about
Neurofibromatosis: novel and recurrent mutations in Turkish patientsHOXA11 and MMP2 gene expression in uterosacral ligaments of women with pelvic organ prolapse.BRCA1 and BRCA2 sequence variations detected with next-generation sequencing in patients with premature ovarian insufficiency.Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients.Coronin 1A inhibits neurite outgrowth in PC12 cells.FCN2 c.772G>T polymorphism is associated with chronic adenoiditis and/or tonsillitis, but not -4 A>G and -602 G>A.Retrieving relevant experiments: The case of microRNA microarrays.Thrombosis and risk factors: A comment.Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype.Biochemical, radiologic, ultrastructural, and genetic evaluation of iron overload in acute leukemia and iron-chelation therapy.Lack of association of matrix metalloproteinase-9 promoter gene polymorphism in obstructive sleep apnea syndrome.Enhancement of vascular endothelial growth factor's angiogenic capacity by the therapeutic modulation of notch signalling improves tram flap survival in rats submitted to nicotine.Vitamin D receptor gene TaqI single nucleotide polymorphism is not associated with lead levels in maternal and umbilical cord blood.The Impact of Iron Overload in Acute Leukemia: Chronic Inflammation, But Not the Presence of Nontransferrin Bound Iron is a Determinant of Oxidative Stress.Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype.The Notch pathway is a critical regulator of angiogenesis in a skin model of ischemia.Molecular genetic analyses in neurofibromatosis type 1 patients with tumors.Clinical findings and mutation analysis of NF1 patients in TurkeyThe Notch Signaling System Is Involved in the Regulation of Reparative Angiogenesis in the Zone of StasisChronic tonsillitis is not associated with beta defensin 1 gene polymorphisms in Turkish populationbeta-Adrenoreceptor antagonists reduce cancer cell proliferation, invasion, and migrationFractalkine receptor polymorphism and chronic tonsillitisNew Mutation Identified in the SRY Gene High Mobility Group (HMG)Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 geneA highly efficient and faithful MDS patient-derived xenotransplantation model for pre-clinical studiesThe differences in the expression of fractalkine and its receptor in conditions of tonsillar hypertrophy and chronic tonsillitis
P50
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description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Yunus K Terzi
@es
Yunus K. Terzi
@en
Yunus K. Terzi
@nl
Yunus K. Terzi
@sl
type
label
Yunus K Terzi
@es
Yunus K. Terzi
@en
Yunus K. Terzi
@nl
Yunus K. Terzi
@sl
altLabel
Yunus Kasim Terzi
@en
prefLabel
Yunus K Terzi
@es
Yunus K. Terzi
@en
Yunus K. Terzi
@nl
Yunus K. Terzi
@sl
P108
P106
P1153
11839698900
P21
P31
P496
0000-0001-5612-9696
P569
2000-01-01T00:00:00Z