Detalhe da pesquisa
1.
Glycosaminoglycan-induced proinflammatory cytokine levels as disease marker in mucopolysaccharidosis.
Cytokine
; 173: 156410, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37924740
2.
Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation.
Hemoglobin
; 47(4): 137-139, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37605549
3.
Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis.
Genet Med
; 24(10): 2187-2193, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35962790
4.
The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model.
Pediatr Res
; 90(3): 559-564, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33096541
5.
The association between genetic polymorphisms in matrix metalloproteinases and caries experience.
Clin Oral Investig
; 25(9): 5403-5410, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33638713
6.
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey
Turk J Med Sci
; 51(4): 1775-1780, 2021 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33581708
7.
Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice.
Mol Ther
; 27(12): 2123-2133, 2019 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31543414
8.
Propolis prevents inhibition of apoptosis by potassium bromate in CCD 841 human colon cell.
Cell Biochem Funct
; 38(4): 510-519, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31990996
9.
The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals.
Biol Sport
; 36(1): 9-16, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30899134
10.
Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis.
Genet Med
; 25(5): 100799, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36853234
11.
The missing "link": an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation.
Hum Genet
; 133(1): 29-39, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23982343
12.
A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome.
Hum Genet
; 132(11): 1311-20, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23851939
13.
The association of RANK gene C421T and C575T polymorphisms with bone mineral density in postmenopausal Turkish women.
Arch Gynecol Obstet
; 288(4): 917-23, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23553199
14.
Evaluation of IL-10, MCP-1, IFN gamma, and protectin D1 levels in patients with Hashimoto's thyroiditis.
Ir J Med Sci
; 192(1): 177-184, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36434424
15.
Clinicopathological characteristics, genetics and prognosis of patients with myeloid sarcoma: a single-center study.
J Clin Pathol
; 76(4): 244-251, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35927017
16.
The genotoxic effect of radiofrequency waves on mouse brain.
J Neurooncol
; 106(1): 53-8, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21732071
17.
Genotyping of ß-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders.
Hemoglobin
; 36(3): 230-43, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22524255
18.
Does the TMPRSS6 C > T Polymorphism Modify the Endurance Training Effects on Hematological Parameters?
Biol Trace Elem Res
; 200(6): 2588-2596, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34398419
19.
Acute hypoxia exposure following prenatal stress impairs hippocampus and novelty-seeking behavior in adolescent rats.
Int J Dev Neurosci
; 82(1): 85-95, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34850973
20.
Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patient.
Cancer Genet
; 266-267: 74-80, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35843036