174 related articles for article (PubMed ID: 9572993)
21. Linkage analysis of a large inbred family with congenital megaloblastic anemia.
Al-Alami JR; Tayeh MK; Al-Sheyyab MY; El-Shanti HI
Saudi Med J; 2002 Oct; 23(10):1251-6. PubMed ID: 12436132
[TBL] [Abstract][Full Text] [Related]
22. Selective intestinal cobalamin malabsorption with proteinuria (Imerslund-Gräsbeck syndrome) in juvenile Beagles.
Fyfe JC; Hemker SL; Venta PJ; Stebbing B; Giger U
J Vet Intern Med; 2014; 28(2):356-62. PubMed ID: 24433284
[TBL] [Abstract][Full Text] [Related]
23. [Selective vitamin B 12 malabsorption in a 19-year-old patient].
Walser A; Eigenmann H; Gut A
Schweiz Med Wochenschr; 1989 Jul; 119(30):1053-6. PubMed ID: 2552572
[TBL] [Abstract][Full Text] [Related]
24. Cubilin and megalin expression and their interaction in the rat intestine: effect of thyroidectomy.
Yammani RR; Seetharam S; Seetharam B
Am J Physiol Endocrinol Metab; 2001 Nov; 281(5):E900-7. PubMed ID: 11595644
[TBL] [Abstract][Full Text] [Related]
25. Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients.
Bouchlaka C; Maktouf C; Mahjoub B; Ayadi A; Sfar MT; Sioud M; Gueddich N; Belhadjali Z; Rebaï A; Abdelhak S; Dellagi K
J Hum Genet; 2007; 52(3):262-270. PubMed ID: 17285242
[TBL] [Abstract][Full Text] [Related]
26. Imerslund-Gräsbeck Syndrome in an Infant with a Novel Intronic Variant in the
Pacitto A; Prontera P; Stangoni G; Stefanelli M; Ceppi S; Cerri C; Gurdo G; Mencarelli A; Esposito S
Int J Mol Sci; 2019 Jan; 20(3):. PubMed ID: 30691194
[TBL] [Abstract][Full Text] [Related]
27. Cubilin, the Intrinsic Factor-Vitamin B12 Receptor in Development and Disease.
Kozyraki R; Cases O
Curr Med Chem; 2020; 27(19):3123-3150. PubMed ID: 30295181
[TBL] [Abstract][Full Text] [Related]
28. A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).
Owczarek-Lipska M; Jagannathan V; Drögemüller C; Lutz S; Glanemann B; Leeb T; Kook PH
PLoS One; 2013; 8(4):e61144. PubMed ID: 23613799
[TBL] [Abstract][Full Text] [Related]
29. Cubilin, the intrinsic factor-vitamin B12 receptor.
Kozyraki R; Verroust P; Cases O
Vitam Horm; 2022; 119():65-119. PubMed ID: 35337634
[TBL] [Abstract][Full Text] [Related]
30. Decreased affinity of urinary intrinsic factor-cobalamin receptor in a case of Gräsbeck-Imerslund syndrome.
Guéant JL; Chery C; Namour F; Aimone-Gastin I; Wustinger M
Gastroenterology; 1999 May; 116(5):1274-6. PubMed ID: 10220529
[No Abstract] [Full Text] [Related]
31. Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.
Aminoff M; Tahvanainen E; Gräsbeck R; Weissenbach J; Broch H; de la Chapelle A
Am J Hum Genet; 1995 Oct; 57(4):824-31. PubMed ID: 7573042
[TBL] [Abstract][Full Text] [Related]
32. Loss of albumin and megalin binding to renal cubilin in rats results in albuminuria after total body irradiation.
Yammani RR; Sharma M; Seetharam S; Moulder JE; Dahms NM; Seetharam B
Am J Physiol Regul Integr Comp Physiol; 2002 Aug; 283(2):R339-46. PubMed ID: 12121845
[TBL] [Abstract][Full Text] [Related]
33. Selective malabsorption of vitamin B12 and vitamin B12-intrinsic factor with megaloblastic anemia in an adult.
Chisholm JC
J Natl Med Assoc; 1985 Oct; 77(10):835-6, 838. PubMed ID: 4057272
[TBL] [Abstract][Full Text] [Related]
34. Proteinuria in cubilin-deficient patients with selective vitamin B12 malabsorption.
Wahlstedt-Fröberg V; Pettersson T; Aminoff M; Dugué B; Gräsbeck R
Pediatr Nephrol; 2003 May; 18(5):417-21. PubMed ID: 12687456
[TBL] [Abstract][Full Text] [Related]
35. Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7.
Namour F; Dobrovoljski G; Chery C; Audonnet S; Feillet F; Sperl W; Gueant JL
Haematologica; 2011 Nov; 96(11):1715-9. PubMed ID: 21750092
[TBL] [Abstract][Full Text] [Related]
36. [Imerslund-Gräsbeck's syndrome. Selective vitamin B12 malabsorption and proteinuria].
Scheibel E; Heilmann C; Hjelt K; Nielsen S
Ugeskr Laeger; 1981 Oct; 143(43):2818-9. PubMed ID: 7324233
[No Abstract] [Full Text] [Related]
37. New insights into carrier binding and epithelial uptake of the erythropoietic nutrients cobalamin and folate.
Moestrup SK
Curr Opin Hematol; 2006 May; 13(3):119-23. PubMed ID: 16567952
[TBL] [Abstract][Full Text] [Related]
38. Imerslund-Gräsbeck syndrome in a 15-year-old German girl caused by compound heterozygous mutations in CUBN.
Hauck FH; Tanner SM; Henker J; Laass MW
Eur J Pediatr; 2008 Jun; 167(6):671-5. PubMed ID: 17668238
[TBL] [Abstract][Full Text] [Related]
39. Molecular study of proteinuria in patients treated with B₁₂ supplements: do not forget megaloblastic anemia type 1.
Levin-Iaina N; Dinour D; Morduchowicz G; Ganon L; Holtzman EJ
Nephron Clin Pract; 2011; 118(2):c67-71. PubMed ID: 21150213
[TBL] [Abstract][Full Text] [Related]
40. Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo.
He Q; Madsen M; Kilkenney A; Gregory B; Christensen EI; Vorum H; Højrup P; Schäffer AA; Kirkness EF; Tanner SM; de la Chapelle A; Giger U; Moestrup SK; Fyfe JC
Blood; 2005 Aug; 106(4):1447-53. PubMed ID: 15845892
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
