Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches von Shaik, Noor Ahmad, Nasser, Khalidah, Mohammed, Arif, Mujalli, Abdulrahman, Obaid, Ahmad A, El-Harouni, Ashraf A, Elango, Ramu, Banaganapalli, Babajan

Volltext

Pluripotent Stem Cell‐Derived Hematopoietic Progenitors Are Unable to Downregulate Key Epithelial‐Mesenchymal Transition‐Associated miRNAs von Meader, Ellie, Barta, Tomas, Melguizo‐Sanchis, Dario, Tilgner, Katarzyna, Montaner, David, El‐Harouni, Ashraf A., Armstrong, Lyle, Lako, Majlinda

Volltext

Distribution of CYP2C8 and CYP2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study von Rao, Durga Koteswara, Murthy, Dwaraknath K, Shaik, Nazia Sultana, Banaganapalli, Babajan, Konda, Kumaraswami, Rao, Hanmantha P, Ganti, Eswar, Ahmed Awan, Zuhair, A El‐Harouni, Ashraf, Elango, Ramu, Ali Khan, Imran, Shaik, Noor Ahmad

Volltext

iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors von Melguizo-Sanchis, Dario, Xu, Yaobo, Taheem, Dheraj, Yu, Min, Tilgner, Katarzyna, Barta, Tomas, Gassner, Katja, Anyfantis, George, Wan, Tengfei, Elango, Ramu, Alharthi, Sameer, El-Harouni, Ashraf A., Przyborski, Stefan, Adam, Soheir, Saretzki, Gabriele, Samarasinghe, Sujith, Armstrong, Lyle, Lako, Majlinda

Volltext

Review of literature: genes related to postaxial polydactyly von Verma, Prashant Kumar, El-Harouni, Ashraf A

Volltext

Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs) von Essawi, Mona L., Al-Attribi, Ghada M., Gaber, Khaled R., El-Harouni, Ashraf A.

Volltext

First Comprehensive In Silico Analysis of the Functional and Structural Consequences of SNPs in Human GalNAc-T1 Gene von Ali Mohamoud, Hussein Sheikh, Manwar Hussain, Muhammad Ramzan, El-Harouni, Ashraf A., Shaik, Noor Ahmad, Qasmi, Zaheer Ulhaq, Merican, Amir Feisal, Baig, Mukhtiar, Anwar, Yasir, Asfour, Hani, Bundajji, Nabil S., al-Aama, Jumana Yousuf

Volltext

Congenital heart defects in Down syndrome patients from western Saudi Arabia von AL-AAMA, Jumana Y, BONDAGJI, Nabeel S, EL-HAROUNI, Ashraf A

Volltext

Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches von Noor Ahmad Shaik, Khalidah Nasser, Arif Mohammed, Abdulrahman Mujalli, Ahmad A. Obaid, Ashraf A. El‐Harouni, Ramu Elango, Babajan Banaganapalli

Volltext

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery von Scott, Eric M, Halees, Anason, Itan, Yuval, Spencer, Emily G, He, Yupeng, Azab, Mostafa Abdellateef, Gabriel, Stacey B, Belkadi, Aziz, Boisson, Bertrand, Abel, Laurent, Clark, Andrew G, Alkuraya, Fowzan S, Casanova, Jean-Laurent, Gleeson, Joseph G

Volltext

Distribution of CYP 2C8 and CYP 2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study von Rao, Durga Koteswara, Murthy, Dwaraknath K, Shaik, Nazia Sultana, Banaganapalli, Babajan, Konda, Kumaraswami, Rao, Hanmantha P, Ganti, Eswar, Ahmed Awan, Zuhair, A El‐Harouni, Ashraf, Elango, Ramu, Ali Khan, Imran, Shaik, Noor Ahmad

Volltext

Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies von EFFAT, Laila K, EL-HAROUNI, Ashraf A, AMRA, Khalda S, EL-MINISI, Tarik I, MEGUID, Nagwa Abdel, EL-AWADY, Mostafa

Volltext

Exploring somatic mutations in BRAF , KRAS , and NRAS as therapeutic targets in Saudi colorectal cancer patients through massive parallel sequencing and variant classification von Aljuhani, Thamer Abdulhamid, Shaik, Noor Ahmad, Alqawas, Rahaf Talal, Bokhary, Rana Y, Al-Mutadares, Mahmood, Al Mahdi, Hadiah Bassam, Al-Rayes, Nuha, El-Harouni, Ashraf AbdulRahman, Elango, Ramu, Banaganapalli, Babajan, Awan, Zuhier Ahmad

Volltext

Structural characterization and conformational dynamics of alpha-1 antitrypsin pathogenic variants causing alpha-1-antitrypsin deficiency von Shaik, Noor Ahmad, Saud Al-Saud, Najla Bint, Abdulhamid Aljuhani, Thamer, Jamil, Kaiser, Alnuman, Huda, Aljeaid, Deema, Sultana, Nasreen, El-Harouni, Ashraf AbdulRahman, Awan, Zuhier Ahmed, Elango, Ramu, Banaganapalli, Babajan

Volltext

Review on Genes related to Postaxial Polydactyly von Ashraf AbdulRahman El-Harouni, Prashant Kumar Verma

Volltext