Detalhe da pesquisa
1.
Local Renin-Angiotensin system in normal hematopoietic and multiple myeloma-related progenitor cells.
Turk J Haematol
; 31(2): 136-42, 2014 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-25035670
2.
A new line method; A direct test in spinal muscular atrophy screening for DBS.
Mol Genet Genomic Med
; 11(12): e2270, 2023 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-37614112
3.
ABL gene kinase domain mutation scanning by denaturing high performance liquid chromatography sequencing method.
Turk J Haematol
; 28(2): 97-102, 2011 Jun 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27264123
4.
Minimal Residual Disease (MRD) Detection with Translocations and T-Cell Receptor and Immunoglobulin Gene Rearrangements in Adult Acute Lymphoblastic Leukaemia Patients: A Pilot Study.
Turk J Haematol
; 25(3): 124-32, 2008 Sep 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27264703
5.
Effect of carbapenems on the transcriptional expression of the oprD, oprM and oprN genes in Pseudomonas aeruginosa.
J Med Microbiol
; 53(Pt 9): 915-920, 2004 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-15314200
6.
Quantification of the FLI1 and CXCR4 gene expressions in acute lymphoblastic leukemia (ALL) patients with t(12,21).
Turk J Haematol
; 21(2): 87-92, 2004 Jun 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27263845
7.
Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia.
Leuk Res
; 36(1): 87-92, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-21813177
8.
Sequence variations of NKX2-5 and HAND1 genes in patients with atrial isomerism.
Anadolu Kardiyol Derg
; 11(4): 319-28, 2011 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-21561848
9.
Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL.
Dis Markers
; 28(6): 353-60, 2010.
Artigo
Inglês
| MEDLINE | ID: mdl-20683149
10.
1007fs, G908R, R702W mutations and P268S, IVS8+158 polymorphisms of the CARD15 gene in Turkish inflammatory bowel disease patients and their relationship with disease-related surgery.
Dig Dis Sci
; 53(6): 1683-92, 2008 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-17978873
11.
The SOCS-1 gene methylation in chronic myeloid leukemia patients.
Am J Hematol
; 82(8): 729-30, 2007 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-17315216
12.
HFE gene mutation, chronic liver disease, and iron overload In Turkey.
Dig Dis Sci
; 52(11): 3298-302, 2007 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-17410459
13.
Definition of C282Y mutation in a hereditary hemochromatosis family from Turkey.
Turk J Gastroenterol
; 18(1): 53-7, 2007 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-17450498
14.
Altered cyclin D1 genotype distribution in human sporadic pituitary adenomas.
Med Sci Monit
; 13(10): CR457-63, 2007 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-17901853
15.
Role of CYP2D6, CYP1A1, CYP2E1, GSTT1, and GSTM1 genes in the susceptibility to acute leukemias.
Am J Hematol
; 81(3): 162-70, 2006 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-16493615
16.
CYP2D6 and CYP1A1 mutations in the Turkish population.
Cell Biochem Funct
; 23(2): 133-5, 2005.
Artigo
Inglês
| MEDLINE | ID: mdl-15648054