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Secured Dynamic Request Scheduling and Optimal CSP Selection for Analyzing Cloud Service Performance Using Intelligent Approaches

IEEE access, 2023, Vol.11, p.140914-140933

2023

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Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

Frontiers in genetics, 2024-08, Vol.15

2024

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Machine Learning Approach to Classification of Online Users by Exploiting Information Seeking Behavior

IEEE access, 2024, Vol.12, p.53234-53249

2024

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UHPLC, ATR-FTIR analysis of Nymphoides indica rhizome extract and determination of antioxidant & antibiofilm potential

Main group chemistry, 2022-01, Vol.21 (1), p.157-166

2022

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Development and Evaluation of Essential Oil-Based Nanoemulgel Formulation for the Treatment of Oral Bacterial Infections

Gels, 2023-03, Vol.9 (3), p.252

2023

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Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans

Journal of Taibah University for Science, 2023-12, Vol.17 (1)

2023

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Lumateperone Interact with S-Protein of Ebola Virus and TIM-1 of Human Cell Membrane: Insights from Computational Studies

Applied sciences, 2022-09, Vol.12 (17), p.8820

2022

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CLINICAL PRESENTATION OF AN EXTENDED CONSANGUINEOUS FAMILY INHERITING WOOLLY HAIR HYPOTRICHOSIS

Gomal journal of medical sciences, 2018-12, Vol.16 (1), p.24

Khan, Muzammil Ahmad

2018

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MICROPHTHALMIA: AN IMPORTANT GENETIC EYE DISORDER

Gomal journal of medical sciences, 2017-01, Vol.14 (3)

Muzammil Ahmad Khan

2017

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Virtual 3D Tour: A User Experience for On-Campus Orientation

Pakistan Journal of Scientific Research, 2023-07, Vol.3 (1), p.32-37

2023

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Identification of IGLI1/I and IKIAA0825/I Variants in Two Families with Postaxial Polydactyly

Genes, 2023-04, Vol.14 (4)

2023

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Expression analysis of tumour necrosis factor alpha (TNF-α) and alkaline phosphatase in occupational workers exposed to low dose of X-radiation: A case-control study

Journal of the Pakistan Medical Association, 2020-11, Vol.70 (11), p.1887-1896

2020

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A novel homozygous splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families

Asian journal of andrology, 2024-09

2024

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The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations: Genetics of ARNSID

Annals of human genetics, 2016-11, Vol.80 (6), p.342-368

2016

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A SYSTEMATIC LITERATURE REVIEW ON SECURITY ISSUES IN CLOUD COMPUTING USING EDGE COMPUTING AND BLOCKCHAIN: THREAT, MITIGATION, AND FUTURE TRENDS

Malaysian journal of computer science, 2023-12, Vol.36 (4), p.347-367

2023

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In silico Analysis of PRODH Mutations and their biological significance in disease etiology

Abasyn Journal Life Sciences, 2022-06 (Volume 5 Issue 1), p.72-83

2022

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Ophthalmo-genetic analysis of Pakistani patients with nonsyndromic oculocutaneous albinism through whole exome sequencing

Journal of the Pakistan Medical Association, 2017-05, Vol.67 (5), p.790-792

2017

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In Silico Analysis of Honeybee Venom Protein Interaction with Wild Type and Mutant (A82V + P375S) Ebola Virus Spike Protein

Biologics (Basel, Switzerland), 2022-01, Vol.2 (1), p.45-55

2022

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Medico-Genetics of Oculocutaneous Albinism; An Updated Study with Pakistani Perspective

Pakistan journal of medical research, 2015-03, Vol.54 (1), p.33A

2015

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MATERNAL CONSANGUINITY: THE MOST PROBABLE CAUSATIVE FACTOR OF GENETIC EYE DISORDERS

Gomal journal of medical sciences, 2017-01, Vol.14 (3)

2017

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Crispr/Cas9 Endonucleases: A New Era of Genetic Engineering

Abasyn Journal Life Sciences, 2021-12 (Volume 4 Issue 2), p.29-39

2021

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Role Of Artificial Intelligence in Big Database Management

The Asian Bulletin of Big Data Management, 2024-05, Vol.4 (2)

2024

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Comparative analysis of autosomal and X-linked genes involved in nonspecific cognitive impairment

Pakistan journal of medical research, 2012-03, Vol.51 (1), p.21

2012

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SKIN PORT: A NOVEL ROUTE FOR DRUG DELIVERY

Gomal journal of medical sciences, 2015-01, Vol.12 (3)

2015

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The Role and Impact of Artificial Intelligence on Project Management

The Asian Bulletin of Big Data Management, 2024-05, Vol.4 (2)

2024

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Secured Dynamic Request Scheduling and Optimal CSP Selection for Analyzing Cloud Service Performance Using Intelligent Approaches

Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

Machine Learning Approach to Classification of Online Users by Exploiting Information Seeking Behavior

UHPLC, ATR-FTIR analysis of Nymphoides indica rhizome extract and determination of antioxidant & antibiofilm potential

Development and Evaluation of Essential Oil-Based Nanoemulgel Formulation for the Treatment of Oral Bacterial Infections

Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans

Lumateperone Interact with S-Protein of Ebola Virus and TIM-1 of Human Cell Membrane: Insights from Computational Studies

CLINICAL PRESENTATION OF AN EXTENDED CONSANGUINEOUS FAMILY INHERITING WOOLLY HAIR HYPOTRICHOSIS

MICROPHTHALMIA: AN IMPORTANT GENETIC EYE DISORDER

Virtual 3D Tour: A User Experience for On-Campus Orientation

Identification of IGLI1/I and IKIAA0825/I Variants in Two Families with Postaxial Polydactyly

Expression analysis of tumour necrosis factor alpha (TNF-α) and alkaline phosphatase in occupational workers exposed to low dose of X-radiation: A case-control study

A novel homozygous splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families

The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations: Genetics of ARNSID

A SYSTEMATIC LITERATURE REVIEW ON SECURITY ISSUES IN CLOUD COMPUTING USING EDGE COMPUTING AND BLOCKCHAIN: THREAT, MITIGATION, AND FUTURE TRENDS

In silico Analysis of PRODH Mutations and their biological significance in disease etiology

Ophthalmo-genetic analysis of Pakistani patients with nonsyndromic oculocutaneous albinism through whole exome sequencing

In Silico Analysis of Honeybee Venom Protein Interaction with Wild Type and Mutant (A82V + P375S) Ebola Virus Spike Protein

Medico-Genetics of Oculocutaneous Albinism; An Updated Study with Pakistani Perspective

MATERNAL CONSANGUINITY: THE MOST PROBABLE CAUSATIVE FACTOR OF GENETIC EYE DISORDERS

Crispr/Cas9 Endonucleases: A New Era of Genetic Engineering

Role Of Artificial Intelligence in Big Database Management

Comparative analysis of autosomal and X-linked genes involved in nonspecific cognitive impairment

SKIN PORT: A NOVEL ROUTE FOR DRUG DELIVERY

The Role and Impact of Artificial Intelligence on Project Management

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