226 related articles for article (PubMed ID: 26769062)
21. TBL1XR1 Mutations Drive Extranodal Lymphoma by Inducing a Pro-tumorigenic Memory Fate.
Venturutti L; Teater M; Zhai A; Chadburn A; Babiker L; Kim D; Béguelin W; Lee TC; Kim Y; Chin CR; Yewdell WT; Raught B; Phillip JM; Jiang Y; Staudt LM; Green MR; Chaudhuri J; Elemento O; Farinha P; Weng AP; Nissen MD; Steidl C; Morin RD; Scott DW; Privé GG; Melnick AM
Cell; 2020 Jul; 182(2):297-316.e27. PubMed ID: 32619424
[TBL] [Abstract][Full Text] [Related]
22. Transducin (β)-like 1 X-linked receptor 1 promotes gastric cancer progression via the ERK1/2 pathway.
Zhou Q; Wang X; Yu Z; Wu X; Chen X; Li J; Zhu Z; Liu B; Su L
Oncogene; 2017 Mar; 36(13):1873-1886. PubMed ID: 27694893
[TBL] [Abstract][Full Text] [Related]
23. TBL1XR1 predicts isolated tumor cells and micrometastasis in patients with TNM stage I/II colorectal cancer.
Liu H; Liu Z; Li K; Li S; Song L; Gong Z; Shi W; Yang H; Xu Y; Ning S; Ismail S; Chen Y
J Gastroenterol Hepatol; 2017 Sep; 32(9):1570-1580. PubMed ID: 28127799
[TBL] [Abstract][Full Text] [Related]
24. Increased homozygosity in the first Hispanic patient with plantar lipomatosis, unusual facies, and developmental delay (Pierpont syndrome): a case report.
O'Keefe S; Wefuan DT; Humberson JB; Schmidt K; Wiley J
J Med Case Rep; 2016 Aug; 10(1):223. PubMed ID: 27520388
[TBL] [Abstract][Full Text] [Related]
25. Plantar lipomatosis, unusual facies, and developmental delay: confirmation of Pierpont syndrome.
Oudesluijs GG; Hordijk R; Boon M; Sijens PE; Hennekam RC
Am J Med Genet A; 2005 Aug; 137(1):77-80. PubMed ID: 16007632
[TBL] [Abstract][Full Text] [Related]
26. Correlations between TBL1XR1 and recurrence of colorectal cancer.
Liu H; Xu Y; Zhang Q; Li K; Wang D; Li S; Ning S; Yang H; Shi W; Liu Z; Chen Y
Sci Rep; 2017 Mar; 7():44275. PubMed ID: 28295012
[TBL] [Abstract][Full Text] [Related]
27. Expanding the genotypic and phenotypic spectrum associated with TBL1XR1 de novo variants.
Ren M; Zheng H; Lu X; Lian W; Feng B
Gene; 2023 Nov; 886():147777. PubMed ID: 37683765
[TBL] [Abstract][Full Text] [Related]
28. A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation.
Saitsu H; Tohyama J; Walsh T; Kato M; Kobayashi Y; Lee M; Tsurusaki Y; Miyake N; Goto Y; Nishino I; Ohtake A; King MC; Matsumoto N
J Hum Genet; 2014 Oct; 59(10):581-3. PubMed ID: 25102098
[TBL] [Abstract][Full Text] [Related]
29. Rare variant of TBL1XR1 in West syndrome: A case report.
Shen Y; Yuan M; Luo H; Yang Z; Liang M; Gan J
Mol Genet Genomic Med; 2022 Jul; 10(7):e1991. PubMed ID: 35611576
[TBL] [Abstract][Full Text] [Related]
30. Novel Arthrogryposis Multiplex Congenita Presentation in a Newborn With Pierpont Syndrome.
Pereira-Nunes J; Vilan A; Grangeia A; d'Oliveira R
J Investig Med High Impact Case Rep; 2023; 11():23247096221150637. PubMed ID: 36691917
[TBL] [Abstract][Full Text] [Related]
31. Expanding the spectrum of TBL1XR1 deletion: Report of a patient with brain and cardiac malformations.
Vaqueiro AC; de Oliveira CP; Cordoba MS; Versiani BR; de Carvalho CX; Alves Rodrigues PG; de Oliveira SF; Mazzeu JF; Pic-Taylor A
Eur J Med Genet; 2018 Jan; 61(1):29-33. PubMed ID: 29038029
[TBL] [Abstract][Full Text] [Related]
32. Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing.
Andersson E; Eldfors S; Edgren H; Ellonen P; Väkevä L; Ranki A; Mustjoki S
Exp Dermatol; 2014 May; 23(5):366-8. PubMed ID: 24689486
[TBL] [Abstract][Full Text] [Related]
33. Recurrent mutations of MYD88 and TBL1XR1 in primary central nervous system lymphomas.
Gonzalez-Aguilar A; Idbaih A; Boisselier B; Habbita N; Rossetto M; Laurenge A; Bruno A; Jouvet A; Polivka M; Adam C; Figarella-Branger D; Miquel C; Vital A; Ghesquières H; Gressin R; Delwail V; Taillandier L; Chinot O; Soubeyran P; Gyan E; Choquet S; Houillier C; Soussain C; Tanguy ML; Marie Y; Mokhtari K; Hoang-Xuan K
Clin Cancer Res; 2012 Oct; 18(19):5203-11. PubMed ID: 22837180
[TBL] [Abstract][Full Text] [Related]
34. The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1.
Parker H; An Q; Barber K; Case M; Davies T; Konn Z; Stewart A; Wright S; Griffiths M; Ross FM; Moorman AV; Hall AG; Irving JA; Harrison CJ; Strefford JC
Genes Chromosomes Cancer; 2008 Dec; 47(12):1118-25. PubMed ID: 18767146
[TBL] [Abstract][Full Text] [Related]
35. Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders.
Quan Y; Zhang Q; Chen M; Wu H; Ou J; Shen Y; Li K; Xun G; Zhao J; Hu Z; Xia K; Guo H
J Mol Neurosci; 2020 Dec; 70(12):2085-2092. PubMed ID: 32524419
[TBL] [Abstract][Full Text] [Related]
36. Deficiency of TBL1XR1 causes asthenozoospermia.
Zhou Q; Xu M; Wang X; Yu M; Chen X; Lu J; Zhou R; Zhang J; Ling X; Ji J
Andrologia; 2021 Apr; 53(3):e13980. PubMed ID: 33528066
[TBL] [Abstract][Full Text] [Related]
37. Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes.
Zaghlula M; Glaze DG; Enns GM; Potocki L; Schwabe AL; Suter B
Am J Med Genet A; 2018 Jul; 176(7):1683-1687. PubMed ID: 29777588
[No Abstract] [Full Text] [Related]
38. Fusion of the TBL1XR1 and HMGA1 genes in splenic hemangioma with t(3;6)(q26;p21).
Panagopoulos I; Gorunova L; Bjerkehagen B; Lobmaier I; Heim S
Int J Oncol; 2016 Mar; 48(3):1242-50. PubMed ID: 26708416
[TBL] [Abstract][Full Text] [Related]
39. Prognostic significance of TBL1XR1 in predicting liver metastasis for early stage colorectal cancer.
Liu H; Xu Y; Zhang Q; Yang H; Shi W; Liu Z; Li K; Gong Z; Ning S; Li S; Chen Y
Surg Oncol; 2017 Mar; 26(1):13-20. PubMed ID: 28317580
[TBL] [Abstract][Full Text] [Related]
40. Loss of TBL1XR1 disrupts glucocorticoid receptor recruitment to chromatin and results in glucocorticoid resistance in a B-lymphoblastic leukemia model.
Jones CL; Bhatla T; Blum R; Wang J; Paugh SW; Wen X; Bourgeois W; Bitterman DS; Raetz EA; Morrison DJ; Teachey DT; Evans WE; Garabedian MJ; Carroll WL
J Biol Chem; 2014 Jul; 289(30):20502-15. PubMed ID: 24895125
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
