Detalhe da pesquisa
1.
Acute myeloid leukemia-induced functional inhibition of healthy CD34+ hematopoietic stem and progenitor cells.
Stem Cells
; 39(9): 1270-1284, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34013984
2.
Wilms' Tumor 1 Gene Expression Using a Standardized European LeukemiaNet-Certified Assay Compared to Other Methods for Detection of Minimal Residual Disease in Myelodysplastic Syndrome and Acute Myelogenous Leukemia after Allogeneic Blood Stem Cell Transplantation.
Biol Blood Marrow Transplant
; 24(11): 2337-2343, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29753838
3.
A novel inverted 17p13.3 microduplication disrupting PAFAH1B1 (LIS1) in a girl with syndromic lissencephaly.
Am J Med Genet A
; 161A(6): 1453-8, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23633430
4.
Recurrence and variability of germline EPCAM deletions in Lynch syndrome.
Hum Mutat
; 32(4): 407-14, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21309036
5.
Germline variants in DNA repair genes, including BRCA1/2, may cause familial myeloproliferative neoplasms.
Blood Adv
; 5(17): 3373-3376, 2021 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34477817
6.
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study.
BMC Gastroenterol
; 10: 112, 2010 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-20920174
7.
Improving the accuracy of prognostication in chronic myelomonocytic leukemia.
Expert Rev Anticancer Ther
; 20(8): 703-714, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32700646
8.
Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker.
Int J Cancer
; 124(7): 1727-35, 2009 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19115204
9.
MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases.
Hum Mutat
; 29(7): 948-58, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18431737
10.
Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC.
Eur J Hum Genet
; 16(7): 804-11, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18301449
11.
Invasive breast cancer cells exhibit increased mobility of the actin-binding protein CapG.
Int J Cancer
; 122(7): 1476-82, 2008 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18059028
12.
Efficacy of azacitidine is independent of molecular and clinical characteristics - an analysis of 128 patients with myelodysplastic syndromes or acute myeloid leukemia and a review of the literature.
Oncotarget
; 9(45): 27882-27894, 2018 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29963245
13.
Denaturing high-performance liquid chromatography (DHPLC) as a reliable high-throughput prescreening method for aberrant promoter methylation in cancer.
Hum Mutat
; 23(6): 612-20, 2004 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15146466
14.
Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin.
PLoS One
; 6(6): e20464, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21674048
15.
Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies.
Fam Cancer
; 10(2): 273-84, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21404117
16.
Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2.
J Cancer Res Clin Oncol
; 136(1): 123-34, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19669161
17.
Epigenetic silencing of the candidate tumor suppressor gene PROX1 in sporadic breast cancer.
Int J Cancer
; 121(3): 547-54, 2007 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17415710
18.
A novel mutation of the SGCE-gene in a German family with myoclonus-dystonia syndrome.
J Neurol
; 258(6): 1186-8, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21267590
19.
Delayed diagnosis and complications of Fanconi anaemia at advanced age--a paradigm.
Br J Haematol
; 133(2): 188-97, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16611311
20.
Systematic identification and molecular characterization of genes differentially expressed in breast and ovarian cancer.
J Pathol
; 205(1): 21-8, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15586368