Search Results - "Azhar, Aysha"

CORONAVIRUS DISEASE 2019 (COVID-19) by Aysha Azhar

“…The epidemic of 2019 novel coronavirus (2019-nCoV) has been emerged from a major city named Wuhan in the Hubei Province of China. It appears to have the…”
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Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis by Raykova, Doroteya, Klar, Joakim, Azhar, Aysha, Khan, Tahir Naeem, Malik, Naveed Altaf, Iqbal, Muhammad, Tariq, Muhammad, Baig, Shahid Mahmood, Dahl, Niklas

“…Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heritable disorders characterized by brittle hair, hypotrichosis,…”
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Rapid screening of pyogenic Staphylococcus aureus for confirmation of genus and species, methicillin resistance and virulence factors by using two novel multiplex PCR by Haque, Abdul, Haque, Asma, Saeed, Muhammad, Azhar, Aysha, Rasool, Samreen, Shan, Sidra, Ehsan, Beenish, Nisar, Zohaib

“…Emergence of methicillin resistant (MRSA) is a major medical problem of current era. These bacteria are resistant to most drugs and rapid diagnosis can provide…”
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Detection of high levels of resistance to linezolid and vancomycin in Staphylococcus aureus by Azhar, Aysha, Rasool, Samreen, Haque, Asma, Shan, Sidra, Saeed, Muhammad, Ehsan, Beenish, Haque, Abdul

“…Both methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-sensitive S. aureus (MSSA) are rapidly overcoming the current array of drugs. One…”
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MMP-2 levels evaluation and their relationship with breast cancer progression by Yaqoob, Ifrah, Saeed, Muhammad, Azhar, Aysha

“…Matrix metalloproteinases (MMPs) play significant part in the tumor development, metastasis and invasion by proteolytic degradation of basement membrane and…”
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Venetoclax in the Treatment of Chronic Lymphocytic Leukemia: Evidence, Expectations, and Future Prospects by Tariq, Saba, Tariq, Sundus, Khan, Maliha, Azhar, Aysha, Baig, Mukhtiar

“…Chronic lymphocytic leukemia (CLL) is the most common form of leukemia in the western adult population; it is also prevalent worldwide. The B cell lymphoma-2…”
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High frequency of simultaneous presence of ESBL and carbapenemase producers among nosocomial coliform isolates in Faisalabad, Pakistan by Irfan, Sofia, Azhar, Aysha, Bashir, Asad, Ahmed, Salman, Haque, Abdul

“…The objective of the current study was to find prevalence of relevant ESBL and carbapenemase producing genes in nosocomial and isolates and to check phenotypic…”
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A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair by Tariq, Muhammad, Azhar, Aysha, Baig, Shahid Mahmood, Dahl, Niklas, Klar, Joakim

“…Mutations in the lipase member H (LIPH) gene cause autosomal recessive hypotrichosis with woolly hair. We report herein on five consanguineous families from…”
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Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS by FAROOQ, Muhammad, TROELSEN, Jesper T, TOMMERUP, Niels, SHAHID MAHMOOD BAIG, KJAER, Klaus W, BOYD, Mette, EIBERG, Hans, HANSEN, Lars, MUHAMMAD SAJID HUSSAIN, SHOAIB UR REHMAN, AZHAR, Aysha, ALI, Amjad, SYEDA MARRIAM BAKHTIAR

“…A cis-regulatory sequence also known as zone of polarizing activity (ZPA) regulatory sequence (ZRS) located in intron 5 of LMBR1 is essential for expression of…”
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A novel mutation in Lysophosphatidic Acid Receptor 6 gene in autosomal recessive hypotrichosis and evidence for a founder effect by AZHAR, Aysha, TARIQ, Muhammad, MAHMOOD BAIG, Shahid, DAHL, Niklas, KLAR, Joakim

“…Mutations in the lysophosphatidic acid receptor 6 (LPAR6) gene cause localized autosomal recessive hypotrichosis. We report six consanguineous families from…”
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Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation by RASOOL, Mahmood, NAWAZ, Sadia, AZHAR, Aysha, WAJID, Muhammad, WESTERMARK, Per, BAIG, Shahid M, KLAR, Joakim, DAHL, Niklas

“…Hair-nail ectodermal dysplasia (HNED; OMIM 602032) constitutes a rare subgroup of ectodermal dysplasias characterised by onychodystrophy, hypotrichosis and…”
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β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan by Mahmood Baig, Shahid, Sabih, Dure, Rahim, Muhammad Kashif, Azhar, Aysha, Tariq, Muhammad, Sajid Hussain, Muhammad, Saqlan Naqvi, Syed Muhammad, Raja, Ghazala Kaukab, Khan, Tahir Naeem, Jameel, Muhammad, Iram, Zahra, Noor, Samia, Baig, Usman Raza, Qureshi, Javed Anver, Baig, Shehla Anjum, Bakhtiar, Syeda Marriam

“…Prenatal diagnosis (PND) of β-thalassemia has been underutilized in Pakistan because of a number of social and economic factors. National Institute for…”
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Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis: e93607 by Raykova, Doroteya, Klar, Joakim, Azhar, Aysha, Khan, Tahir Naeem, Malik, Naveed Altaf, Iqbal, Muhammad, Tariq, Muhammad, Baig, Shahid Mahmood, Dahl, Niklas

“…Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heritable disorders characterized by brittle hair, hypotrichosis,…”
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Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family by Nawaz, Sadia, Tariq, Muhammad, Azhar, Aysha, Rasool, Mahmood, Bakhtiar, Syeda Marriam, Ahmad, Ilyas, ur Rehman, Shoaib, jameel, Muhammad, Khan, Tahir Naeem, Baig, Shehla Anjum, Klar, Joakim, Dahl, Niklas, Baig, Shahid Mahmood

“…Objective: To characterize the disease causing mutation in a large consanguineous Pakistani family with severe Mat de Meleda (MDM) or keratosis palmoplantaris…”
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Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family by Nawaz, Sadia, Tariq, Muhammad, Azhar, Aysha, Rasool, Mahmood, Bakhtiar, Syeda Marriam, Ahmad, Ilyas, ur Rehman, Shoaib, Jameel, Muhammad, Khan, Tahir Naeem, Baig, Shehla Anjum, Klar, Joakim, Dahl, Niklas, Baig, Shahid Mamood

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