Works in Egyptian Journal of Medical Human Genetics, 2017, Vol 18, Issue 4

Results: 15

Association assessment of platelet derived growth factor B gene polymorphism and its expression status with susceptibility to coronary artery disease.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 359, doi. 10.1016/j.ejmhg.2017.03.004

By:

Rezayani, Shayesteh;
Farazmandfar, Touraj;
shahbazi, Majid

Publication type:

Article

Identification of functional SNPs in human LGALS3 gene by in silico analyses.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 321, doi. 10.1016/j.ejmhg.2017.02.001

By:

Kaur, Tarnjeet;
Thakur, Kshema;
Singh, Jatinder;
Kamboj, Sukhdev Singh;
Kaur, Manpreet

Publication type:

Article

Extremely low frequency electromagnetic field in combination with β-Lapachone up-regulates the genes of non-homologous end joining.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 389, doi. 10.1016/j.ejmhg.2017.05.003

By:

Sanie-Jahromi, Fatemeh;
Mahmoudinasab, Hamideh;
Saadat, Mostafa

Publication type:

Article

Detection of Helicobacter pylori vacA, cagA and iceA1 virulence genes associated with gastric diseases in Egyptian patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 365, doi. 10.1016/j.ejmhg.2017.04.003

By:

El-Shenawy, Ahmed;
Diab, Manal;
Shemis, Mohamed;
El-Ghannam, Maged;
Salem, Dalia;
Abdelnasser, Moustafa;
Shahin, Mohamed;
Abdel-Hady, Mahmoud;
El-Sherbini, Effat;
Saber, Mohamed

Publication type:

Article

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II.

Published in:

2017

By:

Shawky, Rabah M.;
Gamal, Radwa;
Mohammad, Shaimaa Abdelsattar

Publication type:

Case Study

Open-array analysis of genetic variants in Egyptian patients with type 2 diabetes and obesity.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 341, doi. 10.1016/j.ejmhg.2017.03.002

By:

Attia, Hanaa R. M.;
Kamel, Solaf A.;
Ibrahim, Mona H.;
Farouk, Heba A.;
Rahman, Amany H. A.;
Sayed, Ghada H.;
Musa, Nevine I.

Publication type:

Article

Distribution of HLA-DRB1/DQB1 alleles and DRB1-DQB1 haplotypes among Tunisian patients with autoimmune hepatitis.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 335, doi. 10.1016/j.ejmhg.2017.02.003

By:

Chaouali, Marwa;
Kochkar, Radhia;
Messadi, Amira;
Tezeghdenti, Aymen;
Azaiez, Mouna Ben;
Abdallah, Hatem Ben;
Yacoubi-Oueslati, Basma;
Ghazouani, Ezzeddine

Publication type:

Article

Screening of polymorphisms in the folate pathway in Turkish pediatric Acute Lymphoblastic Leukemia patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 349, doi. 10.1016/j.ejmhg.2017.03.003

By:

Akin, Dilara Fatma;
Oner, Deniz Aslar;
Sipahi, Kadir;
Mumcuoglu, Mine;
Kurekci, Emin;
Ezer, Ustun;
Akar, Nejat

Publication type:

Article

Comparison of multiplex reverse transcription-PCR-enzyme hybridization assay with immunofluorescence techniques for the detection of four viral respiratory pathogens in pediatric community acquired pneumonia.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 355, doi. 10.1016/j.ejmhg.2017.04.001

By:

Mansour, Mervat Gamal Eldin;
Albendary, Sherin

Publication type:

Article

Germline variants in the ATM gene and breast cancer susceptibility in Moroccan women: A meta-analysis.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 329, doi. 10.1016/j.ejmhg.2017.02.002

By:

Marouf, Chaymaa;
Hajji, Omar;
Tazzite, Amal;
Jouhadi, Hassan;
Benider, Abdellatif;
Nadifi, Sellama

Publication type:

Article

Role of toll like receptors in bacterial and viral diseases -- A systemic approach.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 373, doi. 10.1016/j.ejmhg.2017.05.001

By:

Das, Avishek;
Guha, Pokhraj;
Sen, Debapriya;
Chaudhuri, Tapas Kumar

Publication type:

Article

Global distribution of consanguinity and their impact on complex diseases: Genetic disorders from an endogamous population.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 315, doi. 10.1016/j.ejmhg.2017.01.002

By:

Bener, Abdulbari;
Mohammad, Ramzi R.

Publication type:

Article

CYP2D6 pharmacogenomics.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 309, doi. 10.1016/j.ejmhg.2017.03.001

By:

Gopisankar, Mohanan Geetha

Publication type:

Article

A comparative study of mutation screening of sarcomeric genes (MYBPC3, MYH7, TNNT2) using single gene approach versus targeted gene panel next generation sequencing in a cohort of HCM patients in Egypt.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 381, doi. 10.1016/j.ejmhg.2017.05.002

By:

Kassem, Heba Sh.;
Walsh, Roddy;
Barton, Paul J.;
Abdelghany, Besra S.;
Azer, Remon S.;
Buchan, Rachel;
John, Shibu;
Elguindy, Ahmed;
Moharem-ElGamal, Sarah;
Badran, Hala M.;
Shehata, Hoda;
Cook, Stuart A.;
Yacoub, Magdi H.

Publication type:

Article

An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings.

Published in:

Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 4, p. 393, doi. 10.1016/j.ejmhg.2017.06.001

By:

Elsayed, Solaf M.;
Gamal, Radwa

Publication type:

Article