Detalhe da pesquisa
1.
Deciphering the host genetic factors conferring susceptibility to severe COVID-19 using exome sequencing.
Genes Immun
; 25(1): 14-42, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38123822
2.
Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients.
J Clin Lab Anal
; 38(1-2): e24997, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38115218
3.
PPM1K defects cause mild maple syrup urine disease: The second case in the literature.
Am J Med Genet A
; 191(5): 1360-1365, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36706222
4.
Safety and efficacy of mesenchymal stromal cell therapy for multi-drug-resistant acute and late-acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation.
Ann Hematol
; 102(6): 1537-1547, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37067556
5.
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Funct Integr Genomics
; 22(3): 291-315, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35098403
6.
Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder.
Int J Neurosci
; 132(11): 1072-1079, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33287601
7.
Change in gene expression levels of GABA, glutamate and neurosteroid pathways due to acoustic trauma in the cochlea.
J Neurogenet
; 35(1): 45-57, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33825593
8.
Intralesional allogeneic adipose-derived stem cells application in chronic diabetic foot ulcer: Phase I/2 safety study.
Foot Ankle Surg
; 27(6): 636-642, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32826167
9.
The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.
Mol Biol Rep
; 46(4): 3677-3690, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31006099
10.
Assessment of genes involved in behavior, learning, memory, and synaptic plasticity following status epilepticus in rats.
Epilepsy Behav
; 98(Pt A): 101-109, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31326869
11.
A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant.
Pediatr Hematol Oncol
; 41(4): 301-309, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38047450
12.
Serum micro-rna profiles in patients with autosomal dominant polycystic kidney disease according to hypertension and renal function.
BMC Nephrol
; 18(1): 179, 2017 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28558802
13.
The Impact of Epigenetics on Mesenchymal Stem Cell Biology.
J Cell Physiol
; 231(11): 2393-401, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26960183
14.
Anthrax lethal factor as an immune target in humans and transgenic mice and the impact of HLA polymorphism on CD4+ T cell immunity.
PLoS Pathog
; 10(5): e1004085, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24788397
15.
The roles of CC2D1A and HTR1A gene expressions in autism spectrum disorders.
Metab Brain Dis
; 31(3): 613-9, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26782176
16.
[Identification of Mycobacterium species from BACTEC MGIT™ positive cultures with Oligo-FISH and PNA-FISH methods]. / BACTEC MGIT™ Pozitif Kültürlerden Mycobacterium türlerinin Oligo-FISH ve PNA-FISH Yöntemleriyle Tanimlanmasi.
Mikrobiyol Bul
; 48(3): 385-401, 2014 Jul.
Artigo
em Turco
| MEDLINE | ID: mdl-25052105
17.
ABCA4 variant screening in a Turkish cohort with Stargardt disease.
Ophthalmic Genet
; 45(2): 133-139, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38369462
18.
Trans Species RNA Activity: Sperm RNA of the Father of an Autistic Child Programs Glial Cells and Behavioral Disorders in Mice.
Biomolecules
; 14(2)2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38397438
19.
From Data to Insights: Machine Learning Empowers Prognostic Biomarker Prediction in Autism.
J Pers Med
; 13(12)2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38138941
20.
A Case of Short Stature Caused by a Mutation in the ACAN Gene.
Mol Syndromol
; 14(2): 123-128, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37064332