Combining ability assessment in Helianthus annuus L. through line tester analysis for quantitative traits and quality parameters von Muhammad, Azeem ur Rahman Khalid, Dr, Muhammad Ahsan Iqbal, Muhammad, Zubair, Amanullah, Zafar, Asad, Butt, Sulman, Abid, Yasir, Shahzad, Muhammad, Ajmal, Ali, Adnan Liaqat

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Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous families von Umair, Muhammad, Hassan, Annum, Jan, Abid, Ahmad, Farooq, Imran, Muhammad, Samman, Muhammad I, Basit, Sulman, Ahmad, Wasim

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Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia von Ullah, Asmat, Shah, Abid Ali, Syed, Fibhaa, Mahmood, Arif, Ur Rehman, Hassan, Khurshid, Beenish, Samad, Abdus, Ahmad, Wasim, Basit, Sulman

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Potential enzyme inhibitor triazoles from aliphatic esters: Synthesis, enzyme inhibition and docking studies von Sultana, Rifhat, Abid, Obaid-ur-Rahman, Sultana, Nighat, Fakhar-e-Alam, M., Siddique, Muhammad Hussnain, Atif, M., Nawaz, Mohsin, Wadood, Abdul, Rehman, Ashfaq Ur, Farooq, W.A., Shafeeq, Sulman, Afzal, Muhammad

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Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia von Akbar, Warda, Ullah, Asmat, Haider, Nighat, Suleman, Sufyan, Khan, Fati Ullah, Shah, Abid Ali, Sikandar, Muhammad Atif, Basit, Sulman, Ahmad, Wasim

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Design, synthesis, in vitro and in silico studies of naproxen derivatives as dual lipoxygenase and α-glucosidase inhibitors von Sardar, Asma, Abid, Obaid-ur-Rahman, Daud, Saima, Fakhar-e-Alam, M., Siddique, Muhammad Hussnain, Ashraf, Muhammad, Shahid, Wardah, Ejaz, Syeda Abida, Atif, M., Ahmad, Shafiq, Shafeeq, Sulman, Afzal, Muhammad

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Discovery of Mutated MUC3A Gene As a Novel Transcription Factor Exclusively Associated with Accelerated Phase Chronic Myeloid Leukemia: Hunt for Common Biomarker of Fatal CML Progr... von Shahid, Sameen, Sabar, Muhammad, Jamil, Abid, Khokar, Muhammad Abbas, Absar, Muhammad, Iqbal, Mudassar, Shammas, Masood A., Saglio, Giuseppe, Basit, Sulman, Afzal, Sibtain, Ramzan, Khushnooda, Aleem, Aamer, Mahmood, Amer, Alanzazi, Nawaf, Asif, Muhammad Javed, Rasool, Mahmood, Khalid, Ahmad, Iqbal, Zafar

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Integrated Genomic Analysis Identifies ANKRD36 Gene as a Novel and Common Biomarker of Disease Progression in Chronic Myeloid Leukemia von Iqbal, Zafar, Absar, Muhammad, Akhtar, Tanveer, Aleem, Aamer, Jameel, Abid, Basit, Sulman, Ullah, Anhar, Afzal, Sibtain, Ramzan, Khushnooda, Rasool, Mahmood, Karim, Sajjad, Mirza, Zeenat, Iqbal, Mudassar, AlMajed, Maryam, AlShehab, Buthinah, AlMukhaylid, Sarah, AlMutairi, Nouf, Al-anazi, Nawaf, Sabar, Muhammad Farooq, Arshad, Muhammad, Asif, Muhammad, Shammas, Masood, Mahmood, Amer

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Molecular Dynamic Simulation Analysis of a Novel Missense Variant in ICYB5R3/I Gene in Patients with Methemoglobinemia von Ullah, Asmat, Shah, Abid Ali, Syed, Fibhaa, Mahmood, Arif, Ur Rehman, Hassan, Khurshid, Beenish, Samad, Abdus, Ahmad, Wasim, Basit, Sulman

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Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expans... von Ullah, Asmat, Shah, Abid Ali, Alluqmani, Majed, Haider, Nighat, Aman, Hasan, Alfadhli, Fatima, Almatrafi, Ahmad M., Albalawi, Alia M., Krishin, Jai, Ullah Khan, Fati, Anjam, Bilal Ali, Abdullah, Lozano, Elionora Peña, Samad, Abdus, Ahmad, Wasim, Hansen, Torben, Xia, Kun, Basit, Sulman

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Prognostic Stratification of Acute Myeloid Leukemia and Mylodysplastic Syndrome Patients on the Basis of Genetic Variations von ALI, Muhammad, Basit, Sulman, Masood, Muhammad tariq, Yousafzai, Yasar Mehmood, Naseer, Asif, Rahman, Sadeeq ur, Jelani, Musharraf, Khan, Imran, Khan, Yousaf, Jameel, Abid, Ahmed, Jawad, Taj, Abid Sohail

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Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2 von Jan, Abid, Basit, Sulman, Wakil, Salma M, Ramzan, Khushnooda, Ahmad, Wasim

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Investigations on Novel Gene Variants Associated with Longterm Response to Tyrosine Kinase Inhibitors (TKIs) in Chronic Myeloid Leukemia: Implication in TKI-Cessation Clinical Trai... von Iqbal, Zafar, Absar, Muhammad, Jameel, Abid, Akhtar, Tanveer, Basit, Sulman, Mahmood, Aamer, Aleem, Aamir, Alanazi, Nawaf, Anhar, Ullah, Khalid, Naila Batool, Afzal, Sibtain, Hashmi, Jamil Amjad, Akram, Afia M, Ramzan, Khushnooda, Rasool, Mahmood, Aziz, Muhammad Hasaan, Sabar, Muhammad Farooq, Iqbal, Mudassar, Khalid, Ahmad Mukhtar

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Whole exome sequencing identifies a novel FANCD2 gene splice site mutation associated with disease progression in chronic myeloid leukemia: Implication in targeted therapy of advan... von Absar, Muhammad, Mahmood, Amer, Akhtar, Tanveer, Basit, Sulman, Ramzan, Khushnooda, Jameel, Abid, Afzal, Sibtain, Ullah, Anhar, Qureshi, Kulsoom, Alanazi, Nawaf, Iqbal, Zafar

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A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia von Jan, Abid, Basit, Sulman, Wakil, Salma M., Ramzan, Khushnooda, Ahmad, Wasim

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