140 related articles for article (PubMed ID: 16435226)
1. Genetic variants of transferrin in the diagnosis of protein hypoglycosylation.
Albahri Z; Marklová E; Vanícek H; Minxová L; Dédek P; Skálová S
J Inherit Metab Dis; 2005; 28(6):1184-8. PubMed ID: 16435226
[TBL] [Abstract][Full Text] [Related]
2. Genetic variants of transferrin in cystic fibrosis.
Marklová E; Albahri Z; Vanícek H; Dedek P; Valis M; Kopácová M; Vávrová V
J Inherit Metab Dis; 2008 Jun; 31(3):457-61. PubMed ID: 18344013
[TBL] [Abstract][Full Text] [Related]
3. Screening using serum percentage of carbohydrate-deficient transferrin for congenital disorders of glycosylation in children with suspected metabolic disease.
Pérez-Cerdá C; Quelhas D; Vega AI; Ecay J; Vilarinho L; Ugarte M
Clin Chem; 2008 Jan; 54(1):93-100. PubMed ID: 18024528
[TBL] [Abstract][Full Text] [Related]
4. Transferrin D protein variants in the diagnosis of congenital disorders of glycosylation (CDG).
Marklová E; Albahri Z
J Clin Lab Anal; 2009; 23(2):77-81. PubMed ID: 19288450
[TBL] [Abstract][Full Text] [Related]
5. Isoelectric focusing with immobilized pH gradients for the analysis of transferrin (Tf) subtypes and variants.
Görg A; Weser J; Westermeier R; Postel W; Weidinger S; Patutschnick W; Cleve H
Hum Genet; 1983; 64(3):222-6. PubMed ID: 6885064
[TBL] [Abstract][Full Text] [Related]
6. Application of immobilized pH gradient isoelectric focusing to forensic hemogenetics: a survey on a three year experience with the transferrin (TF) and alpha 1-antitrypsin (PI) systems.
Skoda U; Fassbender L; Händler C; Mauff G; Pulverer G
Electrophoresis; 1988 Sep; 9(9):606-9. PubMed ID: 3266595
[TBL] [Abstract][Full Text] [Related]
7. Transferrin polymorphism detected in human urine using isoelectric focusing followed by immunoblotting.
Kishi K; Ikehara Y; Yasuda T; Mizuta K; Sato W
Forensic Sci Int; 1990 Apr; 45(3):225-30. PubMed ID: 2361645
[TBL] [Abstract][Full Text] [Related]
8. Ten years of screening for congenital disorders of glycosylation in Argentina: case studies and pitfalls.
Asteggiano CG; Papazoglu M; Bistué Millón MB; Peralta MF; Azar NB; Spécola NS; Guelbert N; Suldrup NS; Pereyra M; Dodelson de Kremer R
Pediatr Res; 2018 Dec; 84(6):837-841. PubMed ID: 30397276
[TBL] [Abstract][Full Text] [Related]
9. Fast screening of N-glycosylation disorders by sialotransferrin profiling with capillary zone electrophoresis.
Kingma HA; van der Sluijs FH; Heiner-Fokkema MR
Ann Clin Biochem; 2018 Nov; 55(6):693-701. PubMed ID: 29792046
[TBL] [Abstract][Full Text] [Related]
10. Transferrin (TF) polymorphism in Libyans.
Sebetan IM
Int J Legal Med; 1993; 106(1):51-2. PubMed ID: 8398892
[TBL] [Abstract][Full Text] [Related]
11. Our experience with diagnostics of congenital disorders of glycosylation.
Ziad A; Eliska M; Hubert V; Lenka M; Petr D; Sylva S; Marika T; Jaroslava V; Eva R
Acta Medica (Hradec Kralove); 2004; 47(4):267-72. PubMed ID: 15841907
[TBL] [Abstract][Full Text] [Related]
12. Improvement of CDG diagnosis by combined examination of several glycoproteins.
Fang J; Peters V; Assmann B; Körner C; Hoffmann GF
J Inherit Metab Dis; 2004; 27(5):581-90. PubMed ID: 15669673
[TBL] [Abstract][Full Text] [Related]
13. Transferrin variants in Tuscany (Italy). Evidence for two "new" Tf alleles.
Giari A; Weidinger S; Domenici R; Bargagna M
Hum Genet; 1985; 69(3):284-6. PubMed ID: 3980021
[TBL] [Abstract][Full Text] [Related]
14. Transferrin polymorphisms in Japanese populations: north-south cline in the distribution of the TF*C2 allele.
Nakanaga M; Yasuda T; Tenjo E; Nadano D; Fujiki N; Kishi K
Hum Biol; 1991 Apr; 63(2):186-95. PubMed ID: 2019411
[TBL] [Abstract][Full Text] [Related]
15. A transferrin D variant (DHR5) identical with DSaga by polyacrylamide gel isoelectric focusing was found in a disputed paternity case.
Ohshima T; Takayasu T; Umetsu K; Fujita M; Satoh C
Nihon Hoigaku Zasshi; 1998 Aug; 52(4):253-6. PubMed ID: 9893444
[TBL] [Abstract][Full Text] [Related]
16. Isoelectric focusing of rare transferrin (Tf) variants and common TfC subtypes.
Kühnl P; Spielmann W; Weber W
Hum Genet; 1979 Jan; 46(1):83-7. PubMed ID: 429010
[TBL] [Abstract][Full Text] [Related]
17. Congenital disorders of glycosylation.
Jaeken J
Ann N Y Acad Sci; 2010 Dec; 1214():190-8. PubMed ID: 21175687
[TBL] [Abstract][Full Text] [Related]
18. Genetic variability of transferrin subtypes in the populations of India.
Mastana SS; Papiha SS
Hum Biol; 1998 Aug; 70(4):729-44. PubMed ID: 9686483
[TBL] [Abstract][Full Text] [Related]
19. A novel mutation on the transferrin gene abolishes one N-glycosylation site and alters the pattern of transferrin isoforms, mimicking that observed after excessive alcohol consumption.
Grahn A; Bengtson P; Eklund E; Asin-Cayuela J
Clin Biochem; 2016 Apr; 49(6):511-513. PubMed ID: 26656560
[TBL] [Abstract][Full Text] [Related]
20. Identification of a new serum protein polymorphism as transferrin.
Thymann M
Hum Genet; 1978 Aug; 43(2):225-9. PubMed ID: 29004
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]