SERPINA1 Gene Polymorphism: Analysis of Patients Over 2 Years

被引：0
|
作者：
Rufino, M. C. [1 ]
Bartholo, T. [2 ]
Viana, A. [2 ]
Chaves, B. [2 ]
D'Elia, V. [2 ]
Costa, C. [2 ]
机构：
[1] Fac Med Petropolis, Rio De Janeiro, Brazil
[2] Univ Estado Rio De Janeiro, Rio De Janeiro, Brazil
来源：
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE | 2024年 / 209卷
关键词：
D O I：
暂无
中图分类号：
R4 [临床医学];
学科分类号：
1002 ; 100602 ;
摘要：
A3785
引用
收藏
页数：1
相关论文
共 50 条
  • [41] Whole exome sequencing in a juvenile idiopathic arthritis large family with SERPINA1 gene mutations
    Cyprian Popescu
    BMC Rheumatology, 6
  • [42] SERPINA1 Gene Promoter Is Differentially Methylated in Peripheral Blood Mononuclear Cells of Pregnant Women
    Rotondo, John Charles
    Oton-Gonzalez, Lucia
    Selvatici, Rita
    Rizzo, Paola
    Pavasini, Rita
    Campo, Gianluca Calogero
    Lanzillotti, Carmen
    Mazziotta, Chiara
    De Mattei, Monica
    Tognon, Mauro
    Martini, Fernanda
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2020, 8
  • [43] Increased Frequency of the M3 SERPINA1 Variant for AAT in Patients With COPD
    Kueppers, F.
    Bolla, S.
    Zhao, H.
    Mandapati, C.
    Chatila, W.
    Marchetti, N.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2023, 207
  • [44] Prevalence of common HFE and SERPINA1 mutations in patients with hepatocellular carcinoma in a Moroccan population
    Ezzikouri, Sayeh
    El Feydi, Abdellah Essaid
    El Kihal, Latifa
    Afifi, Rajae
    Benazzouz, Mustapha
    Hassar, Mohammed
    Chafik, Abdelaziz
    Pineau, Pascal
    Benjelloun, Soumaya
    ARCHIVES OF MEDICAL RESEARCH, 2008, 39 (02) : 236 - 241
  • [45] Heterozygous SERPINA1 defects and their impact on clinical manifestations of patients with predominantly antibody deficiencies
    Sarrou, Styliani
    Voulgaridi, Ioanna
    Fousika, Athanasia
    Dadouli, Katerina
    Margaritopoulou, Olympia
    Kakkas, Ioannis
    Hadjichristodoulou, Christos
    Kalala, Fani
    Speletas, Matthaios
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2024, 54 : 1036 - 1036
  • [46] Heterozygous SERPINA1 Defects and Their Impact on Clinical Manifestations of Patients with Predominantly Antibody Deficiencies
    Sarrou, Styliani
    Voulgaridi, Ioanna
    Fousika, Athanasia
    Dadouli, Katerina
    Margaritopoulou, Olympia
    Kakkas, Ioannis
    Hadjichristodoulou, Christos
    Kalala, Fani
    Speletas, Matthaios
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (10)
  • [47] Methylation of SERPINA1 gene promoter may predict chronic obstructive pulmonary disease in patients affected by acute coronary syndrome
    Rotondo, John Charles
    Aquila, Giorgio
    Oton-Gonzalez, Lucia
    Selvatici, Rita
    Rizzo, Paola
    De Mattei, Monica
    Pavasini, Rita
    Tognon, Mauro
    Campo, Gianluca Calogero
    Martini, Fernanda
    CLINICAL EPIGENETICS, 2021, 13 (01)
  • [48] Panniculitis as main clinical manifestation of alpha-1 antitrypsin deficiency revealing a SerpinA1 gene mutation
    Abdalla, Beatrice Martinez Zugaib
    Criado, Paulo Ricardo
    AUSTRALASIAN JOURNAL OF DERMATOLOGY, 2020, 61 (04) : E470 - E471
  • [49] Methylation of SERPINA1 gene promoter may predict chronic obstructive pulmonary disease in patients affected by acute coronary syndrome
    John Charles Rotondo
    Giorgio Aquila
    Lucia Oton-Gonzalez
    Rita Selvatici
    Paola Rizzo
    Monica De Mattei
    Rita Pavasini
    Mauro Tognon
    Gianluca Calogero Campo
    Fernanda Martini
    Clinical Epigenetics, 2021, 13
  • [50] Computational Tools to Assist in Analyzing Effects of the SERPINA1 Gene Variation on Alpha-1 Antitrypsin (AAT)
    Mroz, Jakub
    Pelc, Magdalena
    Mitusinska, Karolina
    Chorostowska-Wynimko, Joanna
    Jezela-Stanek, Aleksandra
    GENES, 2024, 15 (03)
12345