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Plant beneficial endophytic bacteria: Mechanisms, diversity, host range and genetic determinants

Microbiological research, 2019-04, Vol.221, p.36-49

2019

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Characterization and applications of glutaminase free L-asparaginase from indigenous Bacillus halotolerans ASN9

PloS one, 2023-11, Vol.18 (11), p.e0288620-e0288620

2023

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Antioxidants and Calcium Modulators Preclude in Vitro Hepatitis B Virus–Induced Mitochondrial Damage

The Turkish Journal of Gastroenterology, 2023-10, Vol.34 (10), p.1052-1061

2023

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A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis‐2 with impaired intellectual development

American journal of medical genetics. Part A, 2021-02, Vol.185 (2), p.355-361

2021

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Restoration of IL-11 and IL-15 cytokine production post calcium modulators and ROS treatment can assist viral clearance both in vitro and in vivo

Iranian journal of basic medical sciences, 2023-02, Vol.26 (2), p.176-182

2023

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Effect of oxidative stress and calcium deregulation on FAM26F (CALHM6) expression during hepatitis B virus infection

BMC infectious diseases, 2021-02, Vol.21 (1), p.228-13, Article 228

2021

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CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis

Breast cancer (Tokyo, Japan), 2019-01, Vol.26 (1), p.11-28

2019

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny

Journal of human genetics, 2018-01, Vol.63 (1), p.97-100

2018

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L237P Substitution in the UROS Gene Causes X-linked Recessive Congenital Erythropoietic Porphyria in Pakistani Consanguineous Family Through Altered Uroporphyrinogen III Binding

Pakistan journal of zoology, 2022-08, Vol.54 (4), p.1849

2022

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Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities

Archives of Dermatological Research, 2017-12, Vol.309 (10), p.773-785

2017

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Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families

BMC medical genetics, 2019-12, Vol.20 (1), p.199-199, Article 199

2019

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Facile Synthesis as well as Structural, Raman, Dielectric and Antibacterial Characteristics of Cu Doped ZnO Nanoparticles

Journal of materials science & technology, 2015-03, Vol.31 (3), p.300-304

2015

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In silico Analysis of Candidate Genes Involved in Sanfilippo Syndrome

Bioautomation, 2015, Vol.19 (1), p.5-14

2015

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Structural and functional insights into a novel homozygous missense pathogenic variant in CUL7 identified in consanguineous Pakistani family

Journal of biomolecular structure & dynamics, 2024-07, Vol.42 (10), p.5092-5103

2024

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Demonstrating the application of Raman spectroscopy together with chemometric technique for screening of asthma disease

Biomedical optics express, 2019-02, Vol.10 (2), p.600-609

2019

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Cost effective and efficient screening of tuberculosis disease with Raman spectroscopy and machine learning algorithms

Photodiagnosis and photodynamic therapy, 2020-12, Vol.32, p.101963-101963, Article 101963

2020

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Raman Spectroscopy Combined with Principal Component Analysis for Screening Nasopharyngeal Cancer in Human Blood Sera

Applied spectroscopy, 2017-11, Vol.71 (11), p.2497-2503

2017

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Analysis of tuberculosis disease through Raman spectroscopy and machine learning

Photodiagnosis and photodynamic therapy, 2018-12, Vol.24, p.286-291

2018

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An intrafamilial phenotypic variability in Ellis‐Van Creveld syndrome due to a novel 27 bps deletion mutation

American journal of medical genetics. Part A, 2021-10, Vol.185 (10), p.2888-2894

2021

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An intrafamilial phenotypic variability in Ellis‐Van Creveld syndrome due to a novel 27bps deletion mutation

American journal of medical genetics. Part A, 2021-10, Vol.185 (10), p.2888-2894

2021

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Efficient Production, Purification and Characterization of Therapeutically Significant L-Asparaginase from Bacillus licheniformis ASN51

Polish journal of environmental studies, 2023-01, Vol.32 (5), p.4267-4280

2023

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Diagnosis of thalassemia and iron deficiency anemia using confocal and atomic force microscopy

Laser physics letters, 2017-11, Vol.14 (11), p.115703

2017

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Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2

American journal of human genetics, 2016-02, Vol.98 (2), p.331-338

2016

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A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family

EJD. European journal of dermatology, 2018-04, Vol.28 (2), p.209-216

2018

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Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families

International journal of dermatology, 2017-12, Vol.56 (12), p.1406-1413

2017

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Plant beneficial endophytic bacteria: Mechanisms, diversity, host range and genetic determinants

Characterization and applications of glutaminase free L-asparaginase from indigenous Bacillus halotolerans ASN9

Antioxidants and Calcium Modulators Preclude in Vitro Hepatitis B Virus–Induced Mitochondrial Damage

A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis‐2 with impaired intellectual development

Restoration of IL-11 and IL-15 cytokine production post calcium modulators and ROS treatment can assist viral clearance both in vitro and in vivo

Effect of oxidative stress and calcium deregulation on FAM26F (CALHM6) expression during hepatitis B virus infection

CDKN2A/P16INK4A variants association with breast cancer and their in-silico analysis

Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny

L237P Substitution in the UROS Gene Causes X-linked Recessive Congenital Erythropoietic Porphyria in Pakistani Consanguineous Family Through Altered Uroporphyrinogen III Binding

Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities

Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families

Facile Synthesis as well as Structural, Raman, Dielectric and Antibacterial Characteristics of Cu Doped ZnO Nanoparticles

In silico Analysis of Candidate Genes Involved in Sanfilippo Syndrome

Structural and functional insights into a novel homozygous missense pathogenic variant in CUL7 identified in consanguineous Pakistani family

Demonstrating the application of Raman spectroscopy together with chemometric technique for screening of asthma disease

Cost effective and efficient screening of tuberculosis disease with Raman spectroscopy and machine learning algorithms

Raman Spectroscopy Combined with Principal Component Analysis for Screening Nasopharyngeal Cancer in Human Blood Sera

Analysis of tuberculosis disease through Raman spectroscopy and machine learning

An intrafamilial phenotypic variability in Ellis‐Van Creveld syndrome due to a novel 27 bps deletion mutation

An intrafamilial phenotypic variability in Ellis‐Van Creveld syndrome due to a novel 27bps deletion mutation

Efficient Production, Purification and Characterization of Therapeutically Significant L-Asparaginase from Bacillus licheniformis ASN51

Diagnosis of thalassemia and iron deficiency anemia using confocal and atomic force microscopy

Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2

A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family

Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families

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