BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 26243289)

  • 1. Quantitation of circulating wild-type alpha-1-antitrypsin in heterozygous carriers of the S and Z deficiency alleles.
    Donato LJ; Karras RM; Katzmann JA; Murray DL; Snyder MR
    Respir Res; 2015 Aug; 16(1):96. PubMed ID: 26243289
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Alpha-1-Antitrypsin (A1AT) Proteotyping by LC-MS/MS.
    Kemp J; Ladwig PM; Snyder MR
    Methods Mol Biol; 2024; 2750():95-106. PubMed ID: 38108970
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Simultaneous phenotyping and quantification of α-1-antitrypsin by liquid chromatography-tandem mass spectrometry.
    Chen Y; Snyder MR; Zhu Y; Tostrud LJ; Benson LM; Katzmann JA; Bergen HR
    Clin Chem; 2011 Aug; 57(8):1161-8. PubMed ID: 21636698
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Reference and interpretive ranges for α(1)-antitrypsin quantitation by phenotype in adult and pediatric populations.
    Donato LJ; Jenkins SM; Smith C; Katzmann JA; Snyder MR
    Am J Clin Pathol; 2012 Sep; 138(3):398-405. PubMed ID: 22912357
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Null
    Chen S; DeMarco ML; Estey MP; Kyle B; Parker ML; Agbor TA; Kawada P; Speevak M; Nelson TN; Mattman A
    Clin Biochem; 2020 May; 79():23-27. PubMed ID: 32087139
    [TBL] [Abstract][Full Text] [Related]  

  • 6. α-1 Antitrypsin Genotype-Phenotype Discrepancy in a 42-Year-Old Man Who Carries the Null-Allele.
    Pavičić T; Ćelap I; Njegovan M; Tešija Kuna A; Štefanović M
    Lab Med; 2020 May; 51(3):301-305. PubMed ID: 31583408
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical heterogeneity and potential high pathogenicity of the Mmalton Alpha 1 antitrypsin allele at the homozygous, compound heterozygous and heterozygous states.
    Joly P; Guillaud O; Hervieu V; Francina A; Mornex JF; Chapuis-Cellier C
    Orphanet J Rare Dis; 2015 Oct; 10():130. PubMed ID: 26446624
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Place of genotyping in addition to the phenotype and the assay of serum α-1 antitrypsin].
    Joly P; Francina A; Lacan P; Heraut J; Chapuis-Cellier C
    Ann Biol Clin (Paris); 2011; 69(5):571-6. PubMed ID: 22008137
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Increased prevalence of the alpha-1-antitrypsin (A1AT) deficiency-related S gene in patients infected with human immunodeficiency virus type 1.
    Ferreira TC; Sampaio EP; Argañaraz GA; Gondim MV; Shapiro L; Argañaraz ER
    J Med Virol; 2014 Jan; 86(1):23-9. PubMed ID: 24122823
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Polymerase chain reaction detection of S and Z alpha-1-antitrypsin variants by duplex PCR assay.
    Lucotte G; Sesboüé R
    Mol Cell Probes; 1999 Oct; 13(5):389-91. PubMed ID: 10508561
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intrahepatic heteropolymerization of M and Z alpha-1-antitrypsin.
    Laffranchi M; Elliston EL; Miranda E; Perez J; Ronzoni R; Jagger AM; Heyer-Chauhan N; Brantly ML; Fra A; Lomas DA; Irving JA
    JCI Insight; 2020 Jul; 5(14):. PubMed ID: 32699193
    [TBL] [Abstract][Full Text] [Related]  

  • 12. How Can We Improve the Detection of Alpha1-Antitrypsin Deficiency?
    Ferrarotti I; Poplawska-Wisniewska B; Trevisan MT; Koepke J; Dresel M; Koczulla R; Ottaviani S; Baldo R; Gorrini M; Sala G; Cavallon L; Welte T; Chorostowska-Wynimko J; Luisetti M; Janciauskiene S
    PLoS One; 2015; 10(8):e0135316. PubMed ID: 26270547
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alpha-1 antitrypsin deficiency: From the lung to the heart?
    Curjuric I; Imboden M; Bettschart R; Caviezel S; Dratva J; Pons M; Rothe T; Schmidt-Trucksäss A; Stolz D; Thun GA; von Eckardstein A; Kronenberg F; Ferrarotti I; Probst-Hensch NM
    Atherosclerosis; 2018 Mar; 270():166-172. PubMed ID: 29432934
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Normal Alpha-1-Antitrypsin Variants Display in Serum Allele-Specific Protein Levels.
    Jager S; Cramer DAT; Heck AJR
    J Proteome Res; 2023 Apr; 22(4):1331-1338. PubMed ID: 36946534
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Polymerase chain reaction-mediated site-directed mutagenesis detection of Z and S alpha-1-antitrypsin alleles in family members.
    Hammerberg G; Keren DF
    J Clin Lab Anal; 1996; 10(6):384-8. PubMed ID: 8951606
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Outcomes of Living-donor Liver Transplantation Using Grafts Heterozygous for α-1 Antitrypsin Gene Mutations.
    Doshi SD; Wood L; Abt PL; Olthoff KM; Shaked A; Goldberg DS; Bittermann T
    Transplantation; 2019 Jun; 103(6):1175-1180. PubMed ID: 30335698
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The incidence of alpha-1-antitrypsin (A1AT) deficiency alleles in population of Central Poland--preliminary results from newborn screening].
    Chorostowska-Wynimko J; Struniawski R; Popławska B; Borszewska-Kornacka M
    Pneumonol Alergol Pol; 2012; 80(5):450-3. PubMed ID: 22926906
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage analysis of alpha 1-antitrypsin deficiency: lessons for complex diseases.
    Silverman EK; Mosley JD; Rao DC; Palmer LJ; Province MA; Elston RC; Weiss ST; Campbell EJ
    Hum Hered; 2001; 52(4):223-32. PubMed ID: 11713419
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of Rare Alpha-1 Antitrypsin Variants in Polish Patients with Chronic Respiratory Disorders.
    Duk K; Zdral A; Szumna B; Roży A; Chorostowska-Wynimko J
    Adv Exp Med Biol; 2016; 910():47-53. PubMed ID: 26987331
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid screening for alpha1-antitrypsin deficiency in patients with chronic obstructive pulmonary disease using dried blood specimens.
    Rodriguez F; Jardí R; Costa X; Cotrina M; Galimany R; Vidal R; Miravitlles M
    Am J Respir Crit Care Med; 2002 Sep; 166(6):814-7. PubMed ID: 12231490
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.