E-LIB Suche - Ergebnisse für: DEHGHANI, MOHAMMADREZA

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

Novel nucleotide variations in the thrombomodulin (THBD) ge..:

Heidari, Mohammad Mehdi ; Mazrouei, Bahareh ; Tahmasebi, Maryam...
Gene. 895 (2024) - p. 148011 , 2024

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

3

Aetiology, risk factors and treatment of typical and atypic..:

Dehghani, Mohammadreza ; Pourmontaseri, Hossein
International Wound Journal. 21 (2024) 3 - p. , 2024

Link: https://doi.org/10.1111/..

4

Integrated whole transcriptome profiling revealed a convolu..:

Mollanoori, Hasan ; Ghelmani, Yaser ; Hassani, Bita.
Scientific Reports. 14 (2024) 1 - p. , 2024

Link: https://doi.org/10.1038/..

5

Robot-mounted sensing and local calibration for high-accura..:

Dehghani, Mohammadreza ; McKenzie, Ryan A. ; Irani, Rishad A..
Robotics and Computer-Integrated Manufacturing. 79 (2023) - p. 102429 , 2023

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

6

Investigating the impacts of socio-economic vulnerability i..:

Fatemi, Farin ; Fallah-Aliabadi, Saeed ; Sarsangi, Alireza..
International Journal of Disaster Risk Reduction. 91 (2023) - p. 103676 , 2023

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

7

Biallelic variants in ZNF142 lead to a syndromic neurodevel..:

Christensen, Maria B. ; Levy, Amanda M. ; Mohammadi, Nazanin A....
Clinical Genetics. 102 (2022) 2 - p. 98-109 , 2022

Link: https://doi.org/10.1111/..

8

Novel variants underlying autosomal recessive neurodevelopm..:

Moudi, Mahdiyeh ; Vahidi Mehrjardi, Mohammad Yahya ; Hozhabri, Hossein...
Journal of Clinical Laboratory Analysis. 36 (2022) 2 - p. , 2022

Link: https://doi.org/10.1002/..

9

Evaluation of the relationship between miR-337-3p and RAP1A..:

Dehghanian, Mehran ; Yarahmadi, Ghafour ; Fazeli, Javad...
Journal of Endometriosis and Pelvic Pain Disorders. 14 (2022) 4 - p. 178-182 , 2022

Link: https://doi.org/10.1177/..

10

Co-segregation of variant NSUN2 Lue198Arg among Iranian fam..:

Moudi, Mahdiyeh ; Vahidi Mehrjardi, Mohammad Yahya ; Kalantar, Seyed Mehdi...
Egyptian Journal of Medical Human Genetics. 23 (2022) 1 - p. , 2022

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

11

Bi-allelic loss-of-function variants in BCAS3 cause a syndr..:

Hengel, Holger ; Hannan, Shabab B. ; Dyack, Sarah...
The American Journal of Human Genetics. 108 (2021) 6 - p. 1069-1082 , 2021

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

12

Defective phosphatidylethanolamine biosynthesis leads to a ..:

Kaiyrzhanov, Rauan ; Wortmann, Saskia ; Reid, Taryn...
Brain. 144 (2021) 3 - p. e30-e30 , 2021

Link: https://doi.org/10.1093/..

13

Evaluation of miR-181b and miR-126-5p expression levels in ..:

Dehghani, Mohammadreza ; Aghaei Zarch, Seyed Mohsen ; Vahidi Mehrjardi, Mohammad Yahya...
Endocrinología, Diabetes y Nutrición (English ed.). 67 (2020) 7 - p. 454-460 , 2020

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

14

Martsolf syndrome with novel mutation in the TBC1D20 gene i..:

Hozhabri, Hossein ; Talebi, Mehrdad ; Mehrjardi, Mohammad Y. V...
American Journal of Medical Genetics Part A. 182 (2020) 5 - p. 957-961 , 2020

Link: https://doi.org/10.1002/..

15

Pontocerebellar hypoplasia due to bi-allelic variants in MI..:

Appelhof, Bart ; Wagner, Matias ; Hoefele, Julia...
European Journal of Human Genetics. 29 (2020) 3 - p. 411-421 , 2020

Link: https://doi.org/10.1038/..