These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 33446651)

  • 1. Novel TNFAIP3 microdeletion in a girl with infantile-onset inflammatory bowel disease complicated by a severe perianal lesion.
    Taniguchi K; Inoue M; Arai K; Uchida K; Migita O; Akemoto Y; Hirayama J; Takeuchi I; Shimizu H; Hata K
    Hum Genome Var; 2021 Jan; 8(1):1. PubMed ID: 33446651
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
    Tsuchida N; Kirino Y; Soejima Y; Onodera M; Arai K; Tamura E; Ishikawa T; Kawai T; Uchiyama T; Nomura S; Kobayashi D; Taguri M; Mitsuhashi S; Mizuguchi T; Takata A; Miyake N; Nakajima H; Miyatake S; Matsumoto N
    Arthritis Res Ther; 2019 Jun; 21(1):137. PubMed ID: 31164164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expanding the spectrum of A20 haploinsufficiency in two Chinese families: cases report.
    Li GM; Liu HM; Guan WZ; Xu H; Wu BB; Sun L
    BMC Med Genet; 2019 Jul; 20(1):124. PubMed ID: 31299923
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Infantile Onset Intractable Inflammatory Bowel Disease Due to Novel Heterozygous Mutations in TNFAIP3 (A20).
    Zheng C; Huang Y; Ye Z; Wang Y; Tang Z; Lu J; Wu J; Zhou Y; Wang L; Huang Z; Yang H; Xue A
    Inflamm Bowel Dis; 2018 Nov; 24(12):2613-2620. PubMed ID: 29788367
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case Report: A novel mutation in
    Cao C; Fu X; Wang X
    Front Endocrinol (Lausanne); 2023; 14():1131437. PubMed ID: 37324276
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A20 Haploinsufficiency in a Chinese Patient With Intestinal Behcet's Disease-Like Symptoms: A Case Report.
    Chen Y; Huang H; He Y; Chen M; Seidler U; Tian D; Xiao F
    Front Immunol; 2020; 11():1414. PubMed ID: 32719680
    [No Abstract]   [Full Text] [Related]  

  • 7. Association of Clinical Phenotypes in Haploinsufficiency A20 (HA20) With Disrupted Domains of A20.
    Chen Y; Ye Z; Chen L; Qin T; Seidler U; Tian D; Xiao F
    Front Immunol; 2020; 11():574992. PubMed ID: 33101300
    [No Abstract]   [Full Text] [Related]  

  • 8. TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases.
    Aslani N; Asnaashari K; Parvaneh N; Shahrooei M; Sotoudeh-Anvari M; Shahram F; Ziaee V
    Pediatr Rheumatol Online J; 2022 Sep; 20(1):78. PubMed ID: 36064566
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of the TNFAIP3 in A20 haploinsufficiency: A case report.
    Yan M; Li D; Aknai S; Zhu H; Abudureyim M
    Medicine (Baltimore); 2021 May; 100(20):e25954. PubMed ID: 34011076
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A20 haploinsufficiency in a neonate caused by a large deletion on chromosome 6q.
    Zhang F; Zhang L
    Pediatr Rheumatol Online J; 2024 Jan; 22(1):12. PubMed ID: 38183052
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Haploinsufficiency of A20 (HA20): updates on the genetics, phenotype, pathogenesis and treatment.
    Yu MP; Xu XS; Zhou Q; Deuitch N; Lu MP
    World J Pediatr; 2020 Dec; 16(6):575-584. PubMed ID: 31587140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Three Chinese pedigrees of A20 haploinsufficiency: clinical, cytokine and molecular characterization.
    Tian Y; Wu B; Peng L; Wang J; Shen M
    Front Immunol; 2022; 13():955079. PubMed ID: 35958611
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel missense mutation in TNFAIP3 causes haploinsufficiency of A20.
    Jiang W; Deng M; Gan C; Wang L; Mao H; Li Q
    Cell Immunol; 2022 Jan; 371():104453. PubMed ID: 34808442
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The First Case of an Infant with Familial A20 Haploinsufficiency in Korea.
    Kim HY; Song JY; Kim WI; Ko HC; Park SE; Jang JH; Kim SH
    J Korean Med Sci; 2020 Aug; 35(30):e252. PubMed ID: 32743991
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel loss-of-function mutations in
    Zhang C; Han X; Sun L; Yang S; Peng J; Chen Y; Jin Y; Xu F; Liu Z; Zhou Q
    Clin Kidney J; 2022 Nov; 15(11):2027-2038. PubMed ID: 36325013
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A20 Haploinsufficiency in East Asia.
    Kadowaki T; Kadowaki S; Ohnishi H
    Front Immunol; 2021; 12():780689. PubMed ID: 34899744
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A report of clinical characteristics of 2 Chinese pedigrees with haploinsufficiency of A20 and literature review].
    Zhong LQ; Wang W; Wang L; Jiang JJ; Shen M; Song HM
    Zhonghua Er Ke Za Zhi; 2019 Dec; 57(12):922-927. PubMed ID: 31795558
    [No Abstract]   [Full Text] [Related]  

  • 18. Haploinsufficiency of A20 in a Chinese child caused by loss-of-function mutations in TNFAIP3: A case report and review of the literature.
    Liu J; Lin Y; Li X; Ba H; He X; Peng H; Li S; Zhu L
    Front Pediatr; 2022; 10():990008. PubMed ID: 36727002
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haploinsufficiency of A20 caused by a novel pathogenic missense variant of TNFAIP3 and successfully treated with anti-TNF and immunosuppressive therapies.
    Lina S; Ya'nan H; Ying Y; Fengfan W; Xin H; Xiaoxia R; Ying F
    Cell Immunol; 2023; 391-392():104753. PubMed ID: 37535999
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Functional analysis of novel A20 variants in patients with atypical inflammatory diseases.
    Kadowaki S; Hashimoto K; Nishimura T; Kashimada K; Kadowaki T; Kawamoto N; Imai K; Okada S; Kanegane H; Ohnishi H
    Arthritis Res Ther; 2021 Feb; 23(1):52. PubMed ID: 33549127
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.