Detalles de la búsqueda
1.
Discovery of a novel homozygous SOD1 truncating variant bolsters infantile SOD1 deficiency syndrome.
Mol Biol Rep
; 51(1): 580, 2024 Apr 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-38668754
2.
Evaluation of the protective and therapeutic effects of extra virgin olive oil rich in phenol in experimental model of neonatal necrotizing enterocolitis by clinical disease score, inflammation, apoptosis, and oxidative stress markers.
Pediatr Surg Int
; 40(1): 80, 2024 Mar 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-38493431
3.
Evaluation of both expression and serum protein levels of caspase-8 and mitogen-activated protein kinase 1 genes in patients with different severities of COVID-19 infection.
Mol Biol Rep
; 50(4): 3241-3248, 2023 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-36708447
4.
The evaluation of both the expression and serum protein levels of Caspase-3 gene in patients with different degrees of SARS-CoV2 infection.
J Med Virol
; 94(3): 897-905, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34585746
5.
Study of ten causal genes in Turkish patients with clinically suspected maturity-onset diabetes of the young (MODY) using a targeted next-generation sequencing panel.
Mol Biol Rep
; 49(8): 7483-7495, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-35733065
6.
Expression of nucleolin, nucleophosmin, upstream binding transcription factor genes and propolis in wound models.
J Wound Care
; 31(Sup10): S28-S40, 2022 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36240873
7.
A novel pathogenic variant in the 3' end of the AGTPBP1 gene gives rise to neurodegeneration without cerebellar atrophy: an expansion of the disease phenotype?
Neurogenetics
; 22(2): 127-132, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33909173
8.
An integrated clinical and molecular study of a cohort of Turkish patients with Marfan syndrome harboring known and novel FBN1 variants.
J Hum Genet
; 66(7): 647-657, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-33483584
9.
Clinical, radiological and computational studies on two novel GNPTG variants causing mucolipidosis III gamma phenotypes with varying severity.
Mol Biol Rep
; 48(2): 1465-1474, 2021 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-33507475
10.
Clinical and molecular findings in a Turkish family with an ultra-rare condition, ELP2-related neurodevelopmental disorder.
Mol Biol Rep
; 48(1): 701-708, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-33393008
11.
May Argyrophilic Nucleolar Organizer Regions Be Used as a Biomarker for the Detection of the Degree of Ischemic Damage Instead of Tunel in Testicular Torsion?
Medicina (Kaunas)
; 57(11)2021 Oct 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-34833395
12.
Argyrophilic nucleolar organizer regions as a promising biomarker for the detection of brain hypoxia levels caused by different doses of carbon monoxide poisoning.
Gac Med Mex
; 157(6): 610-617, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-35108251
13.
Does capsaicin have therapeutic benefits in human colon adenocarcinoma? Selection of the most reliable dose via AgNOR
Turk J Med Sci
; 50(4): 1076-1081, 2020 06 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-32490651
14.
Argyrophilic nucleolar organizing regions in patients with Xeroderma Pigmentosum Group E.
Exp Dermatol
; 30(3): 416-417, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33200418
15.
Reduction of the argyrophilic nucleolar organizing region associated protein synthesis with age in buccal epithelial cells of healthy individuals.
Aging Clin Exp Res
; 27(2): 201-8, 2015 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-25082567
16.
Endothelial nitric oxide synthase gene polymorphisms (promoter -786T/C, exon 894 G/T and intron G10T) in unexplained female infertility.
Gynecol Obstet Invest
; 77(2): 89-93, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24504178
17.
Evaluation of smoking habits among Turkish family physicians.
Toxicol Ind Health
; 30(1): 3-11, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-22627461
18.
A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del).
Genes Genomics
; 46(5): 613-620, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38363456
19.
Radiosensitivity in a newborn with microcephalia: A case report of Nijmegen breakage syndrome.
Birth Defects Res
; 116(5): e2346, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38761025
20.
Investigation of MTHFR C677T gene polymorphism, biochemical and clinical parameters in Turkish migraine patients: association with allodynia and fatigue.
Cell Mol Neurobiol
; 33(8): 1055-63, 2013 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-23975093