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標題: Titlebook: Genetics of Rare Autoimmune Diseases; Javier Martín,Francisco David Carmona Book 2019 Springer Nature Switzerland AG 2019 Genomics.Autoimm [打印本頁]

作者: 熱情美女    時間: 2025-3-21 17:13
書目名稱Genetics of Rare Autoimmune Diseases影響因子(影響力)




書目名稱Genetics of Rare Autoimmune Diseases影響因子(影響力)學科排名




書目名稱Genetics of Rare Autoimmune Diseases網絡公開度




書目名稱Genetics of Rare Autoimmune Diseases網絡公開度學科排名




書目名稱Genetics of Rare Autoimmune Diseases被引頻次




書目名稱Genetics of Rare Autoimmune Diseases被引頻次學科排名




書目名稱Genetics of Rare Autoimmune Diseases年度引用




書目名稱Genetics of Rare Autoimmune Diseases年度引用學科排名




書目名稱Genetics of Rare Autoimmune Diseases讀者反饋




書目名稱Genetics of Rare Autoimmune Diseases讀者反饋學科排名





作者: 植物學    時間: 2025-3-21 21:30

作者: Medley    時間: 2025-3-22 02:43

作者: 無意    時間: 2025-3-22 06:44
,Sj?gren’s Syndrome,ons. Indeed, even though keratoconjunctivitis sicca, resulting from the involvement of lacrimal glands, and xerostomia, resulting from the involvement of salivary glands, are usually prominent, pSS presents as a multifaceted and systemic condition with a broad variety of clinical manifestations. The
作者: 干涉    時間: 2025-3-22 10:34

作者: 原來    時間: 2025-3-22 14:45

作者: 原來    時間: 2025-3-22 19:20
Giant Cell Arteritis,ic factors may affect its susceptibility and phenotypic expression. During the last decades, a large number of candidate gene studies explored the genetic component of GCA. However, most genetic associations were inconsistent due to reduced sample sizes and lack of replication in independent populat
作者: Delirium    時間: 2025-3-22 21:38
Takayasu Arteritis,udes a preponderance of risk in East Asian, South Asian, and South American populations, as well as familial aggregation of the disease. The most reproduced genetic association with Takayasu arteritis is with the HLA-B*52 allele, with additional associations in the HLA region described across many e
作者: 有毒    時間: 2025-3-23 04:13
Primary Biliary Cirrhosis, Primary Sclerosing Cholangitis, and Autoimmune Hepatitis,langitis (PSC), and autoimmune hepatitis (AIH), are complex conditions in which both genetic and environmental factors may affect the hepatobiliary system. Until recently, risk HLA haplotypes were the only genetic factor identified in these diseases, which were insufficient to explain most of the di
作者: 妨礙議事    時間: 2025-3-23 09:36

作者: Foreknowledge    時間: 2025-3-23 13:03
Autoimmune Myasthenia Gravis,relatively well understood pathogenesis, the disease is heterogeneous. Disease subgroups are being diversified with respect to age at disease onset, clinical presentation, sex distribution, autoantigens, as well as associated thymic pathologies. Genetic susceptibility to MG was implicated by family
作者: 小畫像    時間: 2025-3-23 14:04
Common Genetic Component in Autoimmunity,ders and their etiology has not been fully elucidated yet, a number of these conditions share some common characteristics such as inflammation and the presence of autoantibodies and self-reactive T cells..Ten years ago, a better understanding of human genetic variation and advances in high-throughpu
作者: 索賠    時間: 2025-3-23 18:54

作者: 縫紉    時間: 2025-3-23 23:22
Systemic Lupus Erythematosus,rgeting. Both common and rare variants cannot, however, be viewed entirely independently, as modified penetrance of protein-coding variants through regulatory haplotypes, as well as common variant haplotypes, has been observed in SLE.
作者: dowagers-hump    時間: 2025-3-24 06:01
,Sj?gren’s Syndrome,munity. Most of the genes associated with susceptibility to pSS have been identified because the proteins involved have been previously associated with the pathogenesis of pSS or because the genes had already been associated with another autoimmune disease such as SLE or RA. Consequently, in this ch
作者: 磨碎    時間: 2025-3-24 06:44
Polymyositis/Dermatomyositis,unidentified, and, therefore, future efforts will be necessary to gain insight into this missing heritability, as well as on the functional consequences of associated variants. In addition, the role of epigenetic modifications in the IIM pathogenesis is being currently explored. Integrating genetics
作者: GLEAN    時間: 2025-3-24 12:37

作者: MAL    時間: 2025-3-24 18:30
Common Genetic Component in Autoimmunity, more robustly validated shared autoimmunity risk loci found in recent GWAS. More specifically, we discuss the involvement of the HLA and other shared risk loci such as the tumor necrosis factor cytokine and receptor superfamilies, IL23R and IL2RA, and genes involved in the interferon signature and
作者: Onerous    時間: 2025-3-24 19:57

作者: 碳水化合物    時間: 2025-3-25 02:44
Fruchts?fte, Limonaden, Brauselimonadenrgeting. Both common and rare variants cannot, however, be viewed entirely independently, as modified penetrance of protein-coding variants through regulatory haplotypes, as well as common variant haplotypes, has been observed in SLE.
作者: Anecdote    時間: 2025-3-25 04:00
Ergebnisse des Sieges von Gravelotte,munity. Most of the genes associated with susceptibility to pSS have been identified because the proteins involved have been previously associated with the pathogenesis of pSS or because the genes had already been associated with another autoimmune disease such as SLE or RA. Consequently, in this ch
作者: Immunotherapy    時間: 2025-3-25 08:57
,Getrennt marschieren — vereint schlagen,unidentified, and, therefore, future efforts will be necessary to gain insight into this missing heritability, as well as on the functional consequences of associated variants. In addition, the role of epigenetic modifications in the IIM pathogenesis is being currently explored. Integrating genetics
作者: 柱廊    時間: 2025-3-25 13:42
,Eheglück Aus Neurologischen Gründen,r from understanding the genetic implication in the disease. The determination of the “missing heritability,” the genetic factors that lead to the heterogeneity of the disease, the functional effects of the associated variants, and the definition of the pathways altered in MS are the actual focus of
作者: SPALL    時間: 2025-3-25 15:58

作者: Mercantile    時間: 2025-3-25 22:06
https://doi.org/10.1007/978-3-030-03934-9Genomics; Autoimmunity; Biomarkers; Systemic sclerosis; Systemic Lupus Erythematosus; Beh?et disease; Sjor
作者: Cloudburst    時間: 2025-3-26 01:34

作者: ELUDE    時間: 2025-3-26 05:58

作者: 強所    時間: 2025-3-26 10:12
https://doi.org/10.1007/978-3-540-49695-3r of vessels throughout the body which lead to significant organ involvement. This condition, given its low prevalence, is classified as a rare systemic vasculitis. Although its etiology remains unclear, it is known that it is a multifactorial and immune-mediated disease in which imbalances of the i
作者: Mercurial    時間: 2025-3-26 14:41

作者: 易發(fā)怒    時間: 2025-3-26 17:59

作者: 無彈性    時間: 2025-3-26 22:17
Im Garten, auf Wiese, Terrasse oder Balkon,iitis (MPA), granulomatosis with polyangiitis (GPA, formerly Wegener’s granulomatosis), and eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss syndrome). AAV can be considered a complex disease; in fact, both genetic and environmental factors are involved in its susceptibili
作者: 表主動    時間: 2025-3-27 02:36

作者: 泄露    時間: 2025-3-27 06:05

作者: 保守    時間: 2025-3-27 10:50
,Wesen des Nervenschu?schmerzes,langitis (PSC), and autoimmune hepatitis (AIH), are complex conditions in which both genetic and environmental factors may affect the hepatobiliary system. Until recently, risk HLA haplotypes were the only genetic factor identified in these diseases, which were insufficient to explain most of the di
作者: BUCK    時間: 2025-3-27 16:02

作者: ANNUL    時間: 2025-3-27 20:14
,Die L?sung des Besch?ftigungsproblems,relatively well understood pathogenesis, the disease is heterogeneous. Disease subgroups are being diversified with respect to age at disease onset, clinical presentation, sex distribution, autoantigens, as well as associated thymic pathologies. Genetic susceptibility to MG was implicated by family
作者: WAG    時間: 2025-3-27 23:25
H. C. Oppermann,L. Wille,H. E. Ulmerders and their etiology has not been fully elucidated yet, a number of these conditions share some common characteristics such as inflammation and the presence of autoantibodies and self-reactive T cells..Ten years ago, a better understanding of human genetic variation and advances in high-throughpu
作者: 尾隨    時間: 2025-3-28 03:03
Springer Nature Switzerland AG 2019
作者: drusen    時間: 2025-3-28 07:54
Genetics of Rare Autoimmune Diseases978-3-030-03934-9Series ISSN 2282-6505 Series E-ISSN 2283-6403
作者: 小淡水魚    時間: 2025-3-28 10:56

作者: 種族被根除    時間: 2025-3-28 17:43

作者: 間諜活動    時間: 2025-3-28 21:46
Studien zur Internationalen Politik immune-related genes, including ., ./., ., and .. Several of these variants have been shown to impact the regulation of their associated genes, playing a role in the incompletely understood etiology of Takayasu arteritis.
作者: LUDE    時間: 2025-3-29 02:35

作者: Intellectual    時間: 2025-3-29 05:57
2282-6505 t of autoimmunity.Written by renowned clinicians and researc.The main aim of this volume is to provide an updated overview of the genetic basis of a group of complex disorders that are considered rare individually, but show a relatively high prevalence on the whole in developed countries: the rare a
作者: 遣返回國    時間: 2025-3-29 09:41
Der Naturwissenschaftler als Unternehmerions. More recently, the establishment of international consortia and the use of the novel omic technologies have given a boost to the current knowledge of the pathological mechanisms behind GCA. In this chapter, we will give an updated overview of the recent insights into the genetic basis of GCA.
作者: 凹處    時間: 2025-3-29 14:29
,Wesen des Nervenschu?schmerzes,sease heritability. Nevertheless, thanks to the development of large-scale AILDs patient cohorts and the implementation of high-throughput methods such as genome-wide association studies (GWAS), a large number of genetic associations have emerged. In this chapter, we will provide an overview of the recent insights into genetic background of AILDs.
作者: Innocence    時間: 2025-3-29 16:20
Giant Cell Arteritis,ions. More recently, the establishment of international consortia and the use of the novel omic technologies have given a boost to the current knowledge of the pathological mechanisms behind GCA. In this chapter, we will give an updated overview of the recent insights into the genetic basis of GCA.
作者: lipoatrophy    時間: 2025-3-29 22:29

作者: 巧辦法    時間: 2025-3-30 00:31

作者: considerable    時間: 2025-3-30 07:23
https://doi.org/10.1007/978-3-540-49695-3ch harbors the strongest known susceptibility factors for this disease. Additionally, we will review the available data in non-HLA regions, highlighting the confirmed risk loci and summarizing those that are only suggested. Finally, we will provide an overview of the main molecular pathways involved in the development of this pathology.
作者: 漂泊    時間: 2025-3-30 08:28





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