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PCR Analysis to Identify AAT Gene Promoters and Splice Variants

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2750, p.33

Kalsheker, Noor

2024

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A DNA Algorithm for Calculating the Maximum Flow of a Network

Foundations of computing and decision sciences, 2023-12, Vol.48 (4), p.483-506

2023

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Alpha-1-Antitrypsin Deficiency: Biology, Diagnosis, Clinical Significance, and Emerging Therapies

1, 2017

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The Role of Alpha1-Antitrypsin Deficiency in Respiratory Disease

Anti-inflammatory & anti-allergy agents in medicinal chemistry, 2010-12, Vol.9 (4), p.299-303

Kalsheker, Noor

2010

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Identification of SPARC-like 1 protein as part of a biomarker panel for Alzheimer's disease in cerebrospinal fluid

Journal of Alzheimer's disease, 2012-01, Vol.28 (3), p.625-636

2012

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Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS)

Neurobiology of aging, 2012-08, Vol.33 (8), p.1849.e5-1849.e18

2012

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The role of IREB2 and transforming growth factor beta-1 genetic variants in COPD: a replication case-control study

BMC medical genetics, 2011-02, Vol.12 (1), p.24-24, Article 24

2011

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Copy number variation of the beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma

PloS one, 2014-01, Vol.9 (1), p.e84192-e84192

2014

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Association of MMP - 12 polymorphisms with severe and very severe COPD: A case control study of MMPs - 1, 9 and 12 in a European population

BMC medical genetics, 2010-01, Vol.11 (1), p.7-7

2010

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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

Nature communications, 2020-11, Vol.11 (1), p.5976-14, Article 5976

2020

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Variants in the fetal genome near FLT1 are associated with risk of preeclampsia

Nature genetics, 2017-08, Vol.49 (8), p.1255-1260

2017

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Opportunities and Challenges in the Genetics of COPD 2010: An International COPD Genetics Conference Report

Chronic obstructive pulmonary disease, 2011-04, Vol.8 (2), p.121-135

2011

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Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

Nature genetics, 2019-03, Vol.51 (3), p.494-505

2019

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A new promoter polymorphism in the alpha-1-antichymotrypsin gene is a disease modifier of Alzheimer’s disease

Neurobiology of aging, 2005-04, Vol.26 (4), p.449-453

2005

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SERPINA3 (aka alpha-1-antichymotrypsin)

Frontiers in bioscience, 2007-05, Vol.12 (8-12), p.2821

2007

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A study of three candidate genes for pre-eclampsia in a Sinhalese population from Sri Lanka

The journal of obstetrics and gynaecology research, 2009-04, Vol.35 (2), p.234-242

2009

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Guidance for laboratories performing molecular pathology for cancer patients

Journal of clinical pathology, 2014-11, Vol.67 (11), p.923-931

2014

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Amyloid precursor protein (APP) and the biology of proteolytic processing: relevance to Alzheimer’s disease

International Journal of Biochemistry and Cell Biology, 2003-11, Vol.35 (11), p.1505-1535

2003

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A novel monoclonal antibody to characterize pathogenic polymers in liver disease associated with α1‐antitrypsin deficiency

Hepatology (Baltimore, Md.), 2010-09, Vol.52 (3), p.1078-1088

2010

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Serpins: structure, function and molecular evolution

International Journal of Biochemistry and Cell Biology, 2003-11, Vol.35 (11), p.1536-1547

2003

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Oncostatin M induced α1-antitrypsin (AAT) gene expression in Hep G2 cells is mediated by a 3′ enhancer

Biochemical journal, 2002-07, Vol.365 (2), p.555-560

2002

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Mutation in an α1-antitrypsin enhancer results in an interleukin-6 deficient acute-phase response due to loss of cooperativity between transcription factors

Biochimica et biophysica acta. Molecular basis of disease, 1997-11, Vol.1362 (1), p.67-76

1997

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Matrix metalloproteinase-12 (MMP-12) SNP affects MMP activity, lung macrophage infiltration and protects against emphysema in COPD

Thorax, 2011-11, Vol.66 (11), p.970-976

2011

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Angiotensin-converting enzyme insertion-deletion polymorphism in normotensive and pre-eclamptic pregnancies

Journal of hypertension, 1999-06, Vol.17 (6), p.765-768

1999

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A polymorphism of the alpha1‐antitrypsin gene represents a risk factor for liver disease

Hepatology (Baltimore, Md.), 2008-01, Vol.47 (1), p.127-132

2008

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PCR Analysis to Identify AAT Gene Promoters and Splice Variants

A DNA Algorithm for Calculating the Maximum Flow of a Network

Alpha-1-Antitrypsin Deficiency: Biology, Diagnosis, Clinical Significance, and Emerging Therapies

The Role of Alpha1-Antitrypsin Deficiency in Respiratory Disease

Identification of SPARC-like 1 protein as part of a biomarker panel for Alzheimer's disease in cerebrospinal fluid

Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS)

The role of IREB2 and transforming growth factor beta-1 genetic variants in COPD: a replication case-control study

Copy number variation of the beta-defensin genes in europeans: no supporting evidence for association with lung function, chronic obstructive pulmonary disease or asthma

Association of MMP - 12 polymorphisms with severe and very severe COPD: A case control study of MMPs - 1, 9 and 12 in a European population

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

Variants in the fetal genome near FLT1 are associated with risk of preeclampsia

Opportunities and Challenges in the Genetics of COPD 2010: An International COPD Genetics Conference Report

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

A new promoter polymorphism in the alpha-1-antichymotrypsin gene is a disease modifier of Alzheimer’s disease

SERPINA3 (aka alpha-1-antichymotrypsin)

A study of three candidate genes for pre-eclampsia in a Sinhalese population from Sri Lanka

Guidance for laboratories performing molecular pathology for cancer patients

Amyloid precursor protein (APP) and the biology of proteolytic processing: relevance to Alzheimer’s disease

A novel monoclonal antibody to characterize pathogenic polymers in liver disease associated with α1‐antitrypsin deficiency

Serpins: structure, function and molecular evolution

Oncostatin M induced α1-antitrypsin (AAT) gene expression in Hep G2 cells is mediated by a 3′ enhancer

Mutation in an α1-antitrypsin enhancer results in an interleukin-6 deficient acute-phase response due to loss of cooperativity between transcription factors

Matrix metalloproteinase-12 (MMP-12) SNP affects MMP activity, lung macrophage infiltration and protects against emphysema in COPD

Angiotensin-converting enzyme insertion-deletion polymorphism in normotensive and pre-eclamptic pregnancies

A polymorphism of the alpha1‐antitrypsin gene represents a risk factor for liver disease

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