EVALUASI PENGENDALIAN INTERN ATAS SISTEM DAN PROSEDUR TERHADAP PIUTANG USAHA PADA PT. TELEKOMUNIKASI INDONESIA (Persero) Tbk REGIONAL V (JAWA TIMUR, BALI, DAN NUSA TENGGARA)

by AHMAD SIDDIQI A., 041310113054
Published 2016

Stories From the Frontlines: Decolonising Social Contracts for Disasters

by Siddiqi, Ayesha, Canuday, Jose Jowel P
Published 2018

Bovine serum albumin protein-based liquid crystal biosensors for optical detection of toxic heavy metals in water

by Ul Amin, N., Siddiqi, H.M., Lin, Y.K., Hussain, Z., Majeed, N.
Published 2021

Structural and functional insights into a novel homozygous missense pathogenic variant in CUL7 identified in consanguineous Pakistani family

by Zaka, Ayesha, Yousaf, Maha, Shahzad, Shaheen, Rao, Hadi Zahid, Foo, Jia Nee, Siddiqi, Saima
Published 2023

Short- and long-term changes in blood miRNA levels after nanogold injection in rats-potential biomarkers of nanoparticle exposure

by Chew, W.-S., Poh, K.-W., Siddiqi, N.J., Alhomida, A.S., Yu, L.E., Ong, W.-Y.
Published 2014

Cryptanalysis of Two Anonymous Buyer-Seller Watermarking Protocols and an Improvement for True Anonymity

by GOI, Bok-Min, PHAN, Raphael C. W., YANG, Yanjiang, BAO, Feng, DENG, Robert H., Siddiqi, M. U.
Published 2004

Novel phytochemical antibiotic conjugates as multitarget inhibitors of pseudomononas aeruginosa GyrB/ParE and DHFR

by Jayaraman, Premkumar, Lim, ChuSing, Siddiqi, Mohammad Imran, Sakharkar, Kishore R., Dhillon, Sarinder K., Sakharkar, Meena K.
Published 2014

Hybrid-drug design targeting pseudomonas aeruginosa DHPS and DHFR

by Jayaraman, Premkumar, Daniel, Lim Chu Siang, Siddiqi, Mohammad Imran, Dhillon, Sarinder Kaur, Sakharkar, Kishore R., Sakharkar, Meena K.
Published 2014

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

by Ajmal, M, Mir, A, Wahid, S, Khor, C.C, Foo, J.N, Siddiqi, S, Kauser, M, Malik, S.A, Nasir, M
Published 2020

A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani family

by Kausar, Mehran, Chew, Elaine Guo Yan, Ullah, Hazrat, Anees, Mariam, Khor, Chiea Chuen, Foo, Jia Nee, Makitie, Outi, Siddiqi, Saima
Published 2019

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

by Kausar, Mehran, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Makitie, Outi, Asif Mir, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam
Published 2019

Apoptosis induced by JAK2 inhibition is mediated by Bim and enhanced by the BH3 mimetic ABT-737 in JAK2 mutant human erythroid cells

by Will, B., Siddiqi, T., Jorda, M.A., Luptakova, K., Staber, P.B., Costa, D.B., Kobayashi, S., Steidl, U., Tenen, D.G., Shimamura, T.
Published 2011

Adolescent girls? recommendations for the design of a Human Papillomavirus Vaccination Program in Sindh, Pakistan: A qualitative study

by Rozina Feroz Ali, Danya Arif Siddiqi, Amna Mirza, Nowshaba Naz, Sara Abdullah, Gayatri Kembhavi, Clarence Tam, Vittoria Offeddu, Subhash Chandir
Published 2022

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

by Ajmal, Muhammad, Mir, Asif, Wahid, Sughra, Khor, Chiea Chuen, Foo, Jia Nee, Siddiqi, Saima, Kauser, Mehran, Malik, Salman Akbar, Nasir, Muhammad
Published 2018

Variations in regulations to control standards for training and licensing of physicians: a multi-country comparison

by Aftab, Wafa, Khan, Mishal, Rego, Sonia, Chavan, Nishant, Rahman-Shepherd, Afifah, Sharma, Isha, Wu, Shishi, Zeinali, Zahra, Hasan, Rumina, Siddiqi, Sameen
Published 2022

Genetics of vascular dementia - review from the ICVD working group

by Ikram, M.A, Bersano, A, Manso-Calderón, R, Jia, J.-P, Schmidt, H, Middleton, L, Nacmias, B, Siddiqi, S, Adams, H.H.H
Published 2020

Case report: expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease

by Ravindran, Ethiraj, Ullah, Noor, Mani, Shyamala, Chew, Elaine Guo Yan, Tandiono, Moses, Foo, Jia Nee, Khor, Chiea Chuen, Kaindl, Angela M., Siddiqi, Saima
Published 2023

A novel splice-site mutation in ALS establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias

by Siddiqi S., Foo J.N., Vu A., Azim S., Silver D.L., Mansoor A., Tay S.K.H., Abbasi S., Hashmi A.H., Janjua J., Khalid S., Tai E.S., Yeo G.W., Khor C.C.
Published 2018

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy

by Seco, C.Z, Castells-Noba A., Joo, S.-H, Schraders, M., Foo, J.N., Van Der Voet, M., Velan, S.S, Nijhof, B., Oostrik, J., De Vrieze, E., Katana, R., Mansoor, A., Huynen, M., Szklarczyk, R., Oti, M., Tranebjarg, L., Van Wijk, E., Scheffer-De Gooyert, J.M., Siddique, S., Baets, J., De Jonghe, P., Kazmi, S.A.R., Sadananthan, S.A, Van De Warrenburg, B.P., Khor, C.C, Göpfert, M.C., Qamar, R., Schenck, A., Kremer, H., Siddiqi, S.
Published 2020

Medial representations : mathematics, algorithms and applications

Published 2017