Balkan Journal of Medical Genetics's Cover Image
Uneingeschränkter Zugang

Balkan Journal of Medical Genetics

Band 23 (2020): Heft 1 (Juni 2020)

COVER HERUNTERLADEN
Vorherige Ausgabe
Nächste Ausgabe
15 Artikel

Original Article

Uneingeschränkter Zugang | 26. Aug. 2020
Effect of exogenous transcription factors integration sites on safety and pluripotency of induced pluripotent stem cells
S Yin

S Yin

Department of Histoembryology, Genetics and Development, Shanghai Jiao Tong University School of MedicineShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Yin, S
, 
W Li

W Li

  • Shanghai Institute of Medical Genetics, Shanghai Children’s Hospital, Shanghai Jiao Tong UniversityShanghai, People’s Republic of China
  • National Health Commission Key Laboratory of Medical Embryogenesis and Developmental Molecular Biology & Shanghai Key Laboratory of Embryo and Reproduction EngineeringShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Li, W
, 
G Yang

G Yang

  • Shanghai Institute of Medical Genetics, Shanghai Children’s Hospital, Shanghai Jiao Tong UniversityShanghai, People’s Republic of China
  • National Health Commission Key Laboratory of Medical Embryogenesis and Developmental Molecular Biology & Shanghai Key Laboratory of Embryo and Reproduction EngineeringShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Yang, G
, 
Y Cheng

Y Cheng

  • Shanghai Institute of Medical Genetics, Shanghai Children’s Hospital, Shanghai Jiao Tong UniversityShanghai, People’s Republic of China
  • National Health Commission Key Laboratory of Medical Embryogenesis and Developmental Molecular Biology & Shanghai Key Laboratory of Embryo and Reproduction EngineeringShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Cheng, Y
, 
Q Yi

Q Yi

Department of Histoembryology, Genetics and Development, Shanghai Jiao Tong University School of MedicineShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Yi, Q
, 
S Fan

S Fan

  • Department of Histoembryology, Genetics and Development, Shanghai Jiao Tong University School of MedicineShanghai, People’s Republic of China
  • Shanghai Institute of Medical Genetics, Shanghai Children’s Hospital, Shanghai Jiao Tong UniversityShanghai, People’s Republic of China
  • National Health Commission Key Laboratory of Medical Embryogenesis and Developmental Molecular Biology & Shanghai Key Laboratory of Embryo and Reproduction EngineeringShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Fan, S
, 
Q Ma

Q Ma

  • Shanghai Institute of Medical Genetics, Shanghai Children’s Hospital, Shanghai Jiao Tong UniversityShanghai, People’s Republic of China
  • National Health Commission Key Laboratory of Medical Embryogenesis and Developmental Molecular Biology & Shanghai Key Laboratory of Embryo and Reproduction EngineeringShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Ma, Q
 und 
F Zeng

F Zeng

  • Department of Histoembryology, Genetics and Development, Shanghai Jiao Tong University School of MedicineShanghai, People’s Republic of China
  • Shanghai Institute of Medical Genetics, Shanghai Children’s Hospital, Shanghai Jiao Tong UniversityShanghai, People’s Republic of China
  • National Health Commission Key Laboratory of Medical Embryogenesis and Developmental Molecular Biology & Shanghai Key Laboratory of Embryo and Reproduction EngineeringShanghai, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Zeng, F
  
Uneingeschränkter Zugang | 26. Aug. 2020
Relationship between chromosomal aberrations and gene expressions in the p53 pathway in chronic lymphocytic leukemia
G Öztan

G Öztan

Division of Medical Genetics, Istanbul Faculty of Medicine, Istanbul Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Öztan, G
, 
M Aktan

M Aktan

Department of Internal Medicine, Division of Hematology, İstanbul University Faculty of Medicineİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Aktan, M
, 
S Palanduz

S Palanduz

Division of Medical Genetics, Istanbul Faculty of Medicine, Istanbul Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Palanduz, S
, 
H İşsever

H İşsever

Department of Public Health, İstanbul University Faculty of Medicineİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
İşsever, H
, 
S Öztürk

S Öztürk

Division of Medical Genetics, Istanbul Faculty of Medicine, Istanbul Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Öztürk, S
, 
E Nikerel

E Nikerel

Department of Genetics and Bioengineering, Yeditepe Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Nikerel, E
, 
A Uçur

A Uçur

Division of Medical Genetics, Istanbul Faculty of Medicine, Istanbul Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Uçur, A
, 
G Bağatir

G Bağatir

Division of Medical Genetics, Istanbul Faculty of Medicine, Istanbul Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Bağatir, G
, 
A Bayrak

A Bayrak

Division of Medical Genetics, Istanbul Faculty of Medicine, Istanbul Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Bayrak, A
 und 
K Çefle

K Çefle

Division of Medical Genetics, Istanbul Faculty of Medicine, Istanbul Universityİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Çefle, K
  
Uneingeschränkter Zugang | 26. Aug. 2020
The expression levels of microRNAs associated with T and B cell differentiation/stimulation in ankylosing spondylitis
A Türkyilmaz

A Türkyilmaz

Department of Medical Genetics, Marmara University School of Medicineİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Türkyilmaz, A
, 
P Ata

P Ata

Department of Medical Genetics, Marmara University School of Medicineİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Ata, P
, 
F Akbaş

F Akbaş

Department of Physical Theraphy and Rehabilitation, Marmara University School of Medicineİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Akbaş, F
 und 
İ Yağci

İ Yağci

Department of Physical Theraphy and Rehabilitation, Marmara University School of Medicineİstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Yağci, İ
  
Uneingeschränkter Zugang | 26. Aug. 2020
The effects of O6-methyl guanine DNA-methyl transferase promotor methylation and CpG1, CpG2, CpG3 and CpG4 methylation on treatment response and their prognostic significance in patients with glioblastoma
OG Yildiz

OG Yildiz

Department of Radiation Oncology, Erciyes University, School of MedicineKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Yildiz, OG
, 
D Aslan

D Aslan

Department of Radiation Oncology, Erciyes University, School of MedicineKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Aslan, D
, 
H Akalin

H Akalin

Department of Medical Genetics, Erciyes University, School of MedicineKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Akalin, H
, 
Y Erdem

Y Erdem

Department of Basic Pharmaceutical Sciences, Erciyes University, School of Pharmaceutical ScienceKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Erdem, Y
, 
O Canoz

O Canoz

Department of Pathology, School of Medicine, Erciyes UniversityKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Canoz, O
, 
A Aytekin

A Aytekin

Department of Radiation Oncology, Kayseri Training and Research HospitalKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Aytekin, A
, 
S Ozoner

S Ozoner

Department of Radiation Oncology, Erciyes University, School of MedicineKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Ozoner, S
 und 
M Dundar

M Dundar

Department of Medical Genetics, Erciyes University, School of MedicineKayseri, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Dundar, M
  
Uneingeschränkter Zugang | 26. Aug. 2020
β-Elemene inhibits the proliferation and migration of human glioblastoma cell lines via suppressing ring finger protein 135
M Alizada

M Alizada

Department of Neurosurgery, The First Affiliated Hospital of Dalian Medical UniversityDalian, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Alizada, M
, 
J Li

J Li

Department of Neurosurgery, The First Affiliated Hospital of Dalian Medical UniversityDalian, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Li, J
, 
H Aslami

H Aslami

Department of General Surgery, The First Affiliated Hospital of Dalian Medical UniversityDalian, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Aslami, H
, 
D Yang

D Yang

Department of Orthopedics, The First Affiliated Hospital of China Medical UniversityShenyang, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Yang, D
, 
T Korchuganova

T Korchuganova

Department of Plastic and Cosmetic surgery, The First Affiliated Hospital of Dalian Medical UniversityDalian, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Korchuganova, T
 und 
YH Xu

YH Xu

Department of Neurosurgery, The First Affiliated Hospital of Dalian Medical UniversityDalian, People’s Republic of China
Suche nach diesem Autor auf
Sciendo|Google Scholar
Xu, YH
  
Uneingeschränkter Zugang | 26. Aug. 2020
RANKL is a new epigenetic biomarker for the vasomotor symptom during Menopause
R Kalkan

R Kalkan

  • Department of Medical Genetics, Faculty of Medicine, Near East UniversityNicosia, Turkish Republic of Northern Cyprus
  • Experimental Health Sciences Research Center (DESAM), Near East UniversityNicosia, Turkish Republic of Northern Cyprus
Suche nach diesem Autor auf
Sciendo|Google Scholar
Kalkan, R
, 
M Altarda

M Altarda

Department of Medical Genetics, Faculty of Medicine, Near East UniversityNicosia, Turkish Republic of Northern Cyprus
Suche nach diesem Autor auf
Sciendo|Google Scholar
Altarda, M
 und 
O Tosun

O Tosun

Department of Biostatistics, Faculty of Medicine, Near East UniversityNicosia, Turkish Republic of Northern Cyprus
Suche nach diesem Autor auf
Sciendo|Google Scholar
Tosun, O
  
Uneingeschränkter Zugang | 26. Aug. 2020
The interaction of female age and active male smoking has negative influence on success rates of the in vitro fertilization treatments
E Petanovska Kostova

E Petanovska Kostova

In Vitro Fertilisation Centre, First Private General Hospital ReMedikaSkopje, North Macedonia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Petanovska Kostova, E
  
Uneingeschränkter Zugang | 26. Aug. 2020
An investigation of the COMT gene Val158Met polymorphism in patients admitted to the emergency department because of synthetic cannabinoid use
Y Nennicioglu

Y Nennicioglu

Emergency Department, Nusaybin Goverment Hospital, Emergency ServiceMardin, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Nennicioglu, Y
, 
H Kaya

H Kaya

Emergency Department, Science Health University, Yuksek Ihtisas Research and Education HospitalBursa, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Kaya, H
, 
S Eraybar

S Eraybar

Emergency Department, Science Health University, Yuksek Ihtisas Research and Education HospitalBursa, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Eraybar, S
, 
S Atmaca

S Atmaca

Emergency Department, Science Health University, Yuksek Ihtisas Research and Education HospitalBursa, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Atmaca, S
, 
O Gorukmez

O Gorukmez

Medical Genetics Department, Science Health University, Yuksek Ihtisas Research and Education HospitalBursa, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Gorukmez, O
 und 
E Armagan

E Armagan

Emergency Department, Uludag University Faculty of Medicine, Emergency DepartmentBursa, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Armagan, E
  
Uneingeschränkter Zugang | 26. Aug. 2020
Implication of VDR rs7975232 and FCGR2A rs1801274 gene polymorphisms in the risk and the prognosis of autoimmune thyroid diseases in the Tunisian population
S Mestiri

S Mestiri

Laboratory of Genetics, Biodiversity and Bioresource Valorization, Superior Institute of Biotechnology of Monastir, University of MonastirMonastir, Tunisia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Mestiri, S
, 
I Zaaber

I Zaaber

Laboratory of Genetics, Biodiversity and Bioresource Valorization, Superior Institute of Biotechnology of Monastir, University of MonastirMonastir, Tunisia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Zaaber, I
, 
I Nasr

I Nasr

Laboratory of Genetics, Biodiversity and Bioresource Valorization, Superior Institute of Biotechnology of Monastir, University of MonastirMonastir, Tunisia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Nasr, I
 und 
H Marmouch

H Marmouch

Department of Internal Medicine-Endocrinology, Hospital Fattouma BourguibaMonastir, Tunisia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Marmouch, H
  
Uneingeschränkter Zugang | 26. Aug. 2020
Association of the brain-derived neurotrophic factor Val66Met polymorphism with body mass index, fasting glucose levels and lipid status in adolescents
V Vidović

V Vidović

Department of Human Genetics, Faculty of Medicine, University of Banja LukaBanja Luka, Bosnia and Herzegovina
Suche nach diesem Autor auf
Sciendo|Google Scholar
Vidović, V
, 
N Maksimović

N Maksimović

Institute of Human Genetics, Faculty of Medicine, University of BelgradeBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Maksimović, N
, 
I Novaković

I Novaković

Institute of Human Genetics, Faculty of Medicine, University of BelgradeBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Novaković, I
, 
T Damnjanović

T Damnjanović

Institute of Human Genetics, Faculty of Medicine, University of BelgradeBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Damnjanović, T
, 
B Jekić

B Jekić

Institute of Human Genetics, Faculty of Medicine, University of BelgradeBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Jekić, B
, 
S Vidović

S Vidović

Department of Human Genetics, Faculty of Medicine, University of Banja LukaBanja Luka, Bosnia and Herzegovina
Suche nach diesem Autor auf
Sciendo|Google Scholar
Vidović, S
, 
N Majkić Singh

N Majkić Singh

Society of Medical BiochemistsBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Majkić Singh, N
, 
M Stamenković-Radak

M Stamenković-Radak

Department of Genetics and Evolution, Faculty of Biology, University of BelgradeBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Stamenković-Radak, M
, 
D Nikolić

D Nikolić

Department of Physical Medicine and Rehabilitation, Faculty of Medicine, University of Belgrade, University Children’s HospitalBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Nikolić, D
 und 
D Marisavljević

D Marisavljević

Department of Hematology, Medical Center Beza-nijska Kosa, Faculty of Medicine, University of BelgradeBelgrade, Serbia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Marisavljević, D
  

Case Report

Uneingeschränkter Zugang | 26. Aug. 2020
De novo KMT2D heterozygous frameshift deletion in a newborn with a congenital heart anomaly
Š Stangler Herodež

Š Stangler Herodež

  • Laboratory of Medical Genetics, University Medical Centre MariborMaribor, Slovenia
  • Medical Faculty, University of MariborMaribor, Slovenia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Stangler Herodež, Š
, 
N Marčun Varda

N Marčun Varda

  • Medical Faculty, University of MariborMaribor, Slovenia
  • Division of Paediatrics, University Medical Centre MariborMaribor, Slovenia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Marčun Varda, N
, 
Kokalj Vokač N

Kokalj Vokač N

  • Laboratory of Medical Genetics, University Medical Centre MariborMaribor, Slovenia
  • Medical Faculty, University of MariborMaribor, Slovenia
Suche nach diesem Autor auf
Sciendo|Google Scholar
N, Kokalj Vokač
 und 
D Krgović

D Krgović

  • Laboratory of Medical Genetics, University Medical Centre MariborMaribor, Slovenia
  • Medical Faculty, University of MariborMaribor, Slovenia
Suche nach diesem Autor auf
Sciendo|Google Scholar
Krgović, D
  
Uneingeschränkter Zugang | 26. Aug. 2020
A new splice-site mutation of SPINK5 gene in the Netherton syndrome with different clinical features: A case report
E Erden

E Erden

Department of Dermatology and Venereology, Yıldırım Beyazit UniversityAnkara, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Erden, E
, 
AC Ceylan

AC Ceylan

Department of Medical Genetics, Ankara City HospitalAnkara, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Ceylan, AC
 und 
S Emre

S Emre

Department of Dermatology and Venereology, Yıldırım Beyazit UniversityAnkara, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Emre, S
  
Uneingeschränkter Zugang | 26. Aug. 2020
Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene
M Tajir

M Tajir

  • Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed VRabat, Morocco
  • Department of Medical Genetics, National Institute of HealthRabat, Morocco
  • Medical Genetics Laboratory, Faculty of Medicine and Pharmacy, Mohamed Premier UniversityOujda, Morocco
Suche nach diesem Autor auf
Sciendo|Google Scholar
Tajir, M
, 
J Lyahyai

J Lyahyai

  • Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed VRabat, Morocco
  • Department of Medical Genetics, National Institute of HealthRabat, Morocco
Suche nach diesem Autor auf
Sciendo|Google Scholar
Lyahyai, J
, 
S Guaoua

S Guaoua

  • Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed VRabat, Morocco
  • Department of Medical Genetics, National Institute of HealthRabat, Morocco
Suche nach diesem Autor auf
Sciendo|Google Scholar
Guaoua, S
, 
M El Alloussi

M El Alloussi

Department of Pediatric Dentistry-Prevention, Faculty of Dental Medicine, Mohamed V Souissi UniversityRabat, Morocco
Suche nach diesem Autor auf
Sciendo|Google Scholar
El Alloussi, M
 und 
A Sefiani

A Sefiani

  • Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed VRabat, Morocco
  • Department of Medical Genetics, National Institute of HealthRabat, Morocco
Suche nach diesem Autor auf
Sciendo|Google Scholar
Sefiani, A
  
Uneingeschränkter Zugang | 26. Aug. 2020
Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report
A Karaman

A Karaman

Genetics Diagnosis Center, University of Health Sciences, Zeynep Kamil Women and Children Training and Research HospitalIstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Karaman, A
, 
B Karaman

B Karaman

Department of Medical Genetics, Istanbul University, Istanbul Faculty of MedicineIstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Karaman, B
, 
A Çetinkaya

A Çetinkaya

  • Genetics Diagnosis Center, University of Health Sciences, Zeynep Kamil Women and Children Training and Research HospitalIstanbul, Turkey
  • Department of Medical Genetics, Hacetepe University, Faculty of MedicineAnkara, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Çetinkaya, A
, 
S Karaman

S Karaman

Department of Anesthesia and Reanimation, University of Health Sciences Ümraniye Training and Research HospitalIstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Karaman, S
 und 
O Demirci

O Demirci

Perinatalogy Unit, University of Health Sciences Zeynep Kamil Women and Children Training and Research HospitalIstanbul, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Demirci, O
  
Uneingeschränkter Zugang | 26. Aug. 2020
A very rare partial trisomy syndrome: De novo duplication of 16q12.1q23.3 in a Turkish girl with developmental delay and facial dysmorphic features
A Türkyılmaz

A Türkyılmaz

Department of Medical Genetics, Erzurum Region Training and Research Hospital, Department of Medical GeneticsErzurum, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Türkyılmaz, A
 und 
O Yaralı

O Yaralı

Department of Medical Genetics, Erzurum Region Training and Research Hospital, Department of Medical GeneticsErzurum, Turkey
Suche nach diesem Autor auf
Sciendo|Google Scholar
Yaralı, O
  

Suche

Alle Bände und Hefte dieser Zeitschrift

Sprache:
Englisch
Zeitrahmen der Veröffentlichung:
2 Hefte pro Jahr
Fachgebiete der Zeitschrift:
Medizin, Vorklinische Medizin, Grundlagenmedizin, Vorklinische Medizin, Grundlagenmedizin, andere
Zeitschrift RSS Feed