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Molecular characterization of a case of atransferrinemia

Data up to Jan 2025

Published2000
Citations167
References21

Total Citations Per Year

Abstract

References (21)

Human Polymorphic Genes: World Distribution

1988 • 294 citations

The molecular defect in hypotransferrinemic mice

2000 • 177 citations

A Family of Congenital Atransferrinemia

1972 • 174 citations

Congenital Atransferrinemia A Case Report and Review of the Literature

1991 • 112 citations

A splicing defect in the mouse transferrin gene leads to congenital atransferrinemia

1989 • 107 citations

Importance of Anemia and Transferrin Levels in the Regulation of Intestinal Iron Absorption in Hypotransferrinemic Mice

1999 • 49 citations

Nucleotide sequence of porcine liver transferrin

1988 • 49 citations

Characterization of the Goat Lactoferrin cDNA: Assignment of the Relevant Locus to Bovine U12 Synteny Group

1994 • 46 citations

The Effect of Transferrin Polymorphisms on Iron Metabolism

1999 • 36 citations

The nucleotide sequence of rabbit liver transferrin cDNA

1991 • 35 citations

The cDNA sequence of horse transferrin

1993 • 32 citations

Transferrin-Immune Complex Disease

1977 • 30 citations

Rat mammary-gland transferrin: nucleotide sequence, phylogenetic analysis and glycan structure

1995 • 25 citations

[Hemoglobin-Zurich syndrome].

1961 • 14 citations

Purification, crystallization, and X-ray diffraction studies of lactotransferrin from buffalo colostrum

1992 • 13 citations

[Congenital atransferrinemia in a 11-month-old child].

1968 • 9 citations

Kongenitale Atransferrinämie

2008 • 6 citations

[Atransferrinemic nephrotic syndrome. Clinical contribution and etiopathogenetic evaluation].

1968 • 5 citations

[Iron overload in hereditary atransferrinemia].

1986 • 5 citations

[Congenital transferrin deficiency].

1971 • 4 citations

Deleted Work

1955 • 0 citations

Cited By (0)

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Molecular characterization of a case of atransferrinemia (2000) – Blood | Metascience Observatory Explorer