Correction to: Diabetes, Renal, and Cardiovascular Disease in p47phox-/- Chronic Granulomatous Disease

被引：0
|
作者：
Hule, Gouri P. [1 ]
机构：
[1] Natl Inst Immunohaematol, Dept Pediat Immunol & Leukocyte Biol, Bombay 400012, Maharashtra, India
来源：
JOURNAL OF CLINICAL IMMUNOLOGY | 2018年 / 38卷 / 07期
关键词：
D O I：
10.1007/s10875-018-0547-2
中图分类号：
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号：
100102 ;
摘要：
引用
收藏
页码：737 / 738
页数：2
相关论文
共 50 条
  • [21] PERIPHERAL-BLOOD PROGENITORS AS A TARGET FOR GENETIC CORRECTION OF P47(PHOX)-DEFICIENT CHRONIC GRANULOMATOUS-DISEASE
    SEKHSARIA, S
    GALLIN, JI
    LINTON, GF
    MALLORY, RM
    MULLIGAN, RC
    MALECH, HL
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) : 7446 - 7450
  • [22] Two brothers with p47-phox-deficient chronic granulomatous disease associated with end-stage renal failure
    Yamazaki, H
    Nishi, S
    Chou, T
    Nakagawa, Y
    Shimada, H
    Nunoi, H
    ImajohOhmi, S
    Yoshioka, K
    Arakawa, M
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 1995, 10 (12) : 2334 - 2336
  • [23] RAPID DETECTION OF INTRACELLULAR P47PHOX AND P67PHOX BY FLOW CYTOMERY IN PATIENTS WITH CHRONIC GRANULOMATOUS DISEASE
    Wada, T.
    Muraoka, M.
    Toma, T.
    Shigemura, T.
    Agematsu, K.
    Moriuchi, H.
    Ohara, O.
    Morio, T.
    Yachie, A.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2012, 32 : 101 - 101
  • [24] Impaired p47phox phosphorylation in neutrophils from patients with p67phox-deficient chronic granulomatous disease
    Belambri, Sahra Amel
    Marzaioli, Viviana
    Hurtado-Nedelec, Margarita
    Pintard, Coralie
    Liang, Shiyu
    Liu, Yezhou
    Boussetta, Tarek
    Gougerot-Pocidalo, Marie-Anne
    Ye, Richard D.
    Dang, Pham My-Chan
    El-Benna, Jamel
    BLOOD, 2022, 139 (16) : 2512 - 2522
  • [25] The p47-phox gene has a pseudogene carrying the most common mutation for p47-phox deficient chronic granulomatous disease.
    Gorlach, A
    Roesler, J
    Hopkins, PJ
    Christensen, BL
    Lee, P
    Green, ED
    Chanock, SJ
    Curnutte, JT
    BLOOD, 1995, 86 (10) : 1027 - 1027
  • [26] Establishing the platform for clinical gene therapy of p47phox chronic granulomatous disease (CGD)
    Schejtman, A.
    Cutrim Arago Filho, W.
    Zinicola, M.
    Siler, U.
    Reichenbach, J.
    Gaspar, H. B.
    Condino-Neto, A.
    Thrasher, A. J.
    Santilli, G.
    HUMAN GENE THERAPY, 2016, 27 (11) : A114 - A115
  • [27] THE P47(PHOX) MOUSE KNOCK-OUT MODEL OF CHRONIC GRANULOMATOUS-DISEASE
    JACKSON, SH
    GALLIN, JI
    HOLLAND, SM
    JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (03): : 751 - 758
  • [28] Preclinical evaluation of the pCCLCHIM-p47 lentiviral vector for the gene therapy of p47phox deficient Chronic Granulomatous Disease
    Schejtman, A.
    Vetharoy, W.
    Choi, U.
    Rothe, M.
    Rivat, C.
    Piras, G.
    Benedetti, S.
    Santos, C. C.
    Schambach, A.
    Malech, H. L.
    Thrasher, A. J.
    Santilli, G.
    HUMAN GENE THERAPY, 2019, 30 (11) : A80 - A80
  • [29] Novel Diagnostic Tool for p47phox-Deficient Chronic Granulomatous Disease Patient and Carrier Detection
    Wrona, Dominik
    Siler, Ulrich
    Reichenbach, Janine
    MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT, 2019, 13 : 274 - 278
  • [30] Deficiency of p67(phox), p47(phox) or gp91(phox) in chronic granulomatous disease does not impair leucocyte chemotaxis or motility
    Zicha, D
    Dunn, GA
    Segal, AW
    BRITISH JOURNAL OF HAEMATOLOGY, 1997, 96 (03) : 543 - 550
12345