Zihni E. Taskiran
Ankara, Turkey
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
De Novo Cloning and Functional Characterization of a Mechanosensitive Piezo-Like Ion Channel in the Crayfish.
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Published: June 26, 2023
Phenotypic and Genetic Features that Differ Between Hereditary and Sporadic Melanoma: Results of a Preliminary Study from a Single Center from Turkey.
Journal: Dermatology practical & conceptual
Published: January 12, 2023
Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3.
Journal: Human mutation
Published: February 21, 2022
The rare reason of pain in hip girdle: Mucolipidosis type 3 gamma.
Journal: The Turkish journal of pediatrics
Published: January 13, 2022
A novel mutation of keratin 5 in epidermolysis bullosa simplex with migratory circinate erythema.
Journal: Pediatric dermatology
Published: January 23, 2020
Primary tumor resection for initially staged IV breast cancer: An emphasis on programmed death-ligand 1 expression, promoter methylation status, and survival.
Journal: Medicine
Published: August 16, 2019
Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing.
Journal: Fetal and pediatric pathology
Published: July 16, 2019
Identification of two novel PNPLA1 mutations in Turkish families with autosomal recessive congenital ichthyosis.
Journal: The Turkish journal of pediatrics
Published: January 01, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026