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

بواسطة AHMAD SIDDIQI A., 041310113054
منشور في 2016

Stories From the Frontlines: Decolonising Social Contracts for Disasters

بواسطة Siddiqi, Ayesha, Canuday, Jose Jowel P
منشور في 2018

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

بواسطة Ul Amin, N., Siddiqi, H.M., Lin, Y.K., Hussain, Z., Majeed, N.
منشور في 2021

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

بواسطة Zaka, Ayesha, Yousaf, Maha, Shahzad, Shaheen, Rao, Hadi Zahid, Foo, Jia Nee, Siddiqi, Saima
منشور في 2023

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

بواسطة Chew, W.-S., Poh, K.-W., Siddiqi, N.J., Alhomida, A.S., Yu, L.E., Ong, W.-Y.
منشور في 2014

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

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

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

بواسطة Jayaraman, Premkumar, Lim, ChuSing, Siddiqi, Mohammad Imran, Sakharkar, Kishore R., Dhillon, Sarinder K., Sakharkar, Meena K.
منشور في 2014

Hybrid-drug design targeting pseudomonas aeruginosa DHPS and DHFR

بواسطة Jayaraman, Premkumar, Daniel, Lim Chu Siang, Siddiqi, Mohammad Imran, Dhillon, Sarinder Kaur, Sakharkar, Kishore R., Sakharkar, Meena K.
منشور في 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

بواسطة Ajmal, M, Mir, A, Wahid, S, Khor, C.C, Foo, J.N, Siddiqi, S, Kauser, M, Malik, S.A, Nasir, M
منشور في 2020

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

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

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

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

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

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

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

بواسطة Rozina Feroz Ali, Danya Arif Siddiqi, Amna Mirza, Nowshaba Naz, Sara Abdullah, Gayatri Kembhavi, Clarence Tam, Vittoria Offeddu, Subhash Chandir
منشور في 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

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

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

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

Genetics of vascular dementia - review from the ICVD working group

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

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

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

بواسطة 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.
منشور في 2018

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

بواسطة 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.
منشور في 2020

Medial representations : mathematics, algorithms and applications

منشور في 2017