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Works matching AU Ranjzad, Fariba

Results: 4

1

Co-segregation of candidate polymorphism rs201204878 of the PKD1 gene in a large Iranian family with autosomal dominant polycystic disease.

Published in:

Experimental & Therapeutic Medicine, 2019, v. 18, n. 2, p. 1345, doi. 10.3892/etm.2019.7693

By:

Ranjzad, Fariba;
Tara, Ahmad;
Basiri, Abbas;
Aghdami, Nasser;
Moghadasali, Reza

Publication type:

Article

2

A common variant in the adiponectin gene and polycystic ovary syndrome risk.

Published in:

Molecular Biology Reports, 2012, v. 39, n. 3, p. 2313, doi. 10.1007/s11033-011-0981-1

By:

Ranjzad, Fariba;
Mahmoudi, Touraj;
Irani Shemirani, Atena;
Mahban, Aidin;
Nikzamir, Abdolrahim;
Vahedi, Mohsen;
Ashrafi, Mahnaz;
Gourabi, Hamid

Publication type:

Article

3

Influence of gene variants related to calcium homeostasis on biochemical parameters of women with polycystic ovary syndrome.

Published in:

Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 3, p. 225, doi. 10.1007/s10815-010-9506-4

By:

Ranjzad, Fariba;
Mahban, Aidin;
Irani Shemirani, Atena;
Mahmoudi, Touraj;
Vahedi, Mohsen;
Nikzamir, Abdolrahim;
Zali, Mohammad

Publication type:

Article

4

Identification of Three Novel Frameshift Mutations in the PKD1 Gene in Iranian Families with Autosomal Dominant Polycystic Kidney Disease Using Efficient Targeted Next-Generation Sequencing.

Published in:

Kidney & Blood Pressure Research, 2018, v. 43, n. 2, p. 471, doi. 10.1159/000488471

By:

Ranjzad, Fariba;
Aghdami, Nasser;
Tara, Ahmad;
Mohseni, Marzieh;
Moghadasali, Reza;
Basiri, Abbas

Publication type:

Article