139 related articles for article (PubMed ID: 33867526)
1. Germline variants in UNC13D and AP3B1 are enriched in COVID-19 patients experiencing severe cytokine storms.
Luo H; Liu D; Liu W; Wang G; Chen L; Cao Y; Wei J; Xiao M; Liu X; Huang G; Wang W; Zhou J; Wang QF
Eur J Hum Genet; 2021 Aug; 29(8):1312-1315. PubMed ID: 33867526
[TBL] [Abstract][Full Text] [Related]
2. Synergistic defects of UNC13D and AP3B1 leading to adult hemophagocytic lymphohistiocytosis.
Gao L; Zhu L; Huang L; Zhou J
Int J Hematol; 2015 Oct; 102(4):488-92. PubMed ID: 25980904
[TBL] [Abstract][Full Text] [Related]
3. Sequence analysis of the SRGN, AP3B1, ARF6, and SH2D1A genes in familial hemophagocytic lymphohistiocytosis.
Ma D; Rudd E; Edner J; Gavhed S; Ramme KG; Fadeel B; Nordenskjöld M; Henter JI; Zheng C
Pediatr Blood Cancer; 2008 May; 50(5):1067-9. PubMed ID: 18000860
[TBL] [Abstract][Full Text] [Related]
4. Cytokine Storms in the Course of COVID-19 and Haemophagocytic Lymphohistiocytosis in Pregnant and Postpartum Women.
Obuchowska A; Standyło A; Obuchowska K; Kimber-Trojnar Ż; Leszczyńska-Gorzelak B
Biomolecules; 2021 Aug; 11(8):. PubMed ID: 34439868
[TBL] [Abstract][Full Text] [Related]
5. Genetic variant spectrum in 265 Chinese patients with hemophagocytic lymphohistiocytosis: Molecular analyses of PRF1, UNC13D, STX11, STXBP2, SH2D1A, and XIAP.
Chen X; Wang F; Zhang Y; Teng W; Wang M; Nie D; Zhou X; Wang D; Zhao H; Zhu P; Liu H
Clin Genet; 2018 Aug; 94(2):200-212. PubMed ID: 29665027
[TBL] [Abstract][Full Text] [Related]
6. Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis.
Mukda E; Trachoo O; Pasomsub E; Tiyasirichokchai R; Iemwimangsa N; Sosothikul D; Chantratita W; Pakakasama S
Int J Hematol; 2017 Aug; 106(2):282-290. PubMed ID: 28353193
[TBL] [Abstract][Full Text] [Related]
7. Hemophagocytic lymphohistiocytosis: a review inspired by the COVID-19 pandemic.
Soy M; Atagündüz P; Atagündüz I; Sucak GT
Rheumatol Int; 2021 Jan; 41(1):7-18. PubMed ID: 32588191
[TBL] [Abstract][Full Text] [Related]
8. Different functions of biogenesis of lysosomal organelles complex 3 subunit 1 (Hps1) and adaptor-related protein complex 3, beta 1 subunit (Ap3b1) genes on spermatogenesis and male fertility.
Jing R; Zhang H; Kong Y; Li K; Dong X; Yan J; Han J; Feng L
Reprod Fertil Dev; 2019 Apr; 31(5):972-982. PubMed ID: 30786955
[TBL] [Abstract][Full Text] [Related]
9. UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis.
Yoon HS; Kim HJ; Yoo KH; Sung KW; Koo HH; Kang HJ; Shin HY; Ahn HS; Kim JY; Lim YT; Bae KW; Lee KO; Shin JS; Lee ST; Chung HS; Kim SH; Park CJ; Chi HS; Im HJ; Seo JJ
Haematologica; 2010 Apr; 95(4):622-6. PubMed ID: 20015888
[TBL] [Abstract][Full Text] [Related]
10. Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II.
Enders A; Zieger B; Schwarz K; Yoshimi A; Speckmann C; Knoepfle EM; Kontny U; Müller C; Nurden A; Rohr J; Henschen M; Pannicke U; Niemeyer C; Nurden P; Ehl S
Blood; 2006 Jul; 108(1):81-7. PubMed ID: 16551969
[TBL] [Abstract][Full Text] [Related]
11. Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2.
Jones ML; Murden SL; Brooks C; Maloney V; Manning RA; Gilmour KC; Bharadwaj V; de la Fuente J; Chakravorty S; Mumford AD
BMC Med Genet; 2013 Apr; 14():42. PubMed ID: 23557002
[TBL] [Abstract][Full Text] [Related]
12. Could hemophagocytic lymphohistiocytosis be the core issue of severe COVID-19 cases?
Opoka-Winiarska V; Grywalska E; Roliński J
BMC Med; 2020 Jul; 18(1):214. PubMed ID: 32664932
[TBL] [Abstract][Full Text] [Related]
13. Genetic predisposition in patients with severe COVID-19.
Liu WB; Liu D; Yan J; Liu X; Wang QF
Yi Chuan; 2022 Aug; 44(8):672-681. PubMed ID: 36384666
[TBL] [Abstract][Full Text] [Related]
14. Partial albinism and immunodeficiency in patients with Hermansky-Pudlak Type II: Introducing 2 novel mutations.
Alizadeh Z; Nabilou S; Mazinani M; Tajik S; Hamidieh AA; Houshmand M; Fazlollahi MR; Pourpak Z
Scand J Immunol; 2021 Jan; 93(1):e12966. PubMed ID: 32869296
[No Abstract] [Full Text] [Related]
15. Novel AP3B1 mutations in a Hermansky-Pudlak syndrome type2 with neonatal interstitial lung disease.
Matsuyuki K; Ide M; Houjou K; Shima S; Tanaka S; Watanabe Y; Tomino H; Egashira T; Takayanagi T; Tashiro K; Okamura K; Suzuki T; Miyamoto T; Shibata H; Yasumi T; Nishikomori R
Pediatr Allergy Immunol; 2022 Feb; 33(2):e13748. PubMed ID: 35212049
[No Abstract] [Full Text] [Related]
16. Characterization of a novel splicing mutation in UNC13D gene through amplicon sequencing: a case report on HLH.
Liu D; Hu X; Jiang X; Gao B; Wan C; Chen C
BMC Med Genet; 2017 Nov; 18(1):135. PubMed ID: 29157204
[TBL] [Abstract][Full Text] [Related]
17. An overview of proteomic methods for the study of 'cytokine storms'.
David P; Hansen FJ; Bhat A; Weber GF
Expert Rev Proteomics; 2021 Feb; 18(2):83-91. PubMed ID: 33849358
[No Abstract] [Full Text] [Related]
18. Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding.
Fager Ferrari M; Leinoe E; Rossing M; Norström E; Strandberg K; Steen Sejersen T; Qvortrup K; Zetterberg E
Platelets; 2018 Jan; 29(1):56-64. PubMed ID: 28399723
[TBL] [Abstract][Full Text] [Related]
19. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
Zur Stadt U; Beutel K; Kolberg S; Schneppenheim R; Kabisch H; Janka G; Hennies HC
Hum Mutat; 2006 Jan; 27(1):62-8. PubMed ID: 16278825
[TBL] [Abstract][Full Text] [Related]
20. Novel AP3B1 compound heterozygous mutations in a Japanese patient with Hermansky-Pudlak syndrome type 2.
Nishikawa T; Okamura K; Moriyama M; Watanabe K; Ibusuki A; Sameshima S; Masamoto I; Yamazaki I; Tanita K; Kanekura T; Kanegane H; Suzuki T; Kawano Y
J Dermatol; 2020 Feb; 47(2):185-189. PubMed ID: 31820501
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]