E-LIB Suche - Ergebnisse für: Masoud Tajamolian

1

The association of RBX1 and BAMBI gene expression with oocy..:

Monshizadeh, Kimia ; Tajamolian, Masoud ; Anbari, Fatemeh...
BMC Medical Genomics. 17 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

2

The Effect of Angiotensin-Converting Enzyme Insertion/Delet..:

Samet, Mohammad ; Yazdi, Mehran ; Tajamolian, Masoud...
Biochemical Genetics. , 2023

Link: https://doi.org/10.1007/..

3

A Rare Missense Mutation and a Polymorphism with High Frequ..:

Yazd, EhsanFarashahi ; Tajamolian, Masoud ; Kolahdouz, Parisa...
Advanced Biomedical Research. 7 (2018) 1 - p. 37 , 2018

Link: https://doi.org/10.4103/..

4

Potential role of gender specific effect of leptin receptor..:

Dehghani, Mohammad Reza ; Mehrjardi, Mohammad Yahya Vahidi ; Dilaver, Nafi...
European Journal of Medical Genetics. 61 (2018) 8 - p. 465-467 , 2018

Link: https://doi.org/10.1016/..

5

Pitfalls in molecular diagnosis of 21-hydroxylase deficienc..:

Khanahmad, Hossein ; Kolahdouz, Mahsa ; Mohammadi, Zahra..
Advanced Biomedical Research. 4 (2015) 1 - p. 189 , 2015

Link: https://doi.org/10.4103/..

6

The rs3917779 polymorphism of P-selectin's significant asso..:

Kolahdouz, Parisa ; Farashahi Yazd, Ehsan ; Tajamolian, Masoud..
Graefe's Archive for Clinical and Experimental Ophthalmology. 253 (2015) 11 - p. 1967-1972 , 2015

Link: https://doi.org/10.1007/..

7

The association of RBX1 and BAMBI gene expression with oocy..:

Kimia Monshizadeh ; Masoud Tajamolian ; Fatemeh Anbari...
https://doi.org/10.1186/s12920-024-01800-2. , 2024

Link: https://doi.org/10.1186/..

8

A Rare Missense Mutation and a Polymorphism with High Frequ..:

Masoud Tajamolian ; Parisa Kolahdouz ; Parvaneh Nikpour...
http://www.advbiores.net/article.asp?issn=2277-9175;year=2018;volume=7;issue=1;spage=37;epage=37;aulast=Tajamolian. , 2018

Link: https://doi.org/10.4103/..

9

A Rare Missense Mutation and a Polymorphism with High Frequ..:

Tajamolian, Masoud ; Kolahdouz, Parisa ; Nikpour, Parvaneh...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841003/. , 2018

Link: http://www.ncbi.nlm.nih...

10

Pitfalls in molecular diagnosis of 21-hydroxylase deficienc..:

Kolahdouz, Mahsa ; Mohammadi, Zahra ; Kolahdouz, Parisa..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617158/. , 2015

Link: http://www.ncbi.nlm.nih...