Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 331

1.

c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia.

Ballmaier M, Germeshausen M, Schulze H, Cherkaoui K, Lang S, Gaudig A, Krukemeier S, Eilers M, Strauss G, Welte K.

Blood. 2001 Jan 1;97(1):139-46.

PMID:
11133753
[PubMed - indexed for MEDLINE]
Free Article
2.

[Congenital amegakaryocytic thrombocytopenia (CAMT) - a defect of the thrombopoietin receptor c-Mpl].

Germeshausen M, Schulze H, Gaudig A, Krukemeier S, Strauss G, Welte K, Ballmaier M.

Klin Padiatr. 2001 Jul-Aug;213(4):155-61. Review. German.

PMID:
11528548
[PubMed - indexed for MEDLINE]
3.

Implications of mutations in hematopoietic growth factor receptor genes in congenital cytopenias.

Germeshausen M, Ballmaier M, Welte K.

Ann N Y Acad Sci. 2001 Jun;938:305-20; discussion 320-1. Review.

PMID:
11458519
[PubMed - indexed for MEDLINE]
4.

Defective response to thrombopoietin and impaired expression of c-mpl mRNA of bone marrow cells in congenital amegakaryocytic thrombocytopenia.

Muraoka K, Ishii E, Tsuji K, Yamamoto S, Yamaguchi H, Hara T, Koga H, Nakahata T, Miyazaki S.

Br J Haematol. 1997 Feb;96(2):287-92.

PMID:
9029014
[PubMed - indexed for MEDLINE]
5.

MPL mutations in 23 patients suffering from congenital amegakaryocytic thrombocytopenia: the type of mutation predicts the course of the disease.

Germeshausen M, Ballmaier M, Welte K.

Hum Mutat. 2006 Mar;27(3):296.

PMID:
16470591
[PubMed - indexed for MEDLINE]
6.

Mutations in the thrombopoietin receptor, Mpl, in children with congenital amegakaryocytic thrombocytopenia.

van den Oudenrijn S, Bruin M, Folman CC, Peters M, Faulkner LB, de Haas M, von dem Borne AE.

Br J Haematol. 2000 Aug;110(2):441-8.

PMID:
10971406
[PubMed - indexed for MEDLINE]
7.

Thrombopoietin in patients with congenital thrombocytopenia and absent radii: elevated serum levels, normal receptor expression, but defective reactivity to thrombopoietin.

Ballmaier M, Schulze H, Strauss G, Cherkaoui K, Wittner N, Lynen S, Wolters S, Bogenberger J, Welte K.

Blood. 1997 Jul 15;90(2):612-9.

PMID:
9226161
[PubMed - indexed for MEDLINE]
Free Article
8.

Compound heterozygosity for two different amino-acid substitution mutations in the thrombopoietin receptor (c-mpl gene) in congenital amegakaryocytic thrombocytopenia (CAMT).

Tonelli R, Scardovi AL, Pession A, Strippoli P, Bonsi L, Vitale L, Prete A, Locatelli F, Bagnara GP, Paolucci G.

Hum Genet. 2000 Sep;107(3):225-33.

PMID:
11071383
[PubMed - indexed for MEDLINE]
9.

Functional analysis of single amino-acid mutations in the thrombopoietin-receptor Mpl underlying congenital amegakaryocytic thrombocytopenia.

Tijssen MR, di Summa F, van den Oudenrijn S, Zwaginga JJ, van der Schoot CE, Voermans C, de Haas M.

Br J Haematol. 2008 Jun;141(6):808-13. doi: 10.1111/j.1365-2141.2008.07139.x. Epub 2008 Apr 13.

PMID:
18422784
[PubMed - indexed for MEDLINE]
10.

Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome.

Letestu R, Vitrat N, Massé A, Le Couedic JP, Lazar V, Rameau P, Wendling F, Vuillier J, Boutard P, Plouvier E, Plasse M, Favier R, Vainchenker W, Debili N.

Blood. 2000 Mar 1;95(5):1633-41.

PMID:
10688818
[PubMed - indexed for MEDLINE]
Free Article
11.

Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations.

Savoia A, Dufour C, Locatelli F, Noris P, Ambaglio C, Rosti V, Zecca M, Ferrari S, di Bari F, Corcione A, Di Stazio M, Seri M, Balduini CL.

Haematologica. 2007 Sep;92(9):1186-93. Epub 2007 Aug 1.

PMID:
17666371
[PubMed - indexed for MEDLINE]
Free Article
12.

Deficiencies in progenitor cells of multiple hematopoietic lineages and defective megakaryocytopoiesis in mice lacking the thrombopoietic receptor c-Mpl.

Alexander WS, Roberts AW, Nicola NA, Li R, Metcalf D.

Blood. 1996 Mar 15;87(6):2162-70.

PMID:
8630375
[PubMed - indexed for MEDLINE]
Free Article
13.

[From gene to disease; from a thrombopoietin receptor gene defect to congenital amegakaryocytic thrombocytopenia].

van den Oudenrijn S, Bruin M, de Haas M, von dem Borne AE.

Ned Tijdschr Geneeskd. 2002 Mar 9;146(10):469-71. Dutch.

PMID:
11913111
[PubMed - indexed for MEDLINE]
14.

Identification of mutations in the c-mpl gene in congenital amegakaryocytic thrombocytopenia.

Ihara K, Ishii E, Eguchi M, Takada H, Suminoe A, Good RA, Hara T.

Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):3132-6.

PMID:
10077649
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Thrombopoietin is essential for the maintenance of normal hematopoiesis in humans: development of aplastic anemia in patients with congenital amegakaryocytic thrombocytopenia.

Ballmaier M, Germeshausen M, Krukemeier S, Welte K.

Ann N Y Acad Sci. 2003 May;996:17-25.

PMID:
12799278
[PubMed - indexed for MEDLINE]
16.

Three parameters, plasma thrombopoietin levels, plasma glycocalicin levels and megakaryocyte culture, distinguish between different causes of congenital thrombocytopenia.

van den Oudenrijn S, Bruin M, Folman CC, Bussel J, de Haas M, von dem Borne AE.

Br J Haematol. 2002 May;117(2):390-8.

PMID:
11972523
[PubMed - indexed for MEDLINE]
17.

Defective c-Mpl signaling in the syndrome of thrombocytopenia with absent radii.

Ballmaier M, Schulze H, Cremer M, Folman CC, Strauss G, Welte K.

Stem Cells. 1998;16 Suppl 2:177-84.

PMID:
11012189
[PubMed - indexed for MEDLINE]
Free Article
18.

Regulation of platelet activation in vitro by the c-Mpl ligand, thrombopoietin.

Chen J, Herceg-Harjacek L, Groopman JE, Grabarek J.

Blood. 1995 Dec 1;86(11):4054-62.

PMID:
7492761
[PubMed - indexed for MEDLINE]
Free Article
19.

Studies of the c-Mpl thrombopoietin receptor through gene disruption and activation.

Alexander WS, Roberts AW, Maurer AB, Nicola NA, Dunn AR, Metcalf D.

Stem Cells. 1996;14 Suppl 1:124-32. Review.

PMID:
11012212
[PubMed - indexed for MEDLINE]
Free Article
20.

Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation.

Heller PG, Glembotsky AC, Gandhi MJ, Cummings CL, Pirola CJ, Marta RF, Kornblihtt LI, Drachman JG, Molinas FC.

Blood. 2005 Jun 15;105(12):4664-70. Epub 2005 Mar 1.

PMID:
15741216
[PubMed - indexed for MEDLINE]
Free Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk