A novel homozygous splice site variant in CERS3 causes autosomal recessive congenital ichthyosis von Jan, Hamadia, Wasif, Naveed, Naqvi, Syed Kamran‐ul‐Hassan, Ullah, Imran, Ahmad, Wasim

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A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31–p36.13 von Ansar, Muhammad, Lee, Kwanghyuk, Naqvi, Syed Kamran-ul-Hassan, Andrade, Paula B, Basit, Sulman, Santos-Cortez, Regie Lyn P, Ahmad, Wasim, Leal, Suzanne M

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Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families von Wasif, Naveed, Naqvi, Syed Kamran ul-Hassan, Basit, Sulman, Ali, Nadir, Ansar, Muhammad, Ahmad, Wasim

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Prevalence of different tick species on livestock and associated equines and canine from different agro-ecological zones of Pakistan von Hussain, Nazeer, Shabbir, Rana Muhammad Kamran, Ahmed, Haroon, Afzal, Muhammad Sohail, Ullah, Shafi, Ali, Abid, Irum, Shumaila, Naqvi, Syed Kamran-Ul-Hassan, Yin, Jianhai, Cao, Jianping

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Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genes von Umm-e-Kalsoom, Basit, Sulman, Kamran-ul-Hassan Naqvi, Syed, Ansar, Muhammad, Ahmad, Wasim

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Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families von AZEEM, Zahid, WASIF, Naveed, BASIT, Sulman, RAZAK, Suhail, WAHEED, Raja Amjad, ISLAM, Adeel, AYUB, Muhammad, KAFAITULLAH,  , KAMRAN-UL-HASSAN NAQVI, Syed, ALI, Ghazanfar, AHMAD, Wasim

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Natural Agents-Mediated Targeting of Histone Deacetylases von Farooqi, Ammad Ahmad, Naqvi, Syed Kamran-ul-Hassan, Perk, Aliye Aras, Yanar, Onur, Tabassum, Sobia, Ahmad, Muhammad Sheeraz, Mansoor, Qaisar, Ashry, Mohamed S., Ismail, Muhammad, Naoum, George E., Arafat, Waleed O.

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TRAIL Mediated Signaling in Pancreatic Cancer von Nogueira, Daniele Rubert, Yaylim, Ilhan, Aamir, Qurratulain, Kahraman, OzlemTimirci, Fayyaz, Sundas, Naqvi, Syed Kamran-Ul-Hassan, Farooqi, Ammad Ahmad

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Genetic analysis of Xp22.3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosis von Ali, Raja Hussain, Mahmood, Sabba, Raza, Syed Irfan, Aziz, Abdul, Irfanullah, Naqvi, Syed Kamran-ul-Hassan, Wasif, Naveed, Ansar, Muhammad, Ahmad, Wasim, Shah, Sayed Hajan, Khan, Bakht Tarin, Zaman, Qaiser, Gul, Ajab, Wali, Abdul, Ali, Ghazanfar, Khan, Saadulah, Khisroon, Muhammad, Basit, Sulman

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A Novel Deletion Mutation in Proteoglycan-4 Underlies Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome in a Consanguineous Pakistani Family von Basit, Sulman, Iqbal, Zafar, Umicevic-Mirkov, Masha, Kamran Ul-Hassan Naqvi, Syed, Coenen, Marieke, Ansar, Muhammad, van Bokhoven, Hans, Ahmad, Wasim

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Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23-22.3 von Naz, Gul, Ali, Ghazanfar, Kamran-ul-Hassan Naqvi, Syed, Azeem, Zahid, Ahmad, Wasim

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Epidemiological and pathological characteristics of Cutaneous Leishmaniasis from Baluchistan Province of Pakistan von Khan, Aisha, Sajid, Rawan, Gul, Shaista, Hussain, Ashiq, Zehri, Mohammad Tahir, Naz, Shumaila, Simsek, Sami, Waseem, Shahid, Afzal, Muhammad Sohail, Naqvi, Syed Kamran Ul Hassan, Qasim, Muhammad, Ahmed, Haroon

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Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia von Azeem, Zahid, Naqvi, Syed Kamran-Ul-Hassan, Ansar, Muhammad, Wali, Abdul, Naveed, Abdul Khaliq, Ali, Ghazanfar, Hassan, Muhammad Jawad, Tariq, Muhammad, Basit, Sulman, Ahmad, Wasim

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miR-421, miR-155 and miR-650: Emerging Trends of Regulation of Cancer and Apoptosis von Farooqi, Ammad Ahmad, Qureshi, Muhammad Zahid, Coskunpinar, Ender, Naqvi, Syed Kamran-Ul-Hassan, Yaylim, Ilhan, Ismail, Muhammad

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Knowledge, Attitudes and Practices Regarding Taeniasis in Pakistan von Bibi, Saba, Kamran, Muhammad, Ahmad, Haroon, Bibi, Kainat, Naqvi, Syed Kamran Ul Hassan, Zuo, Qingqiu, Shah, Naseer Ali, Cao, Jianping

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novel splice-acceptor site mutation in CDH3 gene in a consanguineous family exhibiting hypotrichosis with juvenile macular dystrophy von Kamran-ul-Hassan Naqvi, Syed, Azeem, Zahid, Ali, Ghazanfar, Ahmad, Wasim

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Anticancer Activity of Essential Oils: Targeting of Protein Networks in Cancer Cells von Aras, Aliye, Iqbal, Muhammed Javed, Naqvi, Syed Kamran-Ul-Hassan, Gercek, Yusuf Can, Boztas, Kadir, Gasparri, Maria Luisa, Shatynska-Mytsyk, Iryna, Fayyaz, Sundas, Farooqi, Ammad Ahmad

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Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3) von Azeem, Zahid, Jelani, Musharraf, Naz, Gul, Tariq, Muhammad, Wasif, Naveed, Kamran-ul-Hassan Naqvi, Syed, Ayub, Muhammad, Yasinzai, Masoom, Amin-ud-din, Muhammad, Wali, Abdul, Ali, Ghazanfar, Chishti, Muhammad Salman, Ahmad, Wasim

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A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family von Basit, Sulman, Naqvi, Syed Kamran-ul-Hassan, Wasif, Naveed, Ali, Ghazanfar, Ansar, Muhammad, Ahmad, Wasim

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miR-421, miR-155 and miR-650: Emerging Trends of Regulation of Cancer and Apoptosis von Farooqi, Ammad Ahmad, Qureshi, Muhammad Zahid, Coskunpinar, Ender, Naqvi, Syed Kamran-Ul-Hassan, Yaylim, Ilhan, Ismail, Muhammad

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