E-LIB Suche - Ergebnisse für: Ariane Sadr Nabavi

1

The prevalence of SMN gene deletion/duplication in spinal m..:

Shariati, Mohammad ; Davoudi, Alireza ; Boostani, Reza...
Egyptian Journal of Medical Human Genetics. 25 (2024) 1 - p. , 2024

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

2

Copy number analysis from whole-exome sequencing data revea..:

Seyedtaghia, Mohammad Reza ; Soudyab, Mohammad ; Shariati, Mohammad...
Heliyon. 9 (2023) 4 - p. e15393 , 2023

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

3

Whole-Exome Sequencing Study of Consanguineous Parkinson's ..:

Soudyab, Mohammad ; Shariati, Mohammad ; Esfehani, Reza Jafarzadeh...
Journal of Molecular Neuroscience. 72 (2022) 12 - p. 2486-2496 , 2022

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

4

Cardiac Tamponade: A Rare Manifestation of Familial Mediter..:

Malek, Abdolreza ; Zeraati, Tina ; Sadr-Nabavi, Ariane...
Case Reports in Rheumatology. 2022 (2022) - p. 1-5 , 2022

Link: https://doi.org/10.1155/..

5

Exome sequencing identifies RASSF1 and KLK3 germline varian..:

Radmanesh, Hoda ; Liu, Di ; Geffers, Robert...
European Journal of Medical Genetics. 65 (2022) 3 - p. 104425 , 2022

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

6

AOPEP variants as a novel cause of recessive dystonia: Gene..:

Garavaglia, Barbara ; Vallian, Sadeq ; Romito, Luigi M....
Parkinsonism & Related Disorders. 97 (2022) - p. 52-56 , 2022

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

7

Developmental regulation and lateralization of N-methyl-d-a..:

Peyvandi Karizbodagh, Mostafa ; Sadr-Nabavi, Ariane ; Hami, Javad...
Neuropeptides. 89 (2021) - p. 102183 , 2021

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

8

Clinically relevant copy-number variants in exome sequencin..:

Zech, Michael ; Boesch, Sylvia ; Škorvánek, Matej...
Parkinsonism & Related Disorders. 84 (2021) - p. 129-134 , 2021

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

9

A review of Genetic Etiology and Emerging Molecular Therapi..:

Mohammad Reza Seyyed taghia ; Reza Jafarzadeh Esfehani ; Reza Boostani..
https://rcm.mums.ac.ir/article_18105_bb5add0c44a8170bb0fe6e734c973830.pdf. , 2021

Link: https://doi.org/10.22038..

10

Intellectual disability; an example of not relying on karyo..:

Khadivi zand, Farhad ; Shariati, Mohammad ; Sabeti Aghabozorgi, Amirsaeed...
Meta Gene. 24 (2020) - p. 100666 , 2020

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

11

PREVALENCE OF ß-THALASSEMIA MUTATIONS AMONG NORTHEASTERN IR..:

Jaripour, Mohammad Ehsan ; Hayatigolkhatmi, Kourosh ; Iranmanesh, Vahid...
Mediterranean Journal of Hematology and Infectious Diseases. 10 (2018) 1 - p. e2018042 , 2018

Link: https://doi.org/10.4084/..

12

Assessment of an APOBEC3B truncating mutation, c.783delG, i..:

Radmanesh, Hoda ; Spethmann, Tessa ; Enßen, Julia...
Breast Cancer Research and Treatment. 162 (2017) 1 - p. 31-37 , 2017

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

13

Evaluation of bax, bcl-2, p21 and p53 genes expression vari..:

Najmeh Ghatei ; Ariane Sadr Nabavi ; Mohammad Hossein Bahreyni Toosi...
http://ijbms.mums.ac.ir/article_9273_bc74d60d42db99a45d61a4081d29fd6a.pdf. , 2017

Link: https://doi.org/10.22038..

14

Diabetes in Pregnancy Adversely Affects the Expression of G..:

Hami, Javad ; Karimi, Razieh ; Haghir, Hossein..
Journal of Molecular Neuroscience. 57 (2015) 2 - p. 273-281 , 2015

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

15

The effects of maternal diabetes on expression of insulin-l..:

Hami, Javad ; Sadr-Nabavi, Ariane ; Sankian, Mojtaba..
Brain Structure and Function. 218 (2012) 1 - p. 73-84 , 2012

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