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Page 1
Did you mean cynrg (1 results)?
ZNF384-Related Fusion Genes in Acute Lymphoblastic Leukemia.
Zhu L, Bai W, Cheng Q, Fang J. Zhu L, et al. Cancer Control. 2023 Jan-Dec;30:10732748231182787. doi: 10.1177/10732748231182787. Cancer Control. 2023. PMID: 37306722 Free PMC article. Review.
These include E1A-binding protein P300 (EP300), CREB-binding protein (CREBBP), transcription factor 3 (TCF3), TATA-box binding protein associated factor 15 (TAF15), Ewing sarcoma breakpoint region 1 gene (EWSR1), AT-rich interactive domain-containing protein 1B (ARID1B), SWI/SNF …
These include E1A-binding protein P300 (EP300), CREB-binding protein (CREBBP), transcription factor 3 (TCF3), TATA-box binding protein assoc …
Variation in the management of isolated craniosynostosis: a survey of the Synostosis Research Group.
Kestle JRW, Lee A, Anderson RCE, Gociman B, Patel KB, Smyth MD, Birgfeld C, Pollack IF, Goldstein JA, Tamber M, Imahiyerobo T, Siddiqi FA; Synostosis Research Group. Kestle JRW, et al. J Neurosurg Pediatr. 2018 Dec 1;22(6):627-631. doi: 10.3171/2018.7.PEDS18132. Epub 2018 Sep 14. J Neurosurg Pediatr. 2018. PMID: 30215587
OBJECTIVEThe authors created a collaborative network, the Synostosis Research Group (SynRG), to facilitate multicenter clinical research on craniosynostosis. To identify common and differing practice patterns within the network, they assessed the SynRG surgeons' man …
OBJECTIVEThe authors created a collaborative network, the Synostosis Research Group (SynRG), to facilitate multicenter clinical resea …
Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia.
Ayaz A, Uzunhan TA, Aydin K. Ayaz A, et al. Brain Dev. 2022 May;44(5):329-335. doi: 10.1016/j.braindev.2022.01.002. Epub 2022 Jan 25. Brain Dev. 2022. PMID: 35090779
RESULTS: The p.Leu1202Pro variant in the SYNRG gene in the 1st and 2nd cases, and the p.Gly533* variant in the 3rd case were homozygous. ...It may be important to evaluate SYNRG gene variants in patients with hereditary spastic paraplegia whose etiology has not been …
RESULTS: The p.Leu1202Pro variant in the SYNRG gene in the 1st and 2nd cases, and the p.Gly533* variant in the 3rd case were homozygo …
Evaluation of 3,606 renal cell tumors for TFE3 rearrangements and TFEB alterations via fluorescence in situ hybridization, next generation sequencing, and GPNMB immunohistochemistry.
Whaley RD, Sill DR, Tekin B, McCarthy MR, Cheville JC, Ebare K, Stanton ML, Reynolds JP, Raghunathan A, Herrera Hernandez LP, Jimenez RE, Sharma V, Boorjian SA, Leibovich BC, Hofich CD, Alvand S, Pujari GP, Kipp BR, Ketterling RP, Geiersbach KB, Greipp PT, Sukov WR, Halling KC, Gupta S. Whaley RD, et al. Hum Pathol. 2025 May;159:105797. doi: 10.1016/j.humpath.2025.105797. Epub 2025 May 15. Hum Pathol. 2025. PMID: 40381702
TFE3-RCC fusion partners included RBM10, NONO, ASPSCR1, FUBP1, SFPQ, MAPK1IP1L, and PRCC. TFEB-rearranged RCC fusion partners SYNRG and BYSL were identified. Diffuse GPNMB expression was seen in 92% of TFE3-RCC (24/26; median H-score 275), 100% of TFEB-rearranged RCC (19/1 …
TFE3-RCC fusion partners included RBM10, NONO, ASPSCR1, FUBP1, SFPQ, MAPK1IP1L, and PRCC. TFEB-rearranged RCC fusion partners SYNRG a …
A multi-institutional survey on calvarial vault remodeling techniques for sagittal synostosis and outcomes analysis for patients treated at 12 months and older.
Chi D, Gibson E, Chiang SN, Lee K, Naidoo SD, Lee A, Birgfeld C, Pollack IF, Goldstein J, Golinko M, Bonfield CM, Siddiqi FA, Kestle JRW, Smyth MD, Patel KB; Synostosis Research Group (SynRG). Chi D, et al. J Neurosurg Pediatr. 2022 Aug 19;30(5):490-498. doi: 10.3171/2022.7.PEDS22139. Print 2022 Nov 1. J Neurosurg Pediatr. 2022. PMID: 35986730
This study aimed to assess the effect of increasing age on open surgical technique selection and patient outcomes using the multi-institutional Synostosis Research Group (SynRG) collaboration. METHODS: Surgeons in SynRG were surveyed for key influences on their pref …
This study aimed to assess the effect of increasing age on open surgical technique selection and patient outcomes using the multi-institutio …
Management of sagittal synostosis in the Synostosis Research Group: baseline data and early outcomes.
Baker CM, Ravindra VM, Gociman B, Siddiqi FA, Goldstein JA, Smyth MD, Lee A, Anderson RCE, Patel KB, Birgfeld C, Pollack IF, Imahiyerobo T, Kestle JRW; Synostosis Research Group. Baker CM, et al. Neurosurg Focus. 2021 Apr;50(4):E3. doi: 10.3171/2021.1.FOCUS201029. Neurosurg Focus. 2021. PMID: 33794498
In 2017, the Synostosis Research Group (SynRG), a multicenter collaborative network, was formed to study craniosynostosis. Here, the authors report their early experience with treating sagittal synostosis in the network. ...Data extracted from the prospectively maintained …
In 2017, the Synostosis Research Group (SynRG), a multicenter collaborative network, was formed to study craniosynostosis. Here, the …
The aftiphilin/p200/gamma-synergin complex.
Hirst J, Borner GH, Harbour M, Robinson MS. Hirst J, et al. Mol Biol Cell. 2005 May;16(5):2554-65. doi: 10.1091/mbc.e04-12-1077. Epub 2005 Mar 9. Mol Biol Cell. 2005. PMID: 15758025 Free PMC article.
Identification of a Risk Allele at SLC41A3 and a Protective Allele HLA-DPB1*02:01 Associated with Sarcopenia in Japanese.
Furutani M, Kimura T, Fukunaga K, Suganuma M, Takemura M, Matsui Y, Satake S, Nakano Y, Mushiroda T, Niida S, Ozaki K, Hosoyama T, Shigemizu D. Furutani M, et al. Gerontology. 2025;71(5):376-387. doi: 10.1159/000545298. Epub 2025 Mar 18. Gerontology. 2025. PMID: 40552851
RESULTS: Rare variant analysis identified five rare coding variants of genes - SLC41A3, SYNRG, CLUAP1, CCHCR1, and ALDH2 - expressed in skeletal muscle. Of these, a deleterious frameshift deletion in SLC41A3 was associated with the pathogenesis of sarcopenia (p = 0.0012, o …
RESULTS: Rare variant analysis identified five rare coding variants of genes - SLC41A3, SYNRG, CLUAP1, CCHCR1, and ALDH2 - expressed …
Expert Recommendations for Neurodevelopmental Screening in Children with Craniosynostosis: A Consensus Report from the Craniosynostosis Research Neurodevelopmental Working Group (SynRG).
Baraya N, Thibodaux L, Martin A, Stone C, Strahle J, Patel K, Chapman L. Baraya N, et al. Cleft Palate Craniofac J. 2025 May 14:10556656251339879. doi: 10.1177/10556656251339879. Online ahead of print. Cleft Palate Craniofac J. 2025. PMID: 40368325
The proposed protocol was then presented to multidisciplinary members of the SynRG research group, including surgeons and craniofacial specialists, to refine recommendations.SettingThe protocol is intended for implementation in multidisciplinary craniosynostosis clinics at …
The proposed protocol was then presented to multidisciplinary members of the SynRG research group, including surgeons and craniofacia …
ZNF384-fusion proteins have high affinity for the transcriptional coactivator EP300 and aberrant transcriptional activities.
Yamamoto H, Hayakawa F, Yasuda T, Odaira K, Minamikawa Y, Tange N, Hirano D, Kojima Y, Morishita T, Tsuzuki S, Naoe T, Kiyoi H. Yamamoto H, et al. FEBS Lett. 2019 Aug;593(16):2151-2161. doi: 10.1002/1873-3468.13506. Epub 2019 Jul 10. FEBS Lett. 2019. PMID: 31234226 Free article.
We selected SALL4 and ID2 as potential Z-fusion-specific transcriptional targets that might lead to the differentiation disorder of Z-fusion-positive ALL. The introduction of EP300-ZNF384 and SYNRG-ZNF384 induced the expression of these genes. Z-fusion proteins exhibited s …
We selected SALL4 and ID2 as potential Z-fusion-specific transcriptional targets that might lead to the differentiation disorder of Z-fusion …
30 results