A comparison of four fibrosis indexes in chronic HCV: development of new fibrosis-cirrhosis index (FCI) von Ahmad, Waqar, Ijaz, Bushra, Javed, Fouzia T, Gull, Sana, Kausar, Humaira, Sarwar, Muhammad T, Asad, Sultan, Shahid, Imran, Sumrin, Aleena, Khaliq, Saba, Jahan, Shah, Pervaiz, Asim, Hassan, Sajida

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Claudin-1 required for HCV virus entry has high potential for phosphorylation and O-glycosylation von Ahmad, Waqar, Shabbiri, Khadija, Ijaz, Bushra, Asad, Sultan, Sarwar, Muhammad T, Gull, Sana, Kausar, Humera, Fouzia, Kiran, Shahid, Imran, Hassan, Sajida

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A brief review on molecular, genetic and imaging techniques for HCV fibrosis evaluation von Ahmad, Waqar, Ijaz, Bushra, Gull, Sana, Asad, Sultan, Khaliq, Saba, Jahan, Shah, Sarwar, Muhammad T, Kausar, Humera, Sumrin, Aleena, Shahid, Imran, Hassan, Sajida

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Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency von Ansar, Muhammad, Ranza, Emmanuelle, Shetty, Madhur, Paracha, Sohail A, Azam, Maleeha, Kern, Ilse, Iwaszkiewicz, Justyna, Farooq, Omer, Pournaras, Constantin J, Malcles, Ariane, Kecik, Mateusz, Rivolta, Carlo, Muzaffar, Waqar, Qurban, Aziz, Ali, Liaqat, Aggoun, Yacine, Santoni, Federico A, Makrythanasis, Periklis, Ahmed, Jawad, Qamar, Raheel, Sarwar, Muhammad T, Henry, L Keith, Antonarakis, Stylianos E

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Association of laboratory parameters with viral factors in patients with hepatitis C von Ijaz, Bushra, Ahmad, Waqar, Javed, Fouzia T, Gull, Sana, Sarwar, Muhammad T, Kausar, Humera, Asad, Sultan, Jahan, Shah, Khaliq, Saba, Shahid, Imran, Sumrin, Aleena, Hassan, Sajida

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De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects von Manole, Andreea, Efthymiou, Stephanie, O’Connor, Emer, Mendes, Marisa I., Jennings, Matthew, Maroofian, Reza, Davagnanam, Indran, Mankad, Kshitij, Lopez, Maria Rodriguez, Salpietro, Vincenzo, Harripaul, Ricardo, Badalato, Lauren, Walia, Jagdeep, Francklyn, Christopher S., Athanasiou-Fragkouli, Alkyoni, Sullivan, Roisin, Desai, Sonal, Baranano, Kristin, Zafar, Faisal, Rana, Nuzhat, Ilyas, Muhammed, Horga, Alejandro, Kara, Majdi, Mattioli, Francesca, Goldenberg, Alice, Griffin, Helen, Piton, Amelie, Henderson, Lindsay B., Kara, Benyekhlef, Aslanger, Ayca Dilruba, Raaphorst, Joost, Pfundt, Rolph, Portier, Ruben, Shinawi, Marwan, Kirby, Amelia, Christensen, Katherine M., Wang, Lu, Rosti, Rasim O., Paracha, Sohail A., Sarwar, Muhammad T., Jenkins, Dagan, Ahmed, Jawad, Santoni, Federico A., Ranza, Emmanuelle, Iwaszkiewicz, Justyna, Cytrynbaum, Cheryl, Weksberg, Rosanna, Wentzensen, Ingrid M., Guillen Sacoto, Maria J., Si, Yue, Telegrafi, Aida, Andrews, Marisa V., Baldridge, Dustin, Gabriel, Heinz, Mohr, Julia, Oehl-Jaschkowitz, Barbara, Debard, Sylvain, Senger, Bruno, Fischer, Frédéric, van Ravenwaaij, Conny, Fock, Annemarie J.M., Stevens, Servi J.C., Bähler, Jürg, Nasar, Amina, Mantovani, John F., Manzur, Adnan, Sarkozy, Anna, Smith, Desirée E.C., Salomons, Gajja S., Ahmed, Zubair M., Riazuddin, Shaikh, Riazuddin, Saima, Usmani, Muhammad A., Seibt, Annette, Ansar, Muhammad, Antonarakis, Stylianos E., Vincent, John B., Ayub, Muhammad, Grimmel, Mona, Jelsig, Anne Marie, Hjortshøj, Tina Duelund, Karstensen, Helena Gásdal, Hummel, Marybeth, Haack, Tobias B., Jamshidi, Yalda, Distelmaier, Felix, Horvath, Rita, Gleeson, Joseph G., Becker, Hubert, Mandel, Jean-Louis, Koolen, David A., Houlden, Henry

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Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts von Ansar, Muhammad, Chung, Hyung-lok, Taylor, Rachel L., Nazir, Aamir, Imtiaz, Samina, Sarwar, Muhammad T., Manousopoulou, Alkistis, Makrythanasis, Periklis, Saeed, Sondas, Falconnet, Emilie, Guipponi, Michel, Pournaras, Constantin J., Ansari, Maqsood A., Ranza, Emmanuelle, Santoni, Federico A., Ahmed, Jawad, Shah, Inayat, Gul, Khitab, Black, Graeme CM, Bellen, Hugo J., Antonarakis, Stylianos E.

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Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature von Ansar, Muhammad, Paracha, Sohail Aziz, Serretti, Alessandro, Sarwar, Muhammad T, Khan, Jamshed, Ranza, Emmanuelle, Falconnet, Emilie, Iwaszkiewicz, Justyna, Shah, Sayyed Fahim, Qaisar, Azhar Ali, Santoni, Federico A, Zoete, Vincent, Megarbane, Andre, Ahmed, Jawad, Colombo, Roberto, Makrythanasis, Periklis, Antonarakis, Stylianos E

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Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature von Ansar, Muhammad, Chung, Hyung-lok, Al-Otaibi, Ali, Elagabani, Mohammad Nael, Ravenscroft, Thomas A., Paracha, Sohail A., Scholz, Ralf, Abdel Magid, Tayseer, Sarwar, Muhammad T., Shah, Sayyed Fahim, Qaisar, Azhar Ali, Makrythanasis, Periklis, Marcogliese, Paul C., Kamsteeg, Erik-Jan, Falconnet, Emilie, Ranza, Emmanuelle, Santoni, Federico A., Aldhalaan, Hesham, Al-Asmari, Ali, Faqeih, Eissa Ali, Ahmed, Jawad, Kornau, Hans-Christian, Bellen, Hugo J., Antonarakis, Stylianos E.

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Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features von Ansar, Muhammad, Ullah, Farid, Paracha, Sohail A., Adams, Darius J., Lai, Abbe, Pais, Lynn, Iwaszkiewicz, Justyna, Millan, Francisca, Sarwar, Muhammad T., Agha, Zehra, Shah, Sayyed Fahim, Qaisar, Azhar Ali, Falconnet, Emilie, Zoete, Vincent, Ranza, Emmanuelle, Makrythanasis, Periklis, Santoni, Federico A., Ahmed, Jawad, Katsanis, Nicholas, Walsh, Christopher, Davis, Erica E., Antonarakis, Stylianos E.

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HCV genotype-specific correlation with serum markers: higher predictability for genotype 4a von Ahmad, Waqar, Ijaz, Bushra, Javed, Fouzia T, Kausar, Humera, Sarwar, Muhammad T, Gull, Sana, Asad, Sultan, Shahid, Imran, Hassan, Sajida

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NS4A protein as a marker of HCV history suggests that different HCV genotypes originally evolved from genotype 1b von Sarwar, Muhammad T, Kausar, Humera, Ijaz, Bushra, Ahmad, Waqar, Ansar, Muhammad, Sumrin, Aleena, Ashfaq, Usman A, Asad, Sultan, Gull, Sana, Shahid, Imran, Hassan, Sajida

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Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature... von Ansar, Muhammad, Ebstein, Frédéric, Özkoç, Hayriye, Paracha, Sohail A, Iwaszkiewicz, Justyna, Gesemann, Matthias, Zoete, Vincent, Ranza, Emmanuelle, Santoni, Federico A, Sarwar, Muhammad T, Ahmed, Jawad, Krüger, Elke, Bachmann-Gagescu, Ruxandra, Antonarakis, Stylianos E

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Serine 204 phosphorylation and O-β-GlcNAC interplay of IGFBP-6 as therapeutic indicator to regulate IGF-II functions in viral mediated hepatocellular carcinoma von Ahmad, Waqar, Shabbiri, Khadija, Ijaz, Bushra, Asad, Sultan, Nazar, Noreen, Nazar, Shazia, Fouzia, Kiran, Kausar, Humera, Gull, Sana, Sarwar, Muhammad T, Shahid, Imaran, Hassan, Sajida

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Life Cycle and Development of Diptera von Muhammad Sarwar

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Serine 204 phosphorylation and O- [beta] -GlcNAC interplay of IGFBP-6 as therapeutic indicator to regulate IGF-II functions in viral mediated hepatocellular carcinoma von Ahmad, Waqar, Shabbiri, Khadija, Ijaz, Bushra, Asad, Sultan, Nazar, Noreen, Nazar, Shazia, Fouzia, Kiran, Kausar, Humera, Gull, Sana, Sarwar, Muhammad T, Shahid, Imaran, Hassan, Sajida

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Biallelic variants in PSMB1 encoding the proteasome subunit beta 6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short sta... von Ansar, Muhammad, Ebstein, Frederic, Oezkoc, Hayriye, Paracha, Sohail A., Iwaszkiewicz, Justyna, Gesemann, Matthias, Zoete, Vincent, Ranza, Emmanuelle, Santoni, Federico A., Sarwar, Muhammad T., Ahmed, Jawad, Krueger, Elke, Bachmann-Gagescu, Ruxandra, Antonarakis, Stylianos E.

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Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature... von Ansar, Muhammad, Ebstein, Frédéric, Özkoç, Hayriye, Paracha, Sohail A, Iwaszkiewicz, Justyna, Gesemann, Matthias, Zoete, Vincent, Ranza, Emmanuelle, Santoni, Federico A, Sarwar, Muhammad T, Ahmed, Jawad, Krüger, Elke, Bachmann-Gagescu, Ruxandra, Antonarakis, Stylianos E

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Identification, Characterization, and Treatment for a Taurine Transporter (SLC6A6) Variant Resulting in Taurine Deficiency and Pathologies in a Consanguineous Family von Henry, L. Keith, Ansar, Muhammad, Ranza, Emmanuella, Shetty, Madhur, Paracha, Sohail A., Azam, Maleeha, Kern, Ilse, Iwaszkiewicz, Justyna, Farooq, Omer, Pournaras, Constantin J., Malcles, Ariane, Kecik, Mateusz, Muzaffar, Waqar, Qurban, Aziz, Ali, Liaqat, Aggoun, Yacine, Santoni, Federico A., Makrythanasis, Periklis, Ahmed, Jawad, Qamar, Raheel, Rivolta, Carlo, Sarwar, Muhammad T., Antonarakis, Stylianos E.

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Tropical Plant Species and Technological Interventions for Improvement

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