Tayyaba Ishaq, BS, MPhil
Postdoctoral AssociateAbout
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Titles
Postdoctoral Associate
Biography
During M.Phil. she explored the Genetics of skeletal dysplasia along with purification of a human protein by nickel chromatography. Before joining the current position she is a Ph.D. student in School of Biological Sciences University of the Punjab Lahore, Pakistan working under the supervision of Professor Sadaf Naz on genetics of skeletal dysplasia.
In the current position she is working for purification of different biologics ENPP1 (a crucial enzyme that regulates ectopic calcification and bone mineralization), DNase1 (for the treatment of pathologies associate with the aberrant formation of neutrophil extracellular traps, or netosis) and an antigen MPO (for production of antibodies in mice) on large scale along with working on CKD murine model (Chronic kidney disease).
Departments & Organizations
Education & Training
- MPhil
- University of the Punjab Lahore, Pakisan, Human genetics (2017)
- BS
- MMG, University of the Punjab Lahore Pakistan, Microbiology and Molecular genetics (2015)
Research
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Overview
Medical Research Interests
- View Lab Website
BRADDOCK LAB
Research at a Glance
Publications Timeline
Publications
2022
Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia.
Reilly ML, Ain NU, Muurinen M, Tata A, Huber C, Simon M, Ishaq T, Shaw N, Rusanen S, Pekkinen M, Högler W, Knapen MFCM, van den Born M, Saunier S, Naz S, Cormier-Daire V, Benmerah A, Makitie O. Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia. Journal Of Bone And Mineral Research : The Official Journal Of The American Society For Bone And Mineral Research 2022, 37: 1642-1652. PMID: 35748595, PMCID: PMC9545074, DOI: 10.1002/jbmr.4639.Peer-Reviewed Original Research
2021
Novel form of rhizomelic skeletal dysplasia associated with a homozygous variant in GNPNAT1.
Ain NU, Baroncelli M, Costantini A, Ishaq T, Taylan F, Nilsson O, Mäkitie O, Naz S. Novel form of rhizomelic skeletal dysplasia associated with a homozygous variant in GNPNAT1. Journal Of Medical Genetics 2021, 58: 351-356. PMID: 32591345, DOI: 10.1136/jmedgenet-2020-106929.Peer-Reviewed Original Research
2020
RIN2 and BBS7 variants as cause of a coincidental syndrome.
Shaukat M, Ishaq T, Muhammad N, Naz S. RIN2 and BBS7 variants as cause of a coincidental syndrome. European Journal Of Medical Genetics 2020, 63: 103755. PMID: 31521835, DOI: 10.1016/j.ejmg.2019.103755.Peer-Reviewed Original Research
2018
Risk assessment and biofilm formation of bacterial communities associated with drinking water distribution system
T. Ishaq and B. Ali* DOI: 10.22438/jeb/39/5/MRN-713Peer-Reviewed Original Research In Press
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