Search Results - "AZHAR, Aysha"
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CORONAVIRUS DISEASE 2019 (COVID-19)
Published in Journal of University Medical & Dental College (25-09-2020)“…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
Published in PloS one (01-04-2014)“…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
Published in Pakistan journal of medical sciences (31-10-2017)“…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
Published in Journal of medical microbiology (01-09-2017)“…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
Published in The professional medical journal (10-02-2020)“…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
Published in Curēus (Palo Alto, CA) (29-06-2020)“…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
Published in Pakistan journal of medical sciences (28-02-2021)“…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
Published in Scientific reports (12-10-2012)“…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
Published in European journal of human genetics : EJHG (01-06-2010)“…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
Published in EJD. European journal of dermatology (01-07-2012)“…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
Published in EJD. European journal of dermatology (01-07-2010)“…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
Published in Journal of pediatric hematology/oncology (01-03-2012)“…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
Published in PloS one (01-04-2014)“…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
Published in Pakistan journal of medical sciences (30-09-2011)“…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
Published in Pakistan journal of medical sciences (30-06-2011)Get full text
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