Results 121 to 130 of about 806 (131)

Identification of thyroxine-binding globulin as a candidate plasma marker of chronic obstructive pulmonary disease [PDF]

core   +2 more sources

Receptor-independent regulation of Gα13 by alpha-1-antitrypsin C-terminal peptides. [PDF]

J Biol Chem
Park Y, Matsumoto S, Ogata K, Ma B, Kanada R, Isaka Y, Arichi N, Liang X, Maki R, Kozasa T, Okuno Y, Ohno H, Ishihama Y, Toyoshima F.   +13 more
europepmc   +1 more source

Alpha-1 Antitrypsin Genotype Distribution in Patients with Emphysema. [PDF]

Int J Chron Obstruct Pulmon Dis
Özdemir L, Gegin S, Özdemir B, Aksu EA, Pazarlı AC.   +4 more
europepmc   +1 more source

Phenotypic Expression of Respiratory Diseases and Tailored Treatment in Patients with Intermediate Alpha-1 Antitrypsin Deficiency: Evidence from a Retrospective Analysis of a Selected Cohort of Patients. [PDF]

Medicina (Kaunas)
Annunziata A, Fiorentino G, Simioli F, Atripaldi L, Balestrino M, Zuccarini G, Piras B, Libra A, Pino F, Di Micco P, Siniscalchi C, Ferrarotti I, Aronne L, Manzo R, Vancheri C, Calabrese C.   +15 more
europepmc   +1 more source

Genexpressionsanalyse von HOX-Genen und Genen der Tumor Stroma-Interaktion in humanen, serösen Ovarialkarzinomen [PDF]

, 2008
Pfeifer, Christian
core  

Persistent immune, coagulation and cardiac dysregulation are correlated with later post-discharge mortality in children with severe malnutrition. [PDF]

BMC Med
Kamau B, Mudibo EO, Wechessa C, Omer E, Gichuki BM, Mburu DM, Mwalekwa L, Timbwa M, Thitiri J, Ngari MM, Berkley JA, Njunge JM.   +11 more
europepmc   +1 more source

Skewed adaptive immune responses are involved in alpha-1 antitrypsin deficiency emphysema. [PDF]

Eur Respir J
Rojas-Quintero J, Ochsner SA, Lee HS, Cong C, Waich Cohen A, Colborg AS, Tsoyi K, Basil MC, Cantu E, Rosas IO, McKenna NJ, San-José Estépar R, Barjaktarevic I, Wilson AA, Polverino F.   +14 more
europepmc   +1 more source

Maternal and Fetal SERPINA3 Polymorphisms and Risk of Preeclampsia: A Dyad and Triad Based Case-Control Study. [PDF]

Curr Issues Mol Biol
Yang HH, Baldauf C, Pickering TA, Gjessing HK, Ingles SA, Wilson ML.   +5 more
europepmc   +1 more source

Plasma Exosomal-Derived SERPINA1 and GNAI2 Downregulation as Potential Diagnostic Biomarkers of Kawasaki Disease with Coronary Artery Aneurysms. [PDF]

Int J Mol Sci
Zheng Y, Bai B, Wei Z, Zhang M, Zhang Q, Li X.   +5 more
europepmc   +1 more source

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A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis

Lung, 2017
Alpha-1-antitrypsin deficiency (AATD) is a genetic condition caused by SERPINA1 mutations, which culminates into lower protease inhibitor activity in the serum and predisposes to emphysema. Clinical manifestations of AATD are often associated to ZZ (p.Glu342Lys) and SZ (p.Glu264Val) genotypes and less frequently to rare deficiency or null alleles in ...
G. E. Carpagnano, R. Santacroce, G. A. Palmiotti, A. Leccese, E. Giuffreda, M. Margaglione, M. P. Foschino Barbaro, S. Aliberti, D. Lacedonia   +8 more
openaire   +5 more sources