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

por Shaik, Noor Ahmad, Banaganapalli, Babajan
Publicado en Front Genet (2019)

Insights from Streptococcus pneumoniae glucose kinase structural model

por Mulakayala, Chaitanya, Banaganapalli, Babajan Nawaz, Anuradha, CM, Chitta, Suresh Kumar
Publicado 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 en 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 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 en 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 en 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 en Saudi J Biol Sci (2019)

Multilevel systems biology analysis of lung transcriptomics data identifies key miRNAs and potential miRNA target genes for SARS-CoV-2 infection

por Banaganapalli, Babajan, Al-Rayes, Nuha, Awan, Zuhier Ahmed, Alsulaimany, Faten A., Alamri, Abdulhakeem S., Elango, Ramu, Malik, Md Zubbair, Shaik, Noor A.
Publicado en Comput Biol Med (2021)

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 en Saudi J Biol Sci (2020)

Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen

por Awan, Zuhier Ahmed, Rashidi, Omran M., Al-Shehri, Bandar Ali, Jamil, Kaiser, Elango, Ramu, Al-Aama, Jumana Y., Hegele, Robert A., Banaganapalli, Babajan, Shaik, Noor A.
Publicado en Front Med (Lausanne) (2021)

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 en 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 en 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 en 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 en Saudi J Med Med Sci (2020)

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

por Saadah, Omar I., Banaganapalli, Babajan, Kamal, Naglaa M., Sahly, Ahmed N., Alsufyani, Hadeel A., Mohammed, Arif, Ahmad, Aftab, Nasser, Khalidah Khalid, Al-Aama, Jumana Y., Shaik, Noor Ahmad, Elango, Ramu
Publicado en Front Pediatr (2021)

TagSNP approach for HLA risk allele genotyping of Saudi celiac disease patients: effectiveness and pitfalls

por Baaqeel, Reham H., Banaganapalli, Babajan, Al Mahdi, Hadiah Bassam, Salama, Mohammed A., Alhussaini, Bakr H., Alaifan, Meshari A., Bin-Taleb, Yagoub, Shaik, Noor Ahmad, Al-Aama, Jumana Yousuf, Elango, Ramu, Saadah, Omar I.
Publicado en Biosci Rep (2021)

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 en 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 en 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 en 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 en PLoS One (2017)