E-LIB Suche - Ergebnisse für: Dogan, Muhammed Ensar

1

Gene variants of Congenital Adrenal Hyperplasia in Anatolia..:

Bayramov, Ruslan ; Dundar, Ayca ; Dogan, Muhammed Ensar...
Journal of Biotechnology. 280 (2018) - p. S21 , 2018

2

A case with 49, XXXXY syndrome: rare chromosomal aneuploidi..:

Erdogan, Murat ; Uzak, Asli Subasioglu ; Karabulut, Sevda Yesim...
Current Opinion in Biotechnology. 22 (2011) - p. S106 , 2011

Link: https://doi.org/10.1016/..

3

Pyruvate kinase deficiency in 29 Turkish patients with two ..:

Gök, Veysel ; Leblebisatan, Göksel ; Gürlek Gökçebay, Dilek...
British Journal of Haematology. , 2024

Link: https://doi.org/10.1111/..

4

EVs vs. EVs: MSCs and Tregs as a source of invisible possib..:

Heydari, Zahra ; Peshkova, Maria ; Gonen, Zeynep Burcin...
Journal of Molecular Medicine. 101 (2022) 1-2 - p. 51-63 , 2022

Link: https://doi.org/10.1007/..

5

A novel MTX2 gene splice site variant resulting in exon ski..:

Yeter Doğan, Burcu ; Günay, Neslihan ; Ada, Yasin.
American Journal of Medical Genetics Part A. 191 (2022) 1 - p. 173-182 , 2022

Link: https://doi.org/10.1002/..

6

Varied phenotypic spectrum presenting of paroxysmal exercis..:

Gultekin, Murat ; Dogan, Muhammet Ensar ; Simsir, Gulsah.
Neurological Sciences. 42 (2021) 11 - p. 4751-4754 , 2021

Link: https://doi.org/10.1007/..

7

A rare cause of membranoproliferative patterns of injury in..:

Günay, Neslihan ; Pınarbaşı, Ayşe Seda ; Doğan, Muhammet Ensar...
Pediatric Nephrology. 36 (2021) 12 - p. 4027-4028 , 2021

Link: https://doi.org/10.1007/..

8

A rare cause of membranoproliferative patterns of injury in..:

Günay, Neslihan ; Pınarbaşı, Ayşe Seda ; Doğan, Muhammet Ensar...
Pediatric Nephrology. 36 (2021) 12 - p. 4029-4032 , 2021

Link: https://doi.org/10.1007/..

9

Increased vitamin D receptor gene expression and rs11568820..:

Balta, Burhan ; Gumus, Hakan ; Bayramov, Ruslan...
Molecular Biology Reports. 45 (2018) 4 - p. 541-546 , 2018

Link: https://doi.org/10.1007/..

10

Two novel missense variants of FGFR2 gene in two patients w..:

Dogan, Muhammet Ensar ; Dundar, Bilge ; Gunes, Meltem Cerrah...
Journal of Biotechnology. 280 (2018) - p. S19-S20 , 2018

Link: https://doi.org/10.1016/..

11

NF1 gene variant allele frequencies comparison of Turkish p..:

Bayramov, Ruslan ; Dogan, Muhammet Ensar ; Gunes, Meltem Cerrah...
Journal of Biotechnology. 256 (2017) - p. S80 , 2017

Link: https://doi.org/10.1016/..

12

Frequency of chromosome variants in families with recurrent..:

Gunsili, Beyzanur ; Bayramov, Ruslan ; Kenanoglu, Sercan...
Journal of Biotechnology. 256 (2017) - p. S76 , 2017

Link: https://doi.org/10.1016/..

13

The correlation of genotype–phenotype of FMF disease and it..:

Yavuz, Fatih ; Bayramov, Ruslan ; Kenanoglu, Sercan...
Journal of Biotechnology. 256 (2017) - p. S75-S76 , 2017

Link: https://doi.org/10.1016/..

14

Retrospective results of 18 years prenatal diagnosis cases ..:

Bayramov, Ruslan ; Kutuk, Mehmet Serdar ; Kenanoglu, Sercan...
Journal of Biotechnology. 256 (2017) - p. S76 , 2017

Link: https://doi.org/10.1016/..

15

A novel nonsense mutation in GALNS gene in family with MPS4..:

Gunes, Meltem Cerrah ; Bayramov, Ruslan ; Boyukoglan, Ruksan...
Journal of Biotechnology. 231 (2016) - p. S108 , 2016

Link: https://doi.org/10.1016/..