141 related articles for article (PubMed ID: 37528877)
1. Severe congenital neutropenia due to jagunal homolog 1 (
Thomas S; Guenther G; Rowe JH; Platt CD; Shimamura A; Levy O; Ganapathi L
Front Pediatr; 2023; 11():1223191. PubMed ID: 37528877
[TBL] [Abstract][Full Text] [Related]
2. A rare case of syndromic severe congenital neutropenia: JAGN1 mutation.
Çipe FE; Aydoğmuş Ç; Baskın K; Keskindemirci G; Garncarz W; Boztuğ K
Turk J Pediatr; 2020; 62(2):326-331. PubMed ID: 32419428
[TBL] [Abstract][Full Text] [Related]
3. JAGN1 mutation with distinct clinical features; two case reports and literature review.
Hojabri M; Farsi Y; Jamee M; Abolhassani H; Khani HHK; Karimi A; Mesdaghi M; Chavoshzadeh Z; Sharafian S
BMC Pediatr; 2023 Apr; 23(1):206. PubMed ID: 37120535
[TBL] [Abstract][Full Text] [Related]
4. JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family.
Baris S; Karakoc-Aydiner E; Ozen A; Delil K; Kiykim A; Ogulur I; Baris I; Barlan IB
J Clin Immunol; 2015 May; 35(4):339-43. PubMed ID: 25851723
[TBL] [Abstract][Full Text] [Related]
5. Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child With Intermittent Neutropenia.
Cifaldi C; Serafinelli J; Petricone D; Brigida I; Di Cesare S; Di Matteo G; Chiriaco M; De Vito R; Palumbo G; Rossi P; Palma P; Cancrini C; Aiuti A; Finocchi A
J Pediatr Hematol Oncol; 2019 May; 41(4):e266-e269. PubMed ID: 30044346
[TBL] [Abstract][Full Text] [Related]
6. JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.
Boztug K; Järvinen PM; Salzer E; Racek T; Mönch S; Garncarz W; Gertz EM; Schäffer AA; Antonopoulos A; Haslam SM; Schieck L; Puchałka J; Diestelhorst J; Appaswamy G; Lescoeur B; Giambruno R; Bigenzahn JW; Elling U; Pfeifer D; Conde CD; Albert MH; Welte K; Brandes G; Sherkat R; van der Werff Ten Bosch J; Rezaei N; Etzioni A; Bellanné-Chantelot C; Superti-Furga G; Penninger JM; Bennett KL; von Blume J; Dell A; Donadieu J; Klein C
Nat Genet; 2014 Sep; 46(9):1021-7. PubMed ID: 25129144
[TBL] [Abstract][Full Text] [Related]
7. A crucial role for Jagunal homolog 1 in humoral immunity and antibody glycosylation in mice and humans.
Hagelkruys A; Wirnsberger G; Stadlmann J; Wöhner M; Horrer M; Vilagos B; Jonsson G; Kogler M; Tortola L; Novatchkova M; Bönelt P; Hoffmann D; Koglgruber R; Steffen U; Schett G; Busslinger M; Bergthaler A; Klein C; Penninger JM
J Exp Med; 2021 Jan; 218(1):. PubMed ID: 32930709
[TBL] [Abstract][Full Text] [Related]
8. JAGN1 is required for fungal killing in neutrophil extracellular traps: Implications for severe congenital neutropenia.
Khandagale A; Lazzaretto B; Carlsson G; Sundin M; Shafeeq S; Römling U; Fadeel B
J Leukoc Biol; 2018 Dec; 104(6):1199-1213. PubMed ID: 30106500
[TBL] [Abstract][Full Text] [Related]
9. Severe congenital neutropenia-associated JAGN1 mutations unleash a calpain-dependent cell death programme in myeloid cells.
Khandagale A; Holmlund T; Entesarian M; Nilsson D; Kalwak K; Klaudel-Dreszler M; Carlsson G; Henter JI; Nordenskjöld M; Fadeel B
Br J Haematol; 2021 Jan; 192(1):200-211. PubMed ID: 33206996
[TBL] [Abstract][Full Text] [Related]
10. Cyclic manner of neutropenia in a patient with
Cipe FE; Celiksoy MH; Erturk B; Aydogmus Ç
Pediatr Hematol Oncol; 2018 Apr; 35(3):181-185. PubMed ID: 30346863
[No Abstract] [Full Text] [Related]
11. JAGN1, tetraspanins, and Erv proteins: is common topology indicative of common function in cargo sorting?
VanWinkle PE; Parish F; Edwards YJK; Sztul E
Am J Physiol Cell Physiol; 2020 Oct; 319(4):C667-C674. PubMed ID: 32783652
[TBL] [Abstract][Full Text] [Related]
12. Jagunal homolog 1 is a critical regulator of neutrophil function in fungal host defense.
Wirnsberger G; Zwolanek F; Stadlmann J; Tortola L; Liu SW; Perlot T; Järvinen P; Dürnberger G; Kozieradzki I; Sarao R; De Martino A; Boztug K; Mechtler K; Kuchler K; Klein C; Elling U; Penninger JM
Nat Genet; 2014 Sep; 46(9):1028-33. PubMed ID: 25129145
[TBL] [Abstract][Full Text] [Related]
13. Manifestation of severe congenital neutropenia in the oral cavity. Case report.
Krasuska-Sławińska E; Klaudel-Dreszler M; Minota M; Pożyczka-Fedor M; Olczak-Kowalczyk D; Minko-Chojnowska I
Cent Eur J Immunol; 2013; 48(1):70-74. PubMed ID: 37206584
[TBL] [Abstract][Full Text] [Related]
14. Severe congenital neutropenia caused by the ELANE gene mutation in a Vietnamese boy with misdiagnosis of tuberculosis and autoimmune neutropenia: a case report.
Vu QV; Wada T; Tran TT; Ngo DN; Van Dinh T; Nguyen CH; Le HT; Yachie A; Nguyen SN
BMC Hematol; 2015; 15():2. PubMed ID: 25705433
[TBL] [Abstract][Full Text] [Related]
15. A JAGN1-associated severe congenital neutropenia zebrafish model revealed an altered G-CSFR signaling and UPR activation.
Doll L; Welte K; Skokowa J; Bajoghli B
Blood Adv; 2024 May; ():. PubMed ID: 38739706
[TBL] [Abstract][Full Text] [Related]
16. Novel
Jia Y; Yue C; Bradford K; Qing X; Panosyan EH; Gotesman M
J Pediatr Genet; 2020 Sep; 9(3):203-206. PubMed ID: 32714623
[TBL] [Abstract][Full Text] [Related]
17. Novel
Tran TT; Vu QV; Wada T; Yachie A; Le Thi Minh H; Nguyen SN
Case Rep Pediatr; 2018; 2018():2798621. PubMed ID: 30598852
[TBL] [Abstract][Full Text] [Related]
18. Severe congenital neutropenia or hyper-IgM syndrome? A novel mutation of CD40 ligand in a patient with severe neutropenia.
Rezaei N; Aghamohammadi A; Ramyar A; Pan-Hammarstrom Q; Hammarstrom L
Int Arch Allergy Immunol; 2008; 147(3):255-9. PubMed ID: 18594157
[TBL] [Abstract][Full Text] [Related]
19. Kostmann Syndrome With Neurological Abnormalities: A Case Report and Literature Review.
Lyu B; Lyu W; Zhang X
Front Pediatr; 2020; 8():586859. PubMed ID: 33381479
[No Abstract] [Full Text] [Related]
20. Novel G6PC3 Mutations in Patients with Congenital Neutropenia: Case Reports and Review of the Literature.
Maroufi SF; Shaka Z; Mojtabavi H; Sadeghalvad M; Rayzan E; Sedighi I; Shahkarami S; Najafi M; Rohlfs M; Klein C; Rezaei N
Endocr Metab Immune Disord Drug Targets; 2021; 21(9):1660-1668. PubMed ID: 34137364
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
