Search Results - "Rauf, Sobiah"
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Unveiling forensically relevant biogeographic, phenotype and Y-chromosome SNP variation in Pakistani ethnic groups using a customized hybridisation enrichment forensic intelligence panel
Published in PloS one (17-02-2022)“…Massively parallel sequencing following hybridisation enrichment provides new opportunities to obtain genetic data for various types of forensic testing and…”
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2
Novel variants underlying autosomal recessive intellectual disability in Pakistani consanguineous families
Published in BMC medical genetics (24-03-2020)“…Intellectual disability (ID) is both a clinically diverse and genetically heterogeneous group of disorder, with an onset of cognitive impairment before the age…”
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3
Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
Published in Human genetics (01-08-2014)“…In this study, we have performed autozygosity mapping on a large consanguineous Pakistani family segregating with intellectual disability. We identified two…”
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4
Identification of bioflavonoid as fusion inhibitor of dengue virus using molecular docking approach
Published in Informatics in medicine unlocked (2016)“…Dengue virus with four distinct serotypes belongs to Flavivirus, poses a significant threat to human health and becomes an emerging global problem. Membrane…”
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5
Identification of novel mutation in the HR gene responsible for atrichia with papular lesions in a Pakistani family
Published in Journal of dermatology (01-11-2013)Get full text
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6
A novel single base pair duplication in WDR62 causes primary microcephaly
Published in BMC medical genetics (11-10-2014)Get full text
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7
Extraction of Fish Collagen Peptides from Fish Waste through Fermentation using Lactobacillus Bacteria
Published in Life and Science (05-10-2023)“…Objective: To introduce a novel technique for extracting fish collagen peptides from fish waste. It could be a cheap and safe technique for obtaining peptides…”
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8
In silico design of multi-epitope vaccines against the hantaviruses by integrated structural vaccinology and molecular modeling approaches
Published in PloS one (23-07-2024)“…Hantaviruses are single-stranded RNA viruses belonging to the family Bunyaviridae that causes hantavirus cardiopulmonary syndrome (HCPS) and hemorrhagic fever…”
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9
Unveiling forensically relevant biogeographic, phenotype and Y-chromosome SNP variation in Pakistani ethnic groups using a customized hybridisation enrichment forensic intelligence panel
Published in PloS one (01-01-2022)“…Massively parallel sequencing following hybridisation enrichment provides new opportunities to obtain genetic data for various types of forensic testing and…”
Get full text
Journal Article -
10
Exploring evolution of brain genes involved in microcephaly through phylogeny and synteny analysis
Published in Theoretical biology and medical modelling (22-10-2013)“…Human brain development is a complicated process. When normal growth and development of brain or central nervous system is impaired, it leads to…”
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11
A novel single base pair duplication in WDR62 causes primary microcephaly
Published in BMC genetics (11-10-2014)“…Primary microcephaly is a disorder of the brain resulting in a reduced head circumference that can come along with intellectual disability but with hardly any…”
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12
In Silico Studies of C3 Metabolic Pathway Proteins of Wheat (Triticum aestivum)
Published in BioMed research international (01-01-2013)“…Photosynthesis is essential for plant productivity and critical for plant growth. More than 90% of plants have a C3 metabolic pathway primarily for carbon…”
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13
In silico studies of C 3 metabolic pathway proteins of wheat (Triticum aestivum)
Published in BioMed research international (2013)“…Photosynthesis is essential for plant productivity and critical for plant growth. More than 90% of plants have a C3 metabolic pathway primarily for carbon…”
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14
In silico studies of [C.sub.3] metabolic pathway proteins of wheat
Published in BioMed research international (01-01-2013)Get full text
Journal Article -
15
Identification of novel mutation in the HR gene responsible for atrichia with papular lesions in a P akistani family
Published in Journal of dermatology (01-11-2013)Get full text
Journal Article