Computational Molecular Phenotypic Analysis of PTPN22 (W620R), IL6R (D358A), and TYK2 (P1104A) Gene Mutations of Rheumatoid Arthritis

Por Shaik, Noor Ahmad, Banaganapalli, Babajan
Publicado no Front Genet (2019)

Insights from Streptococcus pneumoniae glucose kinase structural model

Por Mulakayala, Chaitanya, Banaganapalli, Babajan Nawaz, Anuradha, CM, Chitta, Suresh Kumar
Publicado em 2009

Ursolic acid rich Ocimum sanctum L leaf extract loaded nanostructured lipid carriers ameliorate adjuvant induced arthritis in rats by inhibition of COX-1, COX-2, TNF-α and IL-1: Ph...

Por Ahmad, Aftab, Abuzinadah, Mohammed F., Alkreathy, Huda M., Banaganapalli, Babajan, Mujeeb, Mohd
Publicado no PLoS One (2018)

Design and evaluation of new chemotherapeutics of aloe-emodin (AE) against the deadly cancer disease: an in silico study

Por Mulakayala, Chaitanya, Banaganapalli, Babajan, Mulakayala, Naveen, Pulaganti, Madhusudana, C.M., Anuradha, Chitta, Suresh Kumar
Publicado em 2013

In-Silico Analysis of Inflammatory Bowel Disease (IBD) GWAS Loci to Novel Connections

Por Mesbah-Uddin, Md., Elango, Ramu, Banaganapalli, Babajan, Shaik, Noor Ahmad, Al-Abbasi, Fahad A.
Publicado no PLoS One (2015)

Computational Protein Phenotype Characterization of IL10RA Mutations Causative to Early Onset Inflammatory Bowel Disease (IBD)

Por Al-Abbasi, Fahad A., Mohammed, Kaleemuddin, Sadath, Saida, Banaganapalli, Babajan, Nasser, Khalidah, Shaik, Noor A.
Publicado no Front Genet (2018)

Molecular designing, virtual screening and docking study of novel curcumin analogue as mutation (S769L and K846R) selective inhibitor for EGFR

Por Shaik, Noor Ahmad, Al-Kreathy, Huda M., Ajabnoor, Ghada M., Verma, Prashant Kumar, Banaganapalli, Babajan
Publicado no Saudi J Biol Sci (2019)

Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients

Por Kamal, Naglaa M., Sahly, Ahmed N., Banaganapalli, Babajan, Rashidi, Omran M., Shetty, Preetha J., Al-Aama, Jumana Y., Shaik, Noor A., Elango, Ramu, Saadah, Omar I.
Publicado no Saudi J Biol Sci (2020)

Expanded Somatic Mutation Spectrum of MED12 Gene in Uterine Leiomyomas of Saudi Arabian Women

Por Ajabnoor, Ghada M. A., Mohammed, Nesma Amin, Banaganapalli, Babajan, Abdullah, Layla Saleh, Bondagji, Ola Nabeel, Mansouri, Nisma, Sahly, Nora Naif, Vaidyanathan, Venkatesh, Bondagji, Nabeel, Elango, Ramu, Shaik, Noor Ahmad
Publicado no Front Genet (2018)

Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis

Por Banaganapalli, Babajan, Mansour, Haifa, Mohammed, Arif, Alharthi, Arwa Mastoor, Aljuaid, Nada Mohammed, Nasser, Khalidah Khalid, Ahmad, Aftab, Saadah, Omar I., Al-Aama, Jumana Yousuf, Elango, Ramu, Shaik, Noor Ahmad
Publicado no Sci Rep (2020)

Identification of key regulatory genes connected to NF-κB family of proteins in visceral adipose tissues using gene expression and weighted protein interaction network

Por Sabir, Jamal S. M., El Omri, Abdelfatteh, Shaik, Noor A., Banaganapalli, Babajan, Al-Shaeri, Majed A., Alkenani, Naser A., Hajrah, Nahid H., Awan, Zuhier A., Zrelli, Houda, Elango, Ramu, Khan, Muhummadh
Publicado no PLoS One (2019)

Association of Four Missense SNPs with Preeclampsia in Saudi Women

Por Aljuaid, Nada Mohammed, Muharram, Ebtesam Ibrahim, Loqtum, Nouf Nasser, Al-Amoudi, Reem Mohammed, AlMahdi, Hadiah Bassam, Salama, Mohammed Assem, Banaganapalli, Babajan, Shaik, Noor Ahmad, Elango, Ramu, Bondagji, Nabeel Salem
Publicado no Saudi J Med Med Sci (2020)

Dissecting the Role of NF-κb Protein Family and Its Regulators in Rheumatoid Arthritis Using Weighted Gene Co-Expression Network

Por Sabir, Jamal S. M., El Omri, Abdelfatteh, Banaganapalli, Babajan, Al-Shaeri, Majed A., Alkenani, Naser A., Sabir, Mumdooh J., Hajrah, Nahid H., Zrelli, Houda, Ciesla, Lukasz, Nasser, Khalidah K., Elango, Ramu, Shaik, Noor Ahmad, Khan, Muhummadh
Publicado no Front Genet (2019)

Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients

Por Saadah, Omar I., Shaik, Noor Ahmad, Banaganapalli, Babajan, Salama, Mohammed A., Al-Harthi, Sameer E., Wang, Jun, Shawoosh, Harbi A., Alghamdi, Sharifa A., Bin-Taleb, Yagoub Y., Alhussaini, Bakr H., Elango, Ramu, Al-Aama, Jumana Y.
Publicado no Dis Markers (2015)

ACE insertion/deletion genetic polymorphism, serum ACE levels and high dietary salt intake influence the risk of obesity development among the Saudi adult population

Por Sabir, Jamal SM, Omri, Abdelfatteh El, Ali Khan, Imran, Banaganapalli, Babajan, Hajrah, Nahid H, Zrelli, Houda, Omar, Abdulkader M Shaikh, Alharbi, Mona G, Alhebshi, Alawiah M, Jansen, Robert K, Altaf, Abdulmalik, Shaik, Noor Ahmad, Khan, Muhummadh
Publicado no J Renin Angiotensin Aldosterone Syst (2019)

Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development among Saudi patients

Por Al-Aama, Jumana Yousuf, Shaik, Noor Ahmad, Banaganapalli, Babajan, Salama, Mohammed A., Rashidi, Omran, Sahly, Ahmed N., Mohsen, Mohammed O., Shawoosh, Harbi A., Shalabi, Hebah Ahmad, Edreesi, Mohammad Al, Alharthi, Sameer E., Wang, Jun, Elango, Ramu, Saadah, Omar I.
Publicado no PLoS One (2017)

The genetic association study of TP53 polymorphisms in Saudi obese patients

Por Sabir, Jamal S.M., El Omri, Abdelfatteh, Shaik, Noor A., Banaganapalli, Babajan, Hajrah, Nahid H., Zrelli, Houda, Arfaoui, Leila, Awan, Zuhier A., Shaikh Omar, Abdulkader M., Mohammed, Arif, Alharbi, Mona G., Alhebshi, Alawiah M., Jansen, Robert K., Khan, Muhummadh
Publicado no Saudi J Biol Sci (2019)

Unraveling the role of salt-sensitivity genes in obesity with integrated network biology and co-expression analysis

Por Sabir, Jamal Sabir M., El Omri, Abdelfatteh, Banaganapalli, Babajan, Aljuaid, Nada, Omar, Abdulkader M. Shaikh, Altaf, Abdulmalik, Hajrah, Nahid H., Zrelli, Houda, Arfaoui, Leila, Elango, Ramu, Alharbi, Mona G., Alhebshi, Alawiah M., Jansen, Robert K., Shaik, Noor A., Khan, Muhummadh
Publicado no PLoS One (2020)

Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease

Por Bokhari, Hifaa A., Shaik, Noor Ahmad, Banaganapalli, Babajan, Nasser, Khalidah Khalid, Ageel, Hossain Ibrahim, Al Shamrani, Ali Saad, Rashidi, Omran M., Al Ghubayshi, Omar Yaseen, Shaik, Jilani, Ahmad, Aftab, Alrayes, Nuha Mohammad, Al-Aama, Jumana Yousuf, Elango, Ramu, Saadah, Omar Ibrahim
Publicado no Saudi J Biol Sci (2020)

Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects

Por Gaboon, Nagwa E.A., Banaganapalli, Babajan, Nasser, Khalidah, Razeeth, Mohammed, Alsaedi, Mosab S., Rashidi, Omran M., Abdelwehab, Lereen S., Alahmadi, Turki Saad, Safdar, Osama Y., Shaik, Jilani, Choudhry, Hani M.Z., Al-numan, Huda Husain, Khan, Mohammad Imran, Al-Aama, Jumana Y., Elango, Ramu, Shaik, Noor A.
Publicado no Saudi J Biol Sci (2020)