Genetic profiles are differentially expressed in muscle biopsies (MBx) from untreated children with juvenile dermatomyositis (JDM) with pathological calcifications (Ca++)

被引：0

作者：

Chen, YW

Pachman, LM

机构：

[1] George Washington Univ, Washington, DC 20052 USA

[2] Childrens Natl Med Ctr, Med Genet Res Ctr, Washington, DC 20010 USA

[3] Northwestern Univ, Childrens Mem Inst Educ & Res, Dept Pediat, Chicago, IL 60208 USA

来源：

PEDIATRIC RESEARCH | 2003年 / 53卷 / 04期

关键词：

D O I：

暂无

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：15A / 15A

页数：1

共 20 条

[1] Gene expression profiles in muscle biopsies (MBx) from untreated children with Juvenile Dermatomyositis (JDM) with pathological calcification (PCa++) compared to JDM without PCa++.
Pachman, LM
Chen, YW
[J]. ARTHRITIS AND RHEUMATISM, 2003, 48 (09): : S515 - S515
[2] Expression profiling in muscle from untreated children with juvenile dermatomyositis (JDM) with pathological calcifications.
Chen, YW
Pachman, LM
[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 528 - 528
[3] Expression of TNFα in muscle fibers in biopsies (MBx) from untreated juvenile dermatomyositis (JDM) is associated with the TNF-308A allele.
Fedczyna, TO
Lutz, JL
Caliendo, J
Pachman, LM
[J]. ARTHRITIS AND RHEUMATISM, 2000, 43 (09): : S276 - S276
[4] Duration of untreated juvenile dermatomyositis (JDM) at diagnosis: Impact on muscle biopsy (MBx) gene expression profiles, comparisons with polymyositis (PM)
Shrestha, Sheela
Shrestha, Sheela
Geraci, Nicholas
Morgan, Gabrielle
Chen, Yi-Wen
[J]. CLINICAL IMMUNOLOGY, 2008, 127 : S97 - S97
[5] Differential distribution of lymphocyte subpopulations in peripheral blood and muscle biopsies in untreated Juvenile Dermatomyositis (JDM)
Chuu, C
O'Gorman, M
Pachman, LM
[J]. CLINICAL IMMUNOLOGY, 2005, 115 : S258 - S258
[6] TRAIL mediated apoptosis in muscle biopsies from untreated children with juvenile dermatomyositis.
Fedczyna, TO
Lutz, JL
Pachman, LM
[J]. CLINICAL IMMUNOLOGY, 2002, 103 (03) : S47 - S47
[7] Increased CD8+ and CD56+ lymphocytes in untreated juvenile dermatomyositis (JDM) muscle biopsies (MBx) are associated with a short compared with a long disease duration.
Pachman, LM
Fedczyna, TO
Lutz, JL
Caliendo, J
Lechman, T
O'Gorman, MRG
[J]. ARTHRITIS AND RHEUMATISM, 2000, 43 (09): : S195 - S195
[8] Bone matrix proteins (osteopontin, bone sialoprotein, osteonectin, and bone acidic glycoprotein -5) in muscle biopsies from children with untreated juvenile dermatomyositis (JDM)
Pachman, LM
Krafft, KM
Fedezyna, TO
Lutz, JL
Gorska, JP
Shah, S
Barr, J
Webb, C
Raja, A
Veis, A
[J]. ARTHRITIS AND RHEUMATISM, 2001, 44 (09): : S264 - S264
[9] Studies of muscle biopsies (MBx) from DQA1*0501 untreated children with juvenile dermatomyositis (JDM) very early in their disease course:: evidence of a TCR Vβ8 motif and increased CD56+ NK cells
Pachman, LM
O'Gorman, MRG
Lawton, T
Liotta, M
Pope, RM
Greene, M
Wu, TT
[J]. ARTHRITIS AND RHEUMATISM, 1998, 41 (09): : S203 - S203
[10] Maternal microchimerism in muscle biopsies from children with Juvenile Dermatomyositis
Ramanan, A. V.
Gillespie, K. M.
Van Zyl, B.
Varsani, H.
Wedderburn, L. R.
[J]. CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2011, 29 (02) : 372 - 372

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