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Ranjha Khan Selected Research

Dimauro disease

9/2021Targeted exome sequencing identified a novel frameshift variant in the PGAM2 gene causing glycogen storage disease type X.

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Ranjha Khan Research Topics

Disease

2Azoospermia
07/2022 - 01/2021
2Infertility (Sterility)
11/2021 - 01/2019
2Breast Neoplasms (Breast Cancer)
01/2021 - 07/2019
1Asthenozoospermia
05/2022
1Ciliary Motility Disorders (Primary Ciliary Dyskinesia)
05/2022
1Glycogen Storage Disease (Glycogenosis)
09/2021
1Dimauro disease
09/2021
1Carcinogenesis
01/2021
1Severe Acute Respiratory Syndrome
10/2020
1Hypokalemic Periodic Paralysis (Periodic Paralysis, Hypokalemic)
12/2019
1Paralysis (Palsy)
12/2019
1Hypogonadism (Hypergonadotropic Hypogonadism)
01/2019

Drug/Important Bio-Agent (IBA)

2Proteins (Proteins, Gene)FDA Link
01/2021 - 10/2020
1Eosine Yellowish-(YS) (Eosin)IBA
07/2022
1Hematoxylin (Haematoxylon)IBA
07/2022
1Dyneins (Dynein)IBA
05/2022
11,2- di- (4- sulfamidophenyl)- 4- butylpyrazolidine- 3,5- dione (DSB)IBA
11/2021
1Phosphoglycerate Mutase (Phosphoglyceromutase)IBA
09/2021
1cyclo(Arg-Pro) (CI 4)IBA
01/2021
1Biomarkers (Surrogate Marker)IBA
01/2021
1Nonsense Codon (Nonsense Mutation)IBA
01/2021
1PotassiumIBA
12/2019
1Cyclin-Dependent Kinase Inhibitor p16IBA
07/2019
1Gonadotropin-Releasing Hormone (GnRH)FDA Link
01/2019