonen, S. A., Väänänen, K., Windle, J. J., Parada, L. F., Määttä, J. A., & Peltonen, J. T. K. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24088 · Cited by 12
“The NF1 gene product, neurofibromin, accelerates the hydrolysis of active Ras-GTP to inactive Ras-GDP thus regulating cell proliferation and differentiation [Xu et al., 1990].”
BackgroundAn Intracranial Leiomyosarcoma in a Child with Neurofibromatosis Type 1
Jhas, S., Henriques, L., Hawkins, C. E., Bouffet, É., & Rutka, J. T. (2009) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s031716710000785x · Cited by 11
Mori, S., Satoh, T., Koide, H., Nakafuku, M., Villafranca, E., & Kaziro, Y. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.48.28834 · Cited by 11
Neurofibromatosis: Novel and Recurrent Mutations in Turkish Patients
Terzi, Y. K., Balcı, S. O., Anlar, B., Aysun, S., & Ayter, Ş. (2007) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2007.07.005 · Cited by 11
Garicochea, B., Giorgi, R. R., Filho, V. O., Dorlhiac‐Llacer, P. E., & Bendit, I. (1998) · Leukemia Research · doi:10.1016/s0145-2126(98)00076-9 · Cited by 11
Radich, J. P., Kopecky, K. J., Appelbaum, F. R., Willman, C. L., & Collins, S. (1992) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.3109/10428199209053564 · Cited by 11
Tumor suppressor genes in molecular medicine
Hoppe‐Seyler, F., & Butz, K. (1994) · Journal of Molecular Medicine · doi:10.1007/bf00227456 · Cited by 11
“The NF1 gene product, neurofibromin, contains a high degree of amino acid homologies to GTPase-activating proteins [148].”
BackgroundStark, M., Assum, G., & Krone, W. (1995) · Human Genetics · doi:10.1007/bf00197423 · Cited by 11
“Krone ([Y:~) Abteilung Humangenetik, Universitit Ulm, Albert-Einstein-Allee 11, D-89070 Ulm, Germany shown to belong to the family of GTPase-activating proteins (GAP) on the basis of the structural and functional homology of a central domain ("GRD", GAP-related domain) to similar sequences within p l20GAP and other pr…”
BackgroundPollack, I. F., Bredel, M., & Erff, M. (1998) · Pediatric Neurosurgery · doi:10.1159/000028729 · Cited by 11
Candidate genes for multiple endocrine neoplasia type 1
Lagercrantz, J., Larsson, C., Grimmond, S. M., Skogseid, B. M., Gobl, A., Friedman, E., Carson, E., Phelan, C., Öberg, K., Nordenskjöld, M., et al. (1995) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.1995.tb00930.x · Cited by 11
Shen, Y.-C., Upadhyayula, R., Cevallos, S. A., Messick, R. J., Hsia, T., Leese, M. P., Jewett, D. M., Ferrer-Torres, D., Roth, T. M., Döhle, W., et al. (2015) · British Journal of Cancer · doi:10.1038/bjc.2015.345 · Cited by 10
“…type I (NF1) is an autosomal dominant disorder associated with loss-of-function mutations in the NF1 tumour suppressor gene that encodes the multi-functional protein Neurofibromin (Wallace et al, 1990; Xu et al, 1990; Roth et al, 2008a; Gottfried et al, 2010).”
BackgroundDoucet, E., Grychowska, K., Zajdel, P., Bockaert, J., Marin, P., & Bécamel, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810178 · Cited by 10
The RASopathies: Biology, genetics and therapeutic options
Longo, J. F., & Carroll, S. L. (2022) · Advances in cancer research · doi:10.1016/bs.acr.2021.07.007 · Cited by 10
Kallionpää, R. A., Johansson, E., Böckerman, P., Peltonen, J. T. K., & Peltonen, S. A. (2023) · European Journal of Human Genetics · doi:10.1038/s41431-023-01426-5 · Cited by 10
Raepple, D., von Lintig, F. C., Żemojtel, T., Duchniewicz, M., Jung, A., Lübbert, M., Boss, G. R., & Scheele, J. S. (2008) · Annals of Hematology · doi:10.1007/s00277-008-0593-6 · Cited by 10
“These include the Ras-GAP NF-1, which is mutatedintheautosomal dominantformofneurofibromatosis type 1 [ 16 , 17].”
BackgroundFatal malignant melanoma in a child with neurofibromatosis type 1
Binamer, Y., & Al‐Khenaizan, S. (2007) · International Journal of Dermatology · doi:10.1111/j.1365-4632.2007.03205.x · Cited by 10
Abnormalities of the p53 gene in juvenile myelomonocytic leukaemia
Miyauchi, J., Asada, M., Tsunematsu, Y., Kaneko, Y., Kojima, S., & Mizutani, S. (1999) · British Journal of Haematology · doi:10.1046/j.1365-2141.1999.01634.x · Cited by 10
“…tumour suppressor gene whose protein product has GTPase-activating protein activity and inactivates GTP-bound (active) form of ras family proteins (Xu et al, 1990; Boguski & McCormick, 1993), have been shown to be present in a substantial proportion of patients with JMML (Shannon et al, 1994;…”
BackgroundPark, K. C., Choi, H. O., Park, K. H., Kim, K. H., & Eun, H. C. (2000) · Journal of Human Genetics · doi:10.1007/s100380050016 · Cited by 10
“Neurofibromin can downregulate p21-Ras-GTP through its highly conserved, central GAP-related domain (GRD) (McCormick 1989).”
BackgroundSlam, K. D., Bohman, S., Sharma, R., & Chaudhuri, P. K. (2009) · The American Surgeon · doi:10.1177/000313480907500203 · Cited by 10
FAMILIAL NEUROGENIC TUMOR SYNDROMES
Kimmelman, A. C., & Liang, B. C. (2001) · Hematology/Oncology Clinics of North America · doi:10.1016/s0889-8588(05)70268-9 · Cited by 10
Analysis of the sequence and embryonic expression of chicken neurofibromin mRNA
Schafer, G. L., Ciment, G., Stocker, K. M., & Baizer, L. (1993) · Molecular and Chemical Neuropathology · doi:10.1007/bf03160119 · Cited by 10
“Analysis of the predicted amino acid sequence of the NF1 gene product (Ballester et al., 1990; Xu et al., 1990a ) reveals a 360 amino acid segment marked by a high degree of similarity to the ras-GTPase activator protein, or ras-GAP, which modulates ras-initiated signal transduction pathways (Trahey and McCormick, 198…”
BackgroundKim, J., & Powers, S. (1991) · Molecular and Cellular Biology · doi:10.1128/mcb.11.8.3894-3904.1991 · Cited by 10
“Nonredundant Ras GAPs may also exist in animal cells, in which two distinct proteins with GAP activity for p2lras have been discovered: cytoplasmic GAP and the NFI gene product (1, 24, 43, 47, 48).”
BackgroundTumour suppressors and the regulation of GTP-binding protein activity
Rey, I., & Hall, A. (1993) · Trends in Cell Biology · doi:10.1016/0962-8924(93)90149-u · Cited by 10
The clinical significance of antigen receptor gene rearrangements in lymphoid neoplasia
Sklar, J., & Longtine, J. (1992) · Cancer · doi:10.1002/1097-0142(19920915)70:4+ · Cited by 22
Molecular Genetics of von Recklinghausen Neurofibromatosis
Wallace, M. R., & Collins, F. S. (1991) · Springer eBooks · doi:10.1007/978-1-4684-5958-6_5 · Cited by 10
Epigenetics and survivorship in pediatric brain tumor patients
Bhattacharya, D., Pomeroy, S. L., Krummel, D. P., & Sengupta, S. (2020) · Journal of Neuro-Oncology · doi:10.1007/s11060-020-03535-3 · Cited by 9
Melanoma: Pathogenesis and Targeted Therapy
Fu, Y., Liu, J., Mo, Z., Wang, B., Deng, Y., & Jiang, Y. (2026) · MedComm · doi:10.1002/mco2.70566 · Cited by 11
“The NF1 protein functions as a negative regulator of RAS proteins via its GTPase activity [ 357 ].”
Bano, G., Mir, F., Beharry, N., Wilson, P., Hodgson, S. V., & Schey, S. (2012) · Intern J Endocrinol Metab · doi:10.5812/ijem.6898 · Cited by 9
Friedrich, R. E., & TUZCU, C. T. (2021) · In Vivo · doi:10.21873/invivo.12329 · Cited by 9
Lymphoproliferative malignancies in patients with neurofibromatosis 1
Bergqvist, C., Hémery, F., Jannic, A., Ferkal, S., & Wolkenstein, P. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-01856-8 · Cited by 9
“It is caused by mutations in the NF1 gene on chromosome 17 which encodes neurofibromin, a tumor suppressor protein [3, 4].”
BackgroundXu, J., Zhang, Y., Zhu, K., Li, J., Guan, Y., He, X., Jin, X., Bai, G., & Hu, L. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.991314 · Cited by 12
“The pathogenic mechanism of CPT is not clear yet and the deletion or inactivation of the NF1 gene is considered as an important cause (Xu et al., 1990; Basu et al., 1992; Cichowski and Jacks, 2001; Viskochil, 2002; Brekelmans et al., 2019).”
BackgroundHyaluronan in intra‐operative edema of NF1‐associated neurofibromas
Hagel, C., Behrens, T., Prehm, P., Schnabel, C., Glatzel, M., & Friedrich, R. E. (2011) · Neuropathology · doi:10.1111/j.1440-1789.2011.01276.x · Cited by 9
Oncogenes and tumor suppressor genes
Liu, E., & Weissman, B. E. (1993) · Cancer treatment and research · doi:10.1007/978-1-4615-3088-6_1 · Cited by 9
White matter is increased in the brains of adults with neurofibromatosis 1
Wang, S., Friedman, J. M., Suppa, P., Buchert, R., & Mautner, V. (2022) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-022-02273-1 · Cited by 9
Zhou, P., Chen, T., Fang, Y., Wang, H., Li, M., Ma, P., He, L., Li, Q., Liu, T., Yang, X., et al. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-1971-0 · Cited by 9
Ruptured Aneurysm of the Mammary Artery in a Patient With Neurofibromatosis Type I
Urso, S., Carballo, J., Greco, E., Pulitani, I., Álvarez, L., Juaristi, A., Larman, M., & Goiti, J. J. (2007) · Journal of Cardiac Surgery · doi:10.1111/j.1540-8191.2007.00396.x · Cited by 9
Tissue-specific alternative splicing of neurofibromatosis 1 (NF1) mRNA
Danglot, G., Teinturier, C., Duverger, A., & Bernheim, A. (1994) · Biomedicine & Pharmacotherapy · doi:10.1016/0753-3322(94)90053-1 · Cited by 9
Ogura, T., Adachi, J.-I., Nishikawa, R., Hirose, T., & Matsutani, M. (2004) · Pediatric Neurosurgery · doi:10.1159/000083744 · Cited by 9
Ikeda, H., Kawamoto, K., Paku, T., YOSHIDA, Y., Ito, T., & Ogasahara, K. (2008) · Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) · doi:10.3919/jjsa.69.1668 · Cited by 9
Genetic Predispositions and Childhood Cancer
Shannon, K. (1998) · Environmental Health Perspectives · doi:10.1289/ehp.98106801 · Cited by 9
The impact of germline mutations on targeted therapy
Smith, S. A., French, T., & Hollingsworth, S. J. (2013) · The Journal of Pathology · doi:10.1002/path.4273 · Cited by 9
“Of the latter, mutations in the Neurofibromin 1 (NF1 ) gene cause neurofibromatosis type 1, a tumour predisposition syndrome that largely affects the nervous system [77].”
BackgroundKaratzoglou, P., Karagiannidis, A., Kountouras, J., Christofiridis, C. V., Karavalaki, M., Zavos, C., Gavalas, E., Patsiaoura, K., & Vougiouklis, N. (2008) · PubMed · Cited by 9
Decayed, missing, and restored teeth in patients with Neurofibromatosis Type 1
Re, F., & Reul, A. (2018) · Journal of Clinical and Experimental Dentistry · doi:10.4317/jced.54561 · Cited by 9
Vessel and Mast Cell Densities in Sporadic and Syndrome-associated Peripheral Nerve Sheath Tumors.
Friedrich, R. E., Naber, U., Glatzel, M., & Hagel, C. (2015) · PubMed · Cited by 9
Recessive oncogenes: Current status
Gao, X., & Honn, K. V. (1995) · Pathology & Oncology Research · doi:10.1007/bf02893578 · Cited by 9
Symptomatic Tumors Affecting the Urinary Tract in Children With Neurofibromatosis
Barone, J. G., Massad, C. A., Parrott, T. S., Broecker, B. H., & Woodard, J. R. (1995) · The Journal of Urology · doi:10.1016/s0022-5347(01)66920-9 · Cited by 9
Perucho, M. (1994) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4612-0257-8_31 · Cited by 9
White, R. L. (1992) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(05)80321-1 · Cited by 9
Self-citationGómez, L., Barrios, C., Andris Kreicbergs, A., Zetterberg, A., ̃a, A. P., & Castresana, J. S. (1995) · Cancer Genetics and Cytogenetics · doi:10.1016/0165-4608(94)00267-f · Cited by 9
Transgenic mice as research tools in neurocarcinogenesis
Rovigatti, U., Afanasyeva, T., Brandner, S., Hainfellner, J. A., Kiess, M., Maddalena, A. S., Malin, G., Rülicke, T., Steinbach, J. P., Weissenberger, J., et al. (1998) · Journal of NeuroVirology · doi:10.3109/13550289809114516 · Cited by 9
“Neuro®bromatosis The Nf-1 gene, whose product is called neuro®bromin, was cloned in 1990 as the susceptibility gene for neuro®bromatosis 1 (Viskochil et al, 1990; Wallace et al, 1990) and subsequently discovered to encode a member of the GTPase activating proteins (GAP) (Xu et al, 1990).”
BackgroundHUGHES, D. A., & Yamamoto, M. P. (1993) · Elsevier eBooks · doi:10.1016/b978-0-12-429350-2.50010-3 · Cited by 9
Ras-Mediated Deregulation of Gene Expression and Contribution to Oncogenesis
Murphy, G. A., & Der, C. J. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-313-2_5 · Cited by 9
The Contribution of Oxidative Stress to NF1-Altered Tumors
Kuhn, E., Natacci, F., Corbo, M., Pisani, L., Ferrero, S., Bulfamante, G., & Gambini, D. (2023) · Antioxidants · doi:10.3390/antiox12081557 · Cited by 10
“Specifically, central exons between 20 and 27a encode the GAP-related domain that stimulates GTPase, which in turn hydrolyzes GTP bound to Ras, converting Ras-GTP to Ras-GDP, its inactivated form [59].”
BackgroundRichey, P. M., Funk, M. M., Sakamoto, F. H., Plotkin, S. R., Ly, I., Jordan, J. T., Muzikansky, A., Roberts, J., Farinelli, W. A., Levin, Y. S., et al. (2023) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2023.11.058 · Cited by 8
KRAS-targeted therapies in cancer: novel approaches and overcoming resistance
Tang, D., Kroemer, G., & Kang, R. (2025) · BMJ Oncology · doi:10.1136/bmjonc-2025-000946 · Cited by 12
“…Rac guanine nucleotide exchange factor 1 (SOS1), which promote the exchange of GDP for GTP, 16 17 and GTPase-activating proteins (GAPs), such as neurofi-bromin 1 (NF1), 18 19 which enhance the intrinsic GTPase activity of KRAS, facilitating GTP hydrolysis and returning KRAS to its inactive state.”
Ranalli, M., Boni, A., Caroleo, A. M., Baldo, G. D., Rinelli, M., Agolini, E., Rossi, S., Miele, E., Colafati, G. S., Boccuto, L., et al. (2021) · Diagnostics · doi:10.3390/diagnostics11040647 · Cited by 8
Characterization of Immune Cell Populations of Cutaneous Neurofibromas in Neurofibromatosis 1
Kallionpää, R. A., Peltonen, S. A., Le, K. M., Martikkala, E., Jääskeläinen, M., Fazeli, E., Riihilä, P., Haapaniemi, P., Rokka, A., Salmi, M., et al. (2023) · Laboratory Investigation · doi:10.1016/j.labinv.2023.100285 · Cited by 8
Qiao, G., Xuchun, J., Zhang, Y., & Chen, B. (2019) · Europe PMC (PubMed Central) · Cited by 8
Alterations in brain morphology by MRI in adults with neurofibromatosis 1
Wang, S., Mautner, V., Buchert, R., Flibotte, S., Suppa, P., Friedman, J. M., & Heran, M. K. S. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-02097-5 · Cited by 8
EAHP 2020 workshop proceedings, pediatric myeloid neoplasms
Leguit, R. J., Orazi, A., Kucine, N., Kvasnicka, H. M., Gianelli, U., Arber, D. A., Porwit‐MacDonald, A., & Ponzoni, M. (2022) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s00428-022-03375-8 · Cited by 8
Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines
Mitsudomi, T., Friedman, E., Gejman, P. V., McCormick, F. P., & Gazdar, A. F. (1994) · Human Genetics · doi:10.1007/bf00218908 · Cited by 8
Only in Congenial Soil: The Microenvironment in Brain Tumorigenesis
Rubin, J. B. (2008) · Brain Pathology · doi:10.1111/j.1750-3639.2008.00235.x · Cited by 8
Haploinsufficiency of the NF1 gene is associated with protection against diabetes
Kallionpää, R. A., Peltonen, S. A., Leppävirta, J., Pöyhönen, M., Auranen, K. J., Järveläinen, H., & Peltonen, J. T. K. (2020) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2020-107062 · Cited by 7
Yu, Z., Zhu, G., Liu, Y., Zhao, W., Yang, Y., Luo, Z., Fu, Y., Mei, H., & Hu, Z. (2022) · Human Genetics · doi:10.1007/s00439-021-02429-2 · Cited by 8
Uhlmann, E. J., & Gutmann, D. H. (2001) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:34:1:61 · Cited by 8
“Analysis of the predicted amino acid sequence reveals a 400 amino acid region of neurofibromin with sequence homology to GAP family of proteins (79).”
BackgroundHewitt, C., Wilson, P. J., McGlinn, E., Macfarlane, G. J., Papageorgiou, A., Woodwards, R. T. M., Sloan, P., Gollin, S. M., Paterson, I. C., Parkinson, K., et al. (2004) · Cancer Letters · doi:10.1016/j.canlet.2003.12.018 · Cited by 8
Mutation analysis of RASK and the ‘FLR exon’ of NF1 in sporadic ovarian carcinoma
Foulkes, W. D., Englefield, P., & Campbell, I. (1994) · European Journal of Cancer · doi:10.1016/0959-8049(94)90432-4 · Cited by 8
Familial cancer syndromes and genetic counseling
Tomlinson, G. E. (1997) · Cancer treatment and research · doi:10.1007/978-1-4615-5767-8_3 · Cited by 8
Jennings, S. B., Gnarra, J. R., Walther, M. M., Zbar, B., & Linehan, W. M. (1995) · Surgical Oncology Clinics of North America · doi:10.1016/s1055-3207(18)30449-6 · Cited by 8
Tumour suppressor genes and colorectal neoplasia
Koorey, D. J., & McCaughan, G. W. (1993) · Journal of Gastroenterology and Hepatology · doi:10.1111/j.1440-1746.1993.tb01511.x · Cited by 8
Molecular analysis of neurofibromatosis type 1 mutations
Xu, W., Yu, Q., Liu, L., Ponder, M. A., Wallace, M. R., Xu, G., & Ponder, B. A. J. (1992) · Human Mutation · doi:10.1002/humu.1380010604 · Cited by 8
“AE25 spans from nucleotides 2,5524,605, P5 spans from nucleotides 5,6257,308, and FB50 spans from nucleotides 6163,706 of the published NF1 cDNA sequence (Xu et al., 1990; Marchuk et al., 1991).”
Self-citationSuppression of ras oncogene-mediated transformation
Schäfer, R. (2006) · Springer eBooks · doi:10.1007/bfb0031031 · Cited by 8
Kundu, S., Rohokale, R., Lin, C., Chen, S., Biswas, S., & Guo, Z. (2024) · Journal of Lipid Research · doi:10.1016/j.jlr.2024.100570 · Cited by 7
Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion
Pizzuti, A., Bottillo, I., Inzana, F., Lanari, V., Buttarelli, F. R., Torrente, I., Giallonardo, A. T., Luca, A. D., & Dallapiccola, B. (2011) · Neurogenetics · doi:10.1007/s10048-011-0278-5 · Cited by 7
“codes for neurofibromin [1, 2], an important negative regulator of the cellular Ras signaling pathway [3–6].”
BackgroundTian, H., Chen, Z., Jie, G., Wang, Z., Yan, H., Wu, S.-P., Zhang, S., Lu, D., Zhang, X., & Wu, Y.-L. L. C. (2022) · Cancer Medicine · doi:10.1002/cam4.4925 · Cited by 7
Predicting IHC staining classes of NF1 using features in the hematoxylin channel
Zhang, W., Koh, M. Y., Sirohi, D., Ying, J., Brintz, B. J., & Knudsen, B. S. (2023) · Journal of Pathology Informatics · doi:10.1016/j.jpi.2023.100196 · Cited by 7
Han, J., Qu, L., Li, Y., Luo, J., Cao, J., & Zhao, W. (2012) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.35417 · Cited by 7
“Approximately, one-half of cases of NF1 are diagnosed without a known family history and are thought to represent new mutations [Xu et al., 1990; Cichowski and Jacks, 2001; Ars et al., 2003; Ferner et al., 2007].”
BackgroundShorvon, S. D., Andermann, F., & Guerrini, R. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511921001.016 · Cited by 7
Wolkenstein, P. (2001) · médecine/sciences · doi:10.1051/medsci/200117111158 · Cited by 7
“Ces protéines (GAP) augmentent le taux d’hydrolyse de GTP et agissent donc comme modulateur négatif de Ras [48, 49].”
BackgroundSong, K., Lu, H., Jin, L., Wang, K., Guo, W., Zheng, H., Li, K., He, C., You, T., Fu, Y., et al. (2020) · FEBS Journal · doi:10.1111/febs.15306 · Cited by 7
Genetics and Epigenetics of Pancreatic Neuroendocrine Tumors and Pulmonary Carcinoids
Dreijerink, K. M. A., Derks, J. L., Cataldo, I., Scarpa, A., Valk, G. D., & Speel, E. M. (2015) · Frontiers of hormone research · doi:10.1159/000382138 · Cited by 7
Malignant peripheral nerve sheath tumor
Stawicki, S. P., Shen, Y., Hon, H., Papadimos, T. J., & Schrag, S. (2015) · International Journal of Academic Medicine · doi:10.4103/2455-5568.172704 · Cited by 7
Metadata
- Authors
- Xu, G., O'Connell, P., Viskochil, D., Cawthon, R., Robertson, M., Culver, M., Dunn, D., Stevens, J., Gesteland, R., White, R., & Weiss, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- University of Utah (US)
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1990-08
- Volume
- 62
- Issue
- 3
- Pages
- 599-608
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2159096148
- Cited by
- 1,095
- References
- 42
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 19 · 2023: 19 · 2022: 22 · 2021: 22 · 2020: 22 · 2019: 18 · 2018: 22 · 2017: 17 · 2016: 19 · 2015: 21 · 2014: 24 · 2013: 24 · 2012: 45
- FWCI
- 70.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- U.S. Department of Energy
- Topics
- Health Sciences › Medicine › Clinical Neurology › Neurofibromatosis and Schwannoma Cases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- neurofibromatosis type 1, NF1 gene, GTPase-activating protein, Ras, open reading frames, cDNA cloning, cell growth regulation, protein homology
- MeSH terms
- Amino Acid Sequence, Animals, Base Sequence, Cattle, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 17, Cloning, Molecular, Genes, Humans, Information Systems, Molecular Sequence Data, Neurofibromatosis 1, Proteins, Sequence Homology, Nucleic Acid, Translocation, Genetic, Oligonucleotide Probes, Gene Library, Polymerase Chain Reaction, GTPase-Activating Proteins, ras GTPase-Activating Proteins, Neurofibromin 1
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review