The DOI matches its Crossref record; 89 of the 89 references it cites were found in a registry or an index; none of the 62 sources its claims cite is checked for support yet.
Rac GTPases in Human Diseases
Open accessAbstract
Rho GTPases are members of the Ras superfamily of GTPases that regulate a wide variety of cellular functions. While Rho GTPase pathways have been implicated in various pathological conditions in humans, to date coding mutations in only the hematopoietic specific GTPase,RAC2, have been found to cause a human disease, a severe phagocytic immunodeficiency characterized by life-threatening infections in infancy. Interestingly, the phenotype was predicted by a mouse knock-out of RAC2 and resembles leukocyte adhesion deficiency (LAD). Here we review Rho GTPases with a specific focus on Rac GTPases. In particular, we discuss a new understanding of the unique and overlapping roles of Rac2 in blood cells that has developed since the generation of mice deficient in Rac1, Rac2 and Rac3 proteins. We propose that Rac2 mutations leading to disease be termed LAD type IV.
Overview
CoChat Summary
Written by AI from the paper’s full text.
TL;DR
This review summarizes the roles of Rho family GTPases, focusing on the Rac subfamily, in blood cell biology and human disease. It argues that the two reported cases of dominant-negative RAC2 mutation causing severe phagocytic immunodeficiency—resembling leukocyte adhesion deficiency—should be termed LAD type IV.
Key findings
- To date, coding mutations in only one Rho GTPase, the hematopoietic-specific RAC2, have been found to cause human disease; mutations in the first intron of RHOH have been implicated in B cell malignancies.
- Two patients with a c.169G>A mutation predicting p.Asp57Asn (D57N) in RAC2 presented as newborns with infection around the umbilical stump, neutrophilia/leukocytosis, absent pus, and recurrent life-threatening bacterial infections; both required allogeneic hematopoietic stem cell transplantation.
- Patient cells recapitulated the Rac2−/− mouse phenotype: defects in chemotaxis, migration, F-actin formation, and selective NADPH oxidase defects (a CGD feature), with normal CD11b/CD18 expression ruling out LAD type I.
- The second patient, identified by newborn screening for SCID, had complete absence of TREC (0–4/µL vs. mean 225/µL in normal newborns; cutoff <25/µL) but only mild T cell lymphopenia (1434/µL) with increased CD45RO expression.
- The authors propose the term LAD type IV for this disease.
Methods
- Narrative review of Rho/Rac GTPase biology, integrating in vitro mutant studies, gene-targeted mouse models (Rac1, Rac2, Rac3 knockouts and conditional/double knockouts), and clinical data from two human RAC2 mutation cases.
- Includes a summary table (Table 1) comparing laboratory abnormalities across Case 1, Case 2, and the Rac2−/− mouse (neutrophil count, exudate formation, NADPH oxidase responses, adhesion, chemotaxis, F-actin formation, phagocytosis, degranulation).
- No primary experimental data are generated; the second patient's data are cited as unpublished (courtesy of J. Routes, J. Verbsky et al.).
Limitations
- The paper notes that dominant-negative mutant studies suffer from non-specific effects and expression-level dependence, and that cell-line work may not reflect primary cells; the second human case relies partly on unpublished data.
- The authors state that why TREC are disproportionately low in the mild lymphopenia case "remains unclear," and that the human lymphocyte phenotype is less severe than in doubly deficient mice, possibly reflecting null vs. dominant-negative differences.
- Evident from the text: only two human RAC2 cases are described, and the LAD type IV nomenclature is a proposal rather than an established classification.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
40 Sources not found · 16 Own result · 13 Own interpretation · 1 Own method · 1 No basis given
In the paper
“observed abnormal myeloid development in vitro after transduction of HSC/P with the DN D57NRac2 mutant, which most likely inhibits Rac3 in addition to Rac1 and Rac2 [76].”
What the sources say
- Not matchedcites [76]
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
boostedstates a cause- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Not matched
A result the paper states — it cites no source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The clinical presentation of both patients was charac- terized by defects in neutrophiladhesion and migration.”
plainstates an association- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“The findings from this case have now been corroborated by a second case, which came to attention in the course of universal newborn screen- ing in Wisconsin for severe combined immunodeficien- cy (SCID) [69] and unpublished data (courtesy of J. Routes, J. Verbsky et. al.).”
What the sources say
- Not matchedcites [69]
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plainstates an association- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Not matched
A result the paper states — it cites no source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Many of these findings were also seen in the second patient.”
plainstates an associationSingle case- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper states — it cites no source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Both children were found to have a c.169G>A mu- tation that results in a predicted protein change of p.Asp57Asn (D57N).”
plainstates a cause- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Probably not a substantial claim. 11
- It may state two separate claims as one. 25
Create a free account to see these claims.
Create a free account to see these assumptions.
30 more claims
Create a free account to see all 71 claims and every source verdict.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
“The Rho proteins can be divided into 6 families based on sequence homology, protein domains and function.”
“These include Rac,RhoA, Cdc42,TC10 and TCL, Rnd, the Rho BTB subset and the Miro subfamily.”
Citations
Cites
Rho GTPases and the Actin Cytoskeleton
Hall, A. (1998) · Science · doi:10.1126/science.279.5350.509 · Cited by 6,138
Wnt signalling in stem cells and cancer
Reya, T., & Clevers, H. (2005) · Nature · doi:10.1038/nature03319 · Cited by 3,666
Rho GTPases and signaling networksPreprint
Aelst, L. V., & D’Souza‐Schorey, C. (1997) · Genes & Development · doi:10.1101/gad.11.18.2295 · Cited by 2,358
A role for Wnt signalling in self-renewal of haematopoietic stem cells
Reya, T., Duncan, A. W., Ailles, L., Domen, J., Scherer, D. C., Willert, K., Hintz, L., Nusse, R., & Weissman, I. L. (2003) · Nature · doi:10.1038/nature01593 · Cited by 2,159
Changes in thymic function with age and during the treatment of HIV infection
Douek, D. C., McFarland, R. D., Keiser, P. H., Gage, E. A., Massey, J. M., Haynes, B. F., Polis, M. A., Haase, A. T., Feinberg, M. B., Sullivan#, J. L., et al. (1998) · Nature · doi:10.1038/25374 · Cited by 1,893
PROTEIN PRENYLATION: Molecular Mechanisms and Functional Consequences
Zhang, F. L., & Casey, P. J. (1996) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.65.070196.001325 · Cited by 1,743
Sahai, E., & Marshall, C. J. (2002) · Nature Reviews Cancer · doi:10.1038/nrc725 · Cited by 1,261
Identification and characterization of leukemia stem cells in murine MLL-AF9 acute myeloid leukemia
Somervaille, T. C. P., & Cleary, M. L. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.08.020 · Cited by 582
Roberts, A. W., Kim, C., Zhen, L., Lowe, J. B., Kapur, R., Petryniak, B., Spaetti, A., Pollock, J. D., Borneo, J. B., Bradford, G. B., et al. (1999) · Immunity · doi:10.1016/s1074-7613(00)80019-9 · Cited by 556
Self-citationFleming, H. E., Janzen, V., Celso, C. L., Guo, J., Leahy, K. M., Kronenberg, H. M., & Scadden, D. T. (2008) · Cell stem cell · doi:10.1016/j.stem.2008.01.003 · Cited by 529
A Role for Cdc42 in Macrophage Chemotaxis
Allen, W. E., Zicha, D., Ridley, A. J., & Jones, G. E. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.5.1147 · Cited by 528
Regulation of Phagocyte Oxygen Radical Production by the GTP-Binding Protein Rac 2
Knaus, U. G., Heyworth, P. G., Evans, T., Curnutte, J. T., & Bokoch, G. M. (1991) · Science · doi:10.1126/science.1660188 · Cited by 525
Activation of the nuclear factor-kappaB by Rho, CDC42, and Rac-1 proteins
Perona, R., Montaner, S., Saniger, L., Sánchez-Pérez, I., Bravo, R., & Lacal, J. C. (1997) · Genes & Development · doi:10.1101/gad.11.4.463 · Cited by 519
Hematopoietic Cell Regulation by Rac1 and Rac2 Guanosine Triphosphatases
Gu, Y., Filippi, M.-D., Cancelas, J. A., Siefring, J. E., Williams, E. P., Jasti, A. C., Harris, C. E., Lee, A. W., Prabhakar, R., Atkinson, S. J., et al. (2003) · Science · doi:10.1126/science.1088485 · Cited by 510
Self-citationRac1 Activation Controls Nuclear Localization of β-catenin during Canonical Wnt Signaling
Wu, X., Tu, X., Joeng, K. S., Hilton, M. J., Williams, D. A., & Long, F. (2008) · Cell · doi:10.1016/j.cell.2008.01.052 · Cited by 501
Self-citationRho GTPases have diverse effects on the organization of the actin filament system
Aspenström, P., Fransson, Å., & Saras, J. (2004) · Biochemical Journal · doi:10.1042/bj20031041 · Cited by 437
Requirements for both Rac1 and Cdc42 in membrane ruffling and phagocytosis in leukocytes
Cox, D., Chang, P., Zhang, Q., Reddy, P. G., Bokoch, G. M., & Greenberg, S. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.186.9.1487 · Cited by 436
Rho, Rac and Cdc42 regulate actin organization and cell adhesion in macrophages
Allen, W. E., Jones, G. E., Pollard, J. W., & Ridley, A. J. (1997) · Journal of Cell Science · doi:10.1242/jcs.110.6.707 · Cited by 409
Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation
Ambruso, D. R., Knall, C., Abell, A. N., Panepinto, J., Kurkchubasche, A., Thurman, G., Gonzalez-Aller, C., Hiester, A., deBoer, M., Harbeck, R. J., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.080074897 · Cited by 407
Rho family proteins and Ras transformation: the RHOad less traveled gets congested
Zohn, I. M., Campbell, S. L., Khosravi-Far, R., Rossman, K. L., & Der, C. J. (1998) · Oncogene · doi:10.1038/sj.onc.1202181 · Cited by 352
Dbl family guanine nucleotide exchange factors
Zheng, Y. (2001) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(01)01973-9 · Cited by 339
Rac1 Deletion in Mouse Neutrophils Has Selective Effects on Neutrophil Functions
Glogauer, M., Marchal, C. C., Zhu, F., Worku, A. D., Clausen, B. E., Foerster, I., Marks, P. W., Downey, G. P., Dinauer, M. C., & Kwiatkowski, D. J. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.11.5652 · Cited by 315
Microenvironment Determines Lineage Fate in a Human Model of MLL-AF9 Leukemia
Wei, J., Wunderlich, M., Fox, C., Alvarez, S., Cigudosa, J. C., Wilhelm, J. S., Zheng, Y., Cancelas, J. A., Gu, Y., Jansen, M., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.04.020 · Cited by 284
Rho GTPases in transformation and metastasis
Jaffe, A. B., & Hall, A. (2002) · Advances in cancer research · doi:10.1016/s0065-230x(02)84003-9 · Cited by 279
Rac GTPases differentially integrate signals regulating hematopoietic stem cell localization
Cancelas, J. A., Lee, A. W., Prabhakar, R., Stringer, K. F., Zheng, Y., & Williams, D. A. (2005) · Nature Medicine · doi:10.1038/nm1274 · Cited by 278
Self-citationAbo, A., Boyhan, A., West, I., Thrasher, A. J., & Segal, A. W. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)41846-7 · Cited by 267
Mira, J., Planat‐Benard, V., Groffen, J., Sanders, L. C., & Knaus, U. G. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.1.185 · Cited by 244
Foster, R., Hu, K.-Q., Lu, Y., Nolan, K. M., Thissen, J., & Settleman, J. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.6.2689 · Cited by 240
Critical roles for Rac1 and Rac2 GTPases in B cell development and signaling
Walmsley, M. J., Ooi, S. K. T., Reynolds, L. F., Smith, S. H., Ruf, S., Mathiot, A., Vanes, L., Williams, D. A., Cancro, M. P., & Tybulewicz, V. L. J. (2003) · Science · doi:10.1126/science.1089709 · Cited by 238
Self-citationEnucleation of cultured mouse fetal erythroblasts requires Rac GTPases and mDia2
Ji, P., Jayapal, S. R., & Lodish, H. F. (2008) · Nature Cell Biology · doi:10.1038/ncb1693 · Cited by 235
Resh, M. D. (1996) · Cellular Signalling · doi:10.1016/s0898-6568(96)00088-5 · Cited by 217
Rho family members: activators of MAP kinase cascades
Vojtek, A. B., & Cooper, J. A. (1995) · Cell · doi:10.1016/0092-8674(95)90023-3 · Cited by 216
Statewide newborn screening for severe T-cell lymphopenia
Routes, J. M. (2009) · JAMA · doi:10.1001/jama.2009.1806 · Cited by 203
Roles of the Rac1 and Rac3 GTPases in human tumor cell invasion
Chan, A. Y., Coniglio, S. J., Chuang, Y.-Y., Michaelson, D., Knaus, U. G., Philips, M. R., & Symons, M. (2005) · Oncogene · doi:10.1038/sj.onc.1208909 · Cited by 202
Rac and Cdc42 GTPases control hematopoietic stem cell shape, adhesion, migration, and mobilization
Yang, F.-C., Atkinson, S. J., Gu, Y., Borneo, J. B., Roberts, A. W., Zheng, Y., Pennington, J., & Williams, D. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.101546898 · Cited by 201
Self-citationRho GTPases in hematopoiesis and hemopathies
Mulloy, J. C., Cancelas, J. A., Filippi, M., Kalfa, T. A., Guo, F., & Zheng, Y. (2009) · Blood · doi:10.1182/blood-2009-09-198127 · Cited by 172
Signaling from Ras to Rac and beyond: not just a matter of GEFs
Scita, G., Tenca, P., Frittoli, E., Tocchetti, A., Innocenti, M., Giardina, G., & Di Fiore, P. P. (2000) · The EMBO Journal · doi:10.1093/emboj/19.11.2393 · Cited by 170
Arana, E., Vehlow, A., Harwood, N. E., Vigorito, E., Henderson, R., Turner, M., Tybulewicz, V. L. J., & Batista, F. D. (2008) · Immunity · doi:10.1016/j.immuni.2007.12.003 · Cited by 156
Kim, C., & Dinauer, M. C. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.2.1223 · Cited by 151
Self-citationEnzymology and biology of CaaX protein prenylation.
Fu, H., & Casey, P. J. (1999) · PubMed · Cited by 151
Thomas, E. K., Cancelas, J. A., Chae, H.-D., Cox, A. D., Keller, P. J., Perrotti, D., Neviani, P., Druker, B. J., Setchell, K. D. R., Zheng, Y., et al. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.10.015 · Cited by 147
Self-citationPopulation-based newborn screening for severe combined immunodeficiency: Steps toward implementation
Puck, J. M. (2007) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2007.08.043 · Cited by 138
山内, 明., Kim, C., Li, S., Marchal, C. C., Towe, J., Atkinson, S. J., & Dinauer, M. C. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.10.5971 · Cited by 137
Self-citationRac2 is critical for neutrophil primary granule exocytosis
Abdel-Latif, D., Steward, M., Macdonald, D. L., Francis, G. A., Dinauer, M. C., & Lacy, P. (2004) · Blood · doi:10.1182/blood-2003-07-2624 · Cited by 132
Baugher, P. J., Krishnamoorthy, L., Price, J. E., & Dharmawardhane, S. F. (2005) · Breast Cancer Research · doi:10.1186/bcr1329 · Cited by 131
Yang, F.-C., Kapur, R., King, A. J., Tao, W., Kim, C., Borneo, J., Breese, R., Marshall, M., Dinauer, M. C., & Williams, D. A. (2000) · Immunity · doi:10.1016/s1074-7613(00)80207-1 · Cited by 126
Self-citationCroker, B. A., Tarlinton, D. M., Cluse, L. A., Tuxen, A. J., Light, A., Yang, F., Williams, D. A., & Roberts, A. W. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.7.3376 · Cited by 125
Self-citationPrimary granule exocytosis in human neutrophils is regulated by Rac-dependent actin remodeling
Mitchell, T., Lo, A. N., Logan, M. R., Lacy, P., & Eitzen, G. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00239.2008 · Cited by 122
Cooperation between Syk and Rac1 Leads to Synergistic JNK Activation in T Lymphocytes
Jacinto, E., Werlen, G., & Karin, M. (1998) · Immunity · doi:10.1016/s1074-7613(00)80456-2 · Cited by 121
Generation and Characterization of Rac3 Knockout Mice
Corbetta, S., Gualdoni, S., Albertinazzi, C., Paris, S., Croci, L., Consalez, G. G., & de Curtis, I. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.13.5763-5776.2005 · Cited by 116
Rac GTPases regulate the morphology and deformability of the erythrocyte cytoskeleton
Kalfa, T. A., Pushkaran, S., Mohandas, N., Hartwig, J. H., Fowler, V. M., Johnson, J. F., Joiner, C. H., Williams, D. A., & Zheng, Y. (2006) · Blood · doi:10.1182/blood-2006-03-005942 · Cited by 113
Self-citationFilippi, M.-D., Harris, C. E., Meller, J., Gu, Y., Zheng, Y., & Williams, D. A. (2004) · Nature Immunology · doi:10.1038/ni1081 · Cited by 110
Self-citationLi, S., Yamauchi, A., Marchal, C. C., Molitoris, J. K., Quilliam, L. A., & Dinauer, M. C. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.9.5043 · Cited by 109
Rac GTPase isoforms Rac1 and Rac2 play a redundant and crucial role in T-cell development
Guo, F., Cancelas, J. A., Hildeman, D., Williams, D. A., & Zheng, Y. (2008) · Blood · doi:10.1182/blood-2008-01-132068 · Cited by 100
Self-citationGu, Y., Jia, B., Yang, F.-C., D'Souza, M., Harris, C. E., Derrow, C. W., Zheng, Y., & Williams, D. A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010445200 · Cited by 100
Self-citationKawashima, T., Bao, Y. C., Nomura, Y., Moon, Y., Tonozuka, Y., Minoshima, Y., Hatori, T., Tsuchiya, A., Kiyono, M., Nosaka, T., et al. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200604073 · Cited by 100
Self-citationPrenylated Rab Acceptor Protein Is a Receptor for Prenylated Small GTPases
Figueroa‐Romero, C., Taylor, J., & Vojtek, A. B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101763200 · Cited by 97
Chae, H.-D., Lee, K. E., Williams, D. A., & Gu, Y. (2008) · Blood · doi:10.1182/blood-2007-06-093237 · Cited by 81
Self-citationAkbar, H., Kim, J. J. Y. B., Funk, K. M., Cancelas, J. A., Shang, X., Chen, L., Johnson, J. F., Williams, D. A., & Zheng, Y. (2007) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2007.02646.x · Cited by 79
Self-citationReview of Mammalian DNA Repair and Translational Implications
Hansen, W. K., & Kelley, M. R. (2000) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)38861-5 · Cited by 78
Protein prenylation: from discovery to prospects for cancer treatment
Gelb, M. H., Scholten, J. D., & Sebolt, J. S. (1998) · Current Opinion in Chemical Biology · doi:10.1016/s1367-5931(98)80034-3 · Cited by 77
Rho GTPase Rac1 is critical for neutrophil migration into the lung
Filippi, M., Szczur, K., Harris, C. E., & Berclaz, P. (2006) · Blood · doi:10.1182/blood-2006-04-017731 · Cited by 77
Sinensky, M. S. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s1388-1981(00)00149-9 · Cited by 74
Gringhuis, S. I., de Leij, L. F. M. H., Coffer, P. J., & Vellenga, E. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.3.1725 · Cited by 72
Comeau, A. M., Hale, J. E., Pai, S., Bonilla, F. A., Notarangelo, L. D., Pasternack, M. S., Meissner, H. C., Cooper, E. R., DeMaria, A., Sahai, I., et al. (2010) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-010-9103-9 · Cited by 70
Self-citationFritz, G. (2000) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(00)00045-5 · Cited by 67
Rac GTPases play critical roles in early T-cell development
Dumont, C., Corsoni-Tadrzak, A., Ruf, S., de Boer, J., Williams, A., Turner, M., Kioussis, D., & Tybulewicz, V. L. J. (2009) · Blood · doi:10.1182/blood-2008-09-181180 · Cited by 66
Small GTPase RhoD suppresses cell migration and cytokinesis
Tsubakimoto, K., Matsumoto, K., Abe, H., Ishii, J., Amano, M., Kaibuchi, K., & Endo, T. (1999) · Oncogene · doi:10.1038/sj.onc.1202604 · Cited by 64
Kalfa, T. A., Pushkaran, S., Zhang, X., Johnson, J. F., Pan, D., Daria, D., Geiger, H., Cancelas, J. A., Williams, D. A., & Zheng, Y. (2010) · Haematologica · doi:10.3324/haematol.2009.006239 · Cited by 63
Self-citationL-Selectin Regulates Actin Polymerisation via Activation of the Small G-Protein Rac2
Brenner, B., Gulbins, E., Busch, G. L., Koppenhoefer, U., Lang, F. J. W., & Linderkamp, O. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6191 · Cited by 63
Gu, Y., Byrne, M. C., Paranavitana, N. C., Aronow, B. J., Siefring, J. E., D'Souza, M., Horton, H. F., Quilliam, L. A., & Williams, D. A. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.21.7645-7657.2002 · Cited by 60
Self-citationLorès, P., Morin, L., Luna, R., & Gacon, G. (1997) · Oncogene · doi:10.1038/sj.onc.1201378 · Cited by 59
Carstanjen, D., Yamauchi, A., Koornneef, A., Zang, H., Filippi, M.-D., Harris, C., Towe, J., Atkinson, S., Zheng, Y., Dinauer, M. C., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.8.4613 · Cited by 56
Self-citationHuman neutrophils coordinate chemotaxis by differential activation of Rac1 and Rac2
Zhang, H., Sun, C., Glogauer, M., & Bokoch, G. M. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900849 · Cited by 50
Suzuki, D., Yamada, A., Amano, T., Yasuhara, R., Kimura, A., Sakahara, M., Tsumaki, N., Takeda, S., Tamura, M., Nakamura, M., et al. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.09.014 · Cited by 50
Generation of rac3 Null Mutant Mice: Role of Rac3 in Bcr/Abl-Caused Lymphoblastic Leukemia
Cho, Y. J., Zhang, B., Kaartinen, V., Haataja, L., de Curtis, I., Groffen, J., & Heisterkamp, N. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.13.5777-5785.2005 · Cited by 50
Clinical features of a human Rac2 mutation: a complex neutrophil dysfunction disease
Kurkchubasche, A. G., Panepinto, J. A., Tracy, T. F., Thurman, G. W., & Ambruso, D. R. (2001) · The Journal of Pediatrics · doi:10.1067/mpd.2001.114718 · Cited by 49
Rac Is Involved in Early TCR Signaling
Arrieumerlou, C., Randriamampita, C., Bismuth, G., & Trautmann, A. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.6.3182 · Cited by 46
Reibel, L., Dorseuil, O., Stancou, R., Bertoglio, J., & Gacon, G. (1991) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(91)91585-z · Cited by 43
Tao, W., Filippi, M., Bailey, J. R., Atkinson, S. J., Connors, B. A., Evan, A. P., & Williams, D. A. (2002) · Blood · doi:10.1182/blood.v100.5.1679.h81702001679_1679_1688 · Cited by 41
Self-citationRho GTPases in hematopoietic stem cell functions
Cancelas, J. A., & Williams, D. A. (2009) · Current Opinion in Hematology · doi:10.1097/moh.0b013e32832c4b80 · Cited by 40
Self-citationRegulation of inflammation by Rac2 in immune complex-mediated acute lung injury
Dooley, J., Abdel-Latif, D., Laurent, C. D. S., Puttagunta, L., Befus, A. D., & Lacy, P. (2009) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.90471.2008 · Cited by 33
Rac guanosine triphosphatases represent a potential target in AML
Müller, L. U. W., Schore, R. J., Zheng, Y., Thomas, E. K., Kim, M.-O., Cancelas, J. A., Gu, Y., & Williams, D. A. (2008) · Leukemia · doi:10.1038/leu.2008.196 · Cited by 30
Self-citationMorris, C. M., Haataja, L., Mcdonald, M., Gough, S. M., Markie, D., Groffen, J., & Heisterkamp, N. (2000) · Cytogenetic and Genome Research · doi:10.1159/000015583 · Cited by 22
Rac3-Mediated Transformation Requires Multiple Effector Pathways
Keller, P. J., Gable, C. M., Wing, M. R., & Cox, A. D. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-3116 · Cited by 15
Gomez, J. C., Šoltýs, J., Okano, K., Dinauer, M. C., & Doerschuk, C. M. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.071059 · Cited by 14
Roberts, P. J., Mollapour, E., Watts, M., & Linch, D. C. (1999) · Blood · doi:10.1182/blood.v94.4.1261 · Cited by 9
Rac GTPases are involved in development, survival and homeostasis of T cells
Sato, Y., Oda, H., Patrick, M. S., Baba, Y., Rus’D, A. A., Azuma, Y., Abe, T., Shirai, M., & Suzuki, H. (2009) · Immunology Letters · doi:10.1016/j.imlet.2009.03.014 · Cited by 7
(2000) · PubMed
Self-citation
Cited by
Practice parameter for the diagnosis and management of primary immunodeficiency
Bonilla, F. A., Khan, D. A., Ballas, Z. K., Chinen, J., Frank, M. M., Hsu, J. T., Keller, M. D., Kobrynski, L. J., Komarow, H. D., Mazer, B. D., et al. (2015) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.04.049 · Cited by 832
Hall, A. (2012) · Biochemical Society Transactions · doi:10.1042/bst20120103 · Cited by 579
Characterization of EHop-016, Novel Small Molecule Inhibitor of Rac GTPase
Montalvo-Ortiz, B. L., Castillo-Pichardo, L., Hernández, E., Humphries-Bickley, T., De La Mota-Peynado, A., Cubano, L. A., Vlaar, C. P., & Dharmawardhane, S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.334524 · Cited by 213
Nieborowska-Skorska, M., Kopinski, P. K., Ray, R., Hoser, G., Ngaba, D., Flis, S., Cramer, K., Reddy, M. M., Koptyra, M., Penserga, T., et al. (2012) · Blood · doi:10.1182/blood-2011-10-385658 · Cited by 177
Self-citationDirect multiplex imaging and optogenetics of Rho GTPases enabled by near-infrared FRET
Shcherbakova, D. M., Cammer, N. C., Huisman, T. M., Verkhusha, V. V., & Hodgson, L. (2018) · Nature Chemical Biology · doi:10.1038/s41589-018-0044-1 · Cited by 154
Metadata
- Authors
- Pai, S.-Y., Kim, C., & Williams, D. A.
- Affiliations
- Boston Children's Hospital (US)
- Inha University (KR)
- Corresponding author
- Williams, David A.
- Venue
- Disease Markers
- Publisher
- Wiley
- Published
- 2010
- Volume
- 29
- Issue
- 3-4
- Pages
- 177-187
- ISSN
- 0278-0240 (ISSN-L)
- 1875-8630
- PMC
- PMC3835286
- OpenAlex
- W4239395424
- Cited by
- 85
- References
- 89
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 5 · 2023: 3 · 2022: 2 · 2021: 3 · 2020: 6 · 2019: 7 · 2018: 7 · 2017: 5 · 2016: 8 · 2015: 9 · 2014: 6 · 2013: 8 · 2012: 6
- FWCI
- 1.91
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Disease Markers (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- PubMed
- Funders
- National Institutes of Health (DK062757, CA113969, AI083907, A080244)
- Children’s Hospital Boston Translational Investigator Service (SYP) (DK062757, CA113969, AI083907, A080244)
- Health Care Medical Technology R&D Projects (DK062757, CA113969, AI083907, A080244)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
- Keywords
- Rac GTPase, Rho GTPases, Rac2, Rac1, RAC3, hematopoietic cells, Ras superfamily
- MeSH terms
- Animals, Hematopoietic System, Humans, Infant, Mutation, Opportunistic Infections, Phagocytes, Signal Transduction, Mice, Knockout, Leukocyte-Adhesion Deficiency Syndrome, Protein Isoforms, rac GTP-Binding Proteins, Mice, Genetic Association Studies
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.
A language model drew the claims from the paper on 2026-11-12, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-11-12 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
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