Works matching IS 11108630 AND DT 2020 AND VI 21 AND IP 1

Results: 77

Understanding the genetic determinant of severity in viral diseases: a case of SARS-Cov-2 infection.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00122-z

By:

Oladejo, Babayemi Olawale;
Adeboboye, Covenant Femi;
Adebolu, Tinuola Tokunbo

Publication type:

Article

The association between toll-like receptor 4 (TLR4) genotyping and the risk of epilepsy in children.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00102-3

By:

Abdelsalam, Maha;
Abd Elmagid, Dina Salama;
Magdy, Hend;
El-Sabbagh, Amr Mohamed;
Mostafa, Maged

Publication type:

Article

Association between ABO blood groups and susceptibility to COVID-19: profile of age and gender in Iraqi patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00115-y

By:

Ad'hiah, Ali H.;
Abdullah, Maha H.;
Alsudani, Mustafa Y.;
Shnawa, Rasool M. S.;
Al-Sa'ady, Ali J. R.;
Allami, Risala H.;
Misha'al, Khawla I.;
Jassim, Iftikhar A.;
Taqi, Estabraq A.

Publication type:

Article

Low iron mitigates viral survival: insights from evolution, genetics, and pandemics—a review of current hypothesis.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00114-z

By:

Menshawey, Rahma;
Menshawey, Esraa;
Alserr, Ayman H. K.;
Abdelmassih, Antoine Fakhry

Publication type:

Article

Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00091-3

By:

Agarwala, Swati;
Veerappa, Avinash M.;
Ramachandra, Nallur B.

Publication type:

Article

Late-onset multiple acyl-CoA dehydrogenase deficiency with breast cancer.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00121-0

By:

Pavithran, Keechilat;
Pachat, Divya;
Vijaykumar, Dehannathparambil Kottarathil

Publication type:

Article

Vici syndrome in an Egyptian infant: case report and differential diagnosis of inherited hypopigmented disorders.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00103-2

By:

Abd Elmaksoud, Marwa;
Abeesh, Aya Attya;
Pereira, Catarina;
El-Deeb, Marwa El-Saeed

Publication type:

Article

Integrative analysis of mRNA and miRNA sequencing data for gliomas of various grades.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00119-8

By:

Gvaldin, Dmitry Y.;
Pushkin, Anton A.;
Timoshkina, Nataliya N.;
Rostorguev, Eduard E.;
Nalgiev, Arbi M.;
Kit, Oleg I.

Publication type:

Article

Contributory role of SARS-CoV-2 genomic variations and life expectancy in COVID-19 transmission and low fatality rate in Africa.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00116-x

By:

Omotoso, Olabode E.

Publication type:

Article

Susceptibility role of soluble HLA-G and HLA-G 14-bp insertion/deletion polymorphism in inflammatory bowel disease.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00104-1

By:

Abdul-Hussein, Sarah S.;
Ali, Ekhlass N.;
Alkhalidi, Nawal M. F.;
Zaki, Neihaya H.;
Ad'hiah, Ali H.

Publication type:

Article

Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00090-4

By:

Eid, Ola M.;
Eid, Maha M.;
Abdelrahman, Amany H.;
Abdel kader, Rania M. A.;
Farid, Marwa;
Mahrous, Rana;
Mekkawy, Mona K.;
Kamel, Alaa K.;
Mazen, Inas;
El-Bassyouni, Hala T.

Publication type:

Article

Computational evaluation of potent 2-(1H-imidazol-2-yl) pyridine derivatives as potential V600E-BRAF inhibitors.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00111-2

By:

Umar, Abdullahi Bello;
Uzairu, Adamu;
Shallangwa, Gideon Adamu;
Uba, Sani

Publication type:

Article

Development of a simple method for the analysis of phenylalanine in dried blood spot using tandem mass spectrometry.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00100-5

By:

Gouda, Amr S.;
Nazim, Walaa S.

Publication type:

Article

Hepatoprotective effect of Moringa oleifera extract on TNF-α and TGF-β expression in acetaminophen-induced liver fibrosis in rats.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00106-z

By:

Aly, Omnia;
Abouelfadl, Dalia M.;
Shaker, Olfat G.;
Hegazy, Gehan A.;
Fayez, Ahmed M.;
Zaki, Hanan Hassan

Publication type:

Article

Detection of tmprss2-erg and tmprss2-egr1 gene fusion in prostate cancer from a Chinese population.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00092-2

By:

Xu, Changqing;
Luo, Jindan;
Wang, Mengmeng;
Wang, Yin;
Chen, Zhaojing;
Cao, Yifei;
Hong, Yu;
Xu, Xianrong;
Yang, Jun

Publication type:

Article

Association between genetic polymorphism of XRCC6 T-991C and risk of varicocele.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00118-9

By:

Namvaran, Mohammad Reza;
Beyzaei, Zahra;
Mokhtari, Mohammad Javad;
Geramizadeh, Bita

Publication type:

Article

Case report: Pitt-Hopkins like syndrome with CNTNAP2 mutation.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00113-0

By:

AlBaazi, Sawsan;
Shareef, Hula

Publication type:

Article

DNA integrity index as a potential molecular biomarker in colorectal cancer.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00082-4

By:

Salem, Ramy;
Ahmed, Rasha;
Shaheen, Karim;
Abdalmegeed, Mohammed;
Hassan, Heba

Publication type:

Article

In silico analysis of non-synonymous single nucleotide polymorphisms of human DEFB1 gene.

Published in:

2020

By:

Venkata Subbiah, Harini;
Ramesh Babu, Polani;
Subbiah, Usha

Publication type:

Editorial

COL1A1 polymorphism and neurological complications in pediatric acute lymphoblastic leukemia patients and their associations with altered bone mineral density.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00083-3

By:

Omran, Alaa A.;
Nageeb, Rania S.;
Nageeb, Ghada S.;
Yosif, Manal A.;
Mohammad, Yassir A.;
Ali, Alshimaa A.;
Atfy, Mervat;
Azmy, Taghreed M.;
Elsaid, Hanaa H.

Publication type:

Article

Extended blood group profiles for Malays, Chinese, and Indians in peninsular Malaysia.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00096-y

By:

Hajar, Che Ghazali Norul;
Zefarina, Zulkafli;
Md. Riffin, Nor Suhaila;
Tuan Mohammad, Tuan Hulwani;
Hassan, Mohd Nazri;
Poonachi, Prathapan;
Safuan, Sabreena;
ElGhazali, Gehad;
Chambers, Geoffrey Keith;
Edinur, Hisham Atan

Publication type:

Article

A high mannose concentration is well tolerated by colorectal adenocarcinoma and melanoma cells but toxic to normal human gingival fibroblast: an in vitro investigation.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00109-w

By:

Mazlan, Muhammad Alif;
Isa, Muhammad Lokman Md.;
Ibrahim, Moustafa

Publication type:

Article

Effect of folic acid on animal models, cell cultures, and human oral clefts: a literature review.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00108-x

By:

Bendahan, Zita C.;
Escobar, Lina M.;
Castellanos, Jaime E.;
González-Carrera, María C.

Publication type:

Article

An in silico LLPS perturbation approach in the design of a novel SARS-CoV-2 spike receptor-binding domain inhibitor.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00105-0

By:

Durojaye, Olanrewaju Ayodeji;
Sedzro, Divine Mensah;
Mushiana, Talifhani;
Uzoeto, Henrietta Onyinye;
Cosmas, Samuel;
Ajima, Judith Nnedimkpa;
Ibiang, Glory Omini

Publication type:

Article

Genotype association of IP6K3 gene with Hashimoto's thyroiditis in Algerian population (Aures region).

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00086-0

By:

Kherrour, Warda;
Kalicanin, Dean;
Brčić, Luka;
Hambaba, Leila;
Yahia, Mouloud;
Benbia, Souheyla;
Perica, Vesna Boraska

Publication type:

Article

Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotype.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00093-1

By:

El-Dessouky, Sara H.;
Hosny, Heba;
Elarab, Ahmed Ezz;
Issa, Mahmoud Y.

Publication type:

Article

Structure-based design of some quinazoline derivatives as epidermal growth factor receptor inhibitors.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00107-y

By:

Ibrahim, Muhammad Tukur;
Uzairu, Adamu;
Shallangwa, Gideon Adamu;
Uba, Sani

Publication type:

Article

Role of interleukins 12B and 17A genetic variation in house dust mites allergy.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00098-w

By:

Ammar, Asmaa Mostafa;
EL. Zayyat, Elham Abbas;
Khayyal, Amira EL. Saady;
Hamdy, Dina Mamdouh;
EL-Gendy, Aya;
Elleboudy, Noha Abdel Fattah

Publication type:

Article

Exploring the multiple roles of guardian of the genome: P53.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00089-x

By:

Feroz, Wasim;
Sheikh, Arwah Mohammad Ali

Publication type:

Article

Reductive regulation of BECN1 gene in adult Egyptian patients with do novo AML.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00087-z

By:

Ghozlan, Manal Fawzy;
Farweez, Botheina Ahmed Thabet;
Safwat, Nesma Ahmed;
Hassan, Noha Bassiouny;
Elsalakawy, Walaa Ali

Publication type:

Article

Genes predisposing to syndromic and nonsyndromic infertility: a narrative review.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00088-y

By:

Yahaya, Tajudeen O.;
Liman, Usman U.;
Abdullahi, Haliru;
Koko, Yahuza S.;
Ribah, Samuel S.;
Adamu, Zulkarnain;
Abubakar, Suleiman

Publication type:

Article

Evaluating of the association between ABO blood groups and coronavirus disease 2019 (COVID-19) in Iraqi patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00097-x

By:

Ad'hiah, Ali H.;
Allami, Risala H.;
Mohsin, Raghdan H.;
Abdullah, Maha H.;
AL-Sa'ady, Ali J. R.;
Alsudani, Mustafa Y.

Publication type:

Article

Prognostic significance of DNMT3a gene expression and reactive nitrogen species in newly diagnosed Egyptian de novo adult acute myeloid leukemia patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00066-4

By:

Asfour, Inas A.;
Hegab, Hany M.;
El-Salakawy, Walaa A.;
Hamza, Mohamed T.;
Mansour, Dina A.;
Saeed, Alia M.

Publication type:

Article

Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00101-4

By:

Gholipoorfeshkecheh, Rahim;
Agarwala, Swati;
G, Kavya;
Krishnappa, Santhosh;
Savitha, Mysore R.;
Ramachandra, Nallur B.

Publication type:

Article

Expression of miR-146a and miR-155 in Egyptian patients with Behçet's disease: clinical significance and relationship with disease activity.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00085-1

By:

El Khateeb, Engy;
Nassef, Ayatallah;
Gheith, Rasha;
Erfan, Aya;
Abdelfattah, Walaa

Publication type:

Article

Lysinuric protein intolerance: an overlooked diagnosis.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00084-2

By:

Olgac, Asburce;
Yenicesu, Idil;
Ozgul, Rıza Köksal;
Biberoğlu, Gürsel;
Tümer, Leyla

Publication type:

Article

Inherited thrombophilia and recurrent pregnancy loss: a single-center case-control study in North-Western Algeria.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00077-1

By:

Nassour-Mokhtari, Ilhem;
Loukidi, Bouchra;
Moussouni, Abdellatif;
Bettioui, Reda;
Benhabib, Riad;
Merzouk, Hafida;
Aouar, Amaria;
Allal-Taouli, Katia

Publication type:

Article

Potential therapeutic target identification in the novel 2019 coronavirus: insight from homology modeling and blind docking study.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00081-5

By:

Durojaye, Olanrewaju Ayodeji;
Mushiana, Talifhani;
Uzoeto, Henrietta Onyinye;
Cosmas, Samuel;
Udowo, Victor Malachy;
Osotuyi, Abayomi Gaius;
Ibiang, Glory Omini;
Gonlepa, Miapeh Kous

Publication type:

Article

The morbidity and mortality of COVID-19 are correlated with the Ile105Val glutathione S-transferase P1 polymorphism.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00094-0

By:

Saadat, Mostafa

Publication type:

Article

COVID-19 susceptibility: potential of ACE2 polymorphisms.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00099-9

By:

Chaudhary, Mayank

Publication type:

Article

Assessment of vitamin D-binding protein (DBP) gene polymorphisms and their correlation with multiple sclerosis: a case-control study in a sample of the Syrian population.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00076-2

By:

Alhomsi, Bushra;
Aboualchamat, Ghalia;
Alkadi, Imad

Publication type:

Article

Strategies to target long non-coding RNAs in cancer treatment: progress and challenges.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00074-4

By:

Fathi Dizaji, Behdokht

Publication type:

Article

Role of swimming on muscle PGC-1α, FNDC5 mRNA, and assessment of serum omentin, adropin, and irisin in high carbohydrate high fat (HCHF) diet induced obesity in rats.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00080-6

By:

Badawy, Ehsan;
El-laithy, Nabila A.;
Morsy, Safaa M.;
Ashour, Magdi N.;
Elias, Tahany R.;
Masoud, Mahmoud M.;
Aly, Omnia

Publication type:

Article

Prognostic value of CIP2A gene expression in adult Egyptian acute myeloid leukemia patients.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00075-3

By:

Shafik, Roxan E.;
Ibrahim, Azza M.;
Said, Fadwa;
Hassan, Naglaa M.;
Shafik, Hanan E.;
Shokralla, Hala A.

Publication type:

Article

Hematological and demographic profile of Pakistani children with isolated ventricular septal defects (VSDs).

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00079-z

By:

Sarwar, Sumbal;
Shabana;
Ehsan, Farah;
Tahir, Amna;
Jamil, Mahrukh;
Shahid, Saleem Ullah;
Hasnain, Shahida;
Khan, Asim;
Hyder, Syed Najam

Publication type:

Article

Evaluation of glutathione S-transferase polymorphism in Iranian patients with type 2 diabetic microangiopathy.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00078-0

By:

Hashemi-Soteh, Mohammad Bagher;
Ahmadzadeh Amiri, Amir;
Sheikh Rezaee, Majid Reza;
Ahmadzadeh Amiri, Ali;
Ahrari, Rohodin;
Ahmadzadeh Amiri, Ahmad;
Daneshvar, Fatemeh

Publication type:

Article

Clinical impact of early minimal residual disease detection at day 15 in precursor B-childhood acute lymphoblastic leukemia: an Egyptian experience.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00065-5

By:

Farweez, Botheina Ahmed Thabet;
Kassim, Nevine Ahmed;
Abdelfataah, Mona Fathy;
Hassan, Naglaa Mostafa;
Hassnien, Doha Elsayed Ahmed;
El-Sakhawy, Yasmin Nabil

Publication type:

Article

SHOX2 gene methylation in Egyptians having lung cancer.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00069-1

By:

Rizk, Mohamed Mostafa Mohamed Ahmed;
Helal, Suzan Mohamed Farouk;
Gad, Ahmed Youssef Shaaban;
Younan, Doreen Nazeih Assaad;
Moemen, Salma Abd El Maguid Mohamed Ramadan

Publication type:

Article

An in silico epitope-based peptide vaccine design against the 2019-nCoV.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00071-7

By:

Durojaye, Olanrewaju Ayodeji;
Mushiana, Talifhani;
Cosmas, Samuel;
Ibiang, Glory Omini;
Ibiang, Mercy Omini

Publication type:

Article

A novel mutation in ITGB4 gene in a newborn with epidermolysis bullosa, pyloric atresia, and aplasia cutis congenita.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-00055-7

By:

Okulu, Emel;
Durmaz, Ceren D.;
Tunc, Gaffari;
Guzel, Adil;
Kutlay, Nuket Y.;
Erdeve, Omer;
Atasay, Begum;
McGrath, John A.;
Liu, Lu;
Arsan, Saadet

Publication type:

Article