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For: Hanson D, Murray PG, Black GC, Clayton PE. The genetics of 3-M syndrome: unravelling a potential new regulatory growth pathway. Horm Res Paediatr. 2011;76:369-378. [PMID: 22156540 DOI: 10.1159/000334392] [Cited by in Crossref: 24] [Cited by in F6Publishing: 22] [Article Influence: 2.2] [Reference Citation Analysis]
Number Citing Articles
1 Clayton PE, Hanson D, Magee L, Murray PG, Saunders E, Abu-Amero SN, Moore GE, Black GC. Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination. Clin Endocrinol (Oxf). 2012;77:335-342. [PMID: 22624670 DOI: 10.1111/j.1365-2265.2012.04428.x] [Cited by in Crossref: 35] [Cited by in F6Publishing: 32] [Article Influence: 3.9] [Reference Citation Analysis]
2 Holder-Espinasse M, Irving M, Cormier-Daire V. Clinical utility gene card for: 3-M syndrome - update 2013. Eur J Hum Genet 2014;22. [PMID: 23900270 DOI: 10.1038/ejhg.2013.156] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 0.7] [Reference Citation Analysis]
3 Yan J, Yan F, Li Z, Sinnott B, Cappell KM, Yu Y, Mo J, Duncan JA, Chen X, Cormier-Daire V, Whitehurst AW, Xiong Y. The 3M complex maintains microtubule and genome integrity. Mol Cell 2014;54:791-804. [PMID: 24793695 DOI: 10.1016/j.molcel.2014.03.047] [Cited by in Crossref: 47] [Cited by in F6Publishing: 41] [Article Influence: 5.9] [Reference Citation Analysis]
4 Kaneko-Ishino T, Ishino F. The role of genes domesticated from LTR retrotransposons and retroviruses in mammals. Front Microbiol 2012;3:262. [PMID: 22866050 DOI: 10.3389/fmicb.2012.00262] [Cited by in Crossref: 50] [Cited by in F6Publishing: 45] [Article Influence: 5.0] [Reference Citation Analysis]
5 Pulavarti SV, Huang YJ, Pederson K, Acton TB, Xiao R, Everett JK, Prestegard JH, Montelione GT, Szyperski T. Solution NMR structures of immunoglobulin-like domains 7 and 12 from obscurin-like protein 1 contribute to the structural coverage of the Human Cancer Protein Interaction Network. J Struct Funct Genomics 2014;15:209-14. [PMID: 24989974 DOI: 10.1007/s10969-014-9185-y] [Reference Citation Analysis]
6 Hanson D, Stevens A, Murray PG, Black GC, Clayton PE. Identifying biological pathways that underlie primordial short stature using network analysis. J Mol Endocrinol 2014;52:333-44. [PMID: 24711643 DOI: 10.1530/JME-14-0029] [Cited by in Crossref: 23] [Cited by in F6Publishing: 15] [Article Influence: 2.9] [Reference Citation Analysis]
7 Wei M, Zhao X, Liu M, Huang Z, Xiao Y, Niu M, Shao Y, Kleiman L. Inhibition of HIV-1 assembly by coiled-coil domain containing protein 8 in human cells. Sci Rep 2015;5:14724. [PMID: 26423533 DOI: 10.1038/srep14724] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
8 Dauber A, Stoler J, Hechter E, Safer J, Hirschhorn JN. Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorder. J Pediatr 2013;162:202-4.e1. [PMID: 22974575 DOI: 10.1016/j.jpeds.2012.07.055] [Cited by in Crossref: 19] [Cited by in F6Publishing: 21] [Article Influence: 1.9] [Reference Citation Analysis]
9 Guo L, Feng Z, Jin X, Yin S, Zhang M, Gao Y, Zhang B, Wang H, Liu L. A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon. Clin Chim Acta 2020;507:23-30. [PMID: 32278698 DOI: 10.1016/j.cca.2020.04.008] [Reference Citation Analysis]
10 Blondelle J, Marrocco V, Clark M, Desmond P, Myers S, Nguyen J, Wright M, Bremner S, Pierantozzi E, Ward S, Estève E, Sorrentino V, Ghassemian M, Lange S. Murine obscurin and Obsl1 have functionally redundant roles in sarcolemmal integrity, sarcoplasmic reticulum organization, and muscle metabolism. Commun Biol 2019;2:178. [PMID: 31098411 DOI: 10.1038/s42003-019-0405-7] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
11 Jiang X, Jia X, Sun J, Qi C, Lu L, Wang Y, Zhang L, Wei M. Overexpressed coiled-coil domain containing protein 8 (CCDC8) mediates newly synthesized HIV-1 Gag lysosomal degradation. Sci Rep 2020;10:11416. [PMID: 32651437 DOI: 10.1038/s41598-020-68341-3] [Reference Citation Analysis]
12 Kong C, Samovski D, Srikanth P, Wainszelbaum MJ, Charron AJ, Liu J, Lange JJ, Chen PI, Pan ZQ, Su X, Stahl PD. Ubiquitination and degradation of the hominoid-specific oncoprotein TBC1D3 is mediated by CUL7 E3 ligase. PLoS One 2012;7:e46485. [PMID: 23029530 DOI: 10.1371/journal.pone.0046485] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 1.7] [Reference Citation Analysis]
13 Storr HL, Chatterjee S, Metherell LA, Foley C, Rosenfeld RG, Backeljauw PF, Dauber A, Savage MO, Hwa V. Nonclassical GH Insensitivity: Characterization of Mild Abnormalities of GH Action. Endocr Rev 2019;40:476-505. [PMID: 30265312 DOI: 10.1210/er.2018-00146] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 5.7] [Reference Citation Analysis]
14 Lee IK, Lim HH, Kim YM. The Effect of Combined Growth Hormone and a Gonadotropin-Releasing Hormone Agonist Therapy on Height in Korean 3-M Syndrome Siblings. Yonsei Med J 2020;61:981-5. [PMID: 33107243 DOI: 10.3349/ymj.2020.61.11.981] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Randall JM, Millard F, Kurzrock R. Molecular aberrations, targeted therapy, and renal cell carcinoma: current state-of-the-art. Cancer Metastasis Rev 2014;33:1109-24. [PMID: 25365943 DOI: 10.1007/s10555-014-9533-1] [Cited by in Crossref: 51] [Cited by in F6Publishing: 47] [Article Influence: 7.3] [Reference Citation Analysis]
16 Hu L, Wang X, Jin T, Han Y, Liu J, Jiang M, Yan S, Fu X, An B, Huang S. Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing. J Clin Lab Anal 2020;34:e23265. [PMID: 32141654 DOI: 10.1002/jcla.23265] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
17 Shaikh S, Shettigar SKG, Kumar S, Kantharia S, Kurva J, Cherian S. Novel mutation in Cul7 gene in a family diagnosed with 3M syndrome. J Genet 2019;98. [DOI: 10.1007/s12041-019-1057-6] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Takatani T, Shiohama T, Takatani R, Shimojo N. A novel CUL7 mutation in a Japanese patient with 3M syndrome. Hum Genome Var 2018;5:30. [PMID: 30374406 DOI: 10.1038/s41439-018-0029-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
19 Tüysüz B, Alp Ünkar Z, Turan H, Gezdirici A, Uludağ Alkaya D, Kasap B, Yeşil G, Vural M, Ercan O. Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants. Eur J Med Genet 2021;64:104346. [PMID: 34597859 DOI: 10.1016/j.ejmg.2021.104346] [Reference Citation Analysis]
20 Shapiro L, Chatterjee S, Ramadan DG, Davies KM, Savage MO, Metherell LA, Storr HL. Whole-exome sequencing gives additional benefits compared to candidate gene sequencing in the molecular diagnosis of children with growth hormone or IGF-1 insensitivity. Eur J Endocrinol 2017;177:485-501. [PMID: 28870985 DOI: 10.1530/EJE-17-0453] [Cited by in Crossref: 18] [Cited by in F6Publishing: 7] [Article Influence: 3.6] [Reference Citation Analysis]
21 Jiang GY, Zhang XP, Zhang Y, Xu HT, Wang L, Li QC, Wang EH. Coiled-coil domain-containing protein 8 inhibits the invasiveness and migration of non-small cell lung cancer cells. Hum Pathol 2016;56:64-73. [PMID: 27342910 DOI: 10.1016/j.humpath.2016.06.001] [Cited by in Crossref: 12] [Cited by in F6Publishing: 15] [Article Influence: 2.0] [Reference Citation Analysis]
22 Marshall CR, Farrell SA, Cushing D, Paton T, Stockley TL, Stavropoulos DJ, Ray PN, Szego M, Lau L, Pereira SL, Cohn RD, Wintle RF, Abuzenadah AM, Abu-Elmagd M, Scherer SW. Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome. BMC Genomics 2015;16 Suppl 1:S12. [PMID: 25923536 DOI: 10.1186/1471-2164-16-S1-S12] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
23 Lange S, Pinotsis N, Agarkova I, Ehler E. The M-band: The underestimated part of the sarcomere. Biochim Biophys Acta Mol Cell Res 2020;1867:118440. [PMID: 30738787 DOI: 10.1016/j.bbamcr.2019.02.003] [Cited by in Crossref: 28] [Cited by in F6Publishing: 24] [Article Influence: 9.3] [Reference Citation Analysis]
24 Yang LL, Liang SS. Study on pathogenic genes of dwarfism disease by next-generation sequencing. World J Clin Cases 2021; 9(7): 1600-1609 [PMID: 33728303 DOI: 10.12998/wjcc.v9.i7.1600] [Reference Citation Analysis]
25 Simsek-Kiper PO, Taskiran E, Kosukcu C, Arslan UE, Cormier-Daire V, Gonc N, Ozon A, Alikasifoglu A, Kandemir N, Utine GE, Alanay Y, Alikasifoglu M, Boduroglu K. Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome. Am J Med Genet A 2019;179:1157-72. [PMID: 30980518 DOI: 10.1002/ajmg.a.61154] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
26 Keskin M, Muratoğlu Şahin N, Kurnaz E, Bayramoğlu E, Savaş Erdeve Ş, Aycan Z, Çetinkaya S. A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene. J Clin Res Pediatr Endocrinol 2017;9:91-4. [PMID: 27796265 DOI: 10.4274/jcrpe.3238] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]