E-LIB Suche - Ergebnisse für: Mohammadi, Sanaz

1

A Comprehensive Overview of NF1 Mutations in Iranian Patien..:

Savad, Shahram ; Modarressi, Mohammad-Hossein ; Younesi, Sarang...
NeuroMolecular Medicine. 26 (2024) 1 - p. , 2024

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

2

Evaluation of silage maize production under pulsed drip irr..:

Mohammadi, Sanaz ; Mirlatifi, Seyed Majid ; Homaee, Mehdi..
Irrigation Science. 42 (2023) 2 - p. 269-283 , 2023

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

3

Association of Serum 25-Hydroxyvitamin D and Chronic Period..:

Shirmohammadi, Adileh ; Mohammadi, Sanaz ; Faramarzi, Masoumeh...
Frontiers in Dentistry. , 2023

Link: https://doi.org/10.18502..

4

A novel nonsense variant in the ATL3 gene is associated wit..:

Mohammadi, Sanaz ; Jafari Khamirani, Hossein ; Baneshi, Maryam...
Annals of Human Genetics. 87 (2023) 4 - p. 147-157 , 2023

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

5

Intronic OTOF mutation causes an atypical splicing defect r..:

Mohammadi, Sanaz ; Jafari Khamirani, Hossein ; Zoghi, Sina...
Journal of Genetics. 102 (2023) 1 - p. , 2023

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

6

Genotypic and phenotypic spectrum of Myofibrillar Myopathy ..:

Ehsani, Elham ; Khamirani, Hossein Jafari ; Abbasi, Zahra...
European Journal of Medical Genetics. 65 (2022) 8 - p. 104552 , 2022

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

7

The salivary exosomal microRNA as a potential biomarker in ..:

Safari, Zahra ; Firouzi, Alireza ; Rezaeikalantari, Nika...
Chemical Biology & Drug Design. 101 (2022) 5 - p. 1204-1215 , 2022

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

8

Signature pattern of gene expression and signaling pathway ..:

Ahmadloo, Salma ; Ling, King-Hwa ; Fazli, Ahmad...
Diabetology & Metabolic Syndrome. 14 (2022) 1 - p. , 2022

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

9

Latency-aware Topology Discovery in SDN-based Time-Sensitiv..:

, In: 2022 IEEE 8th International Conference on Network Softwarization (NetSoft),

Mohammadi, Sanaz ; Colle, Didier ; Tavernier, Wouter - p. 145-150 , 2022

Link: https://doi.org/10.1109/..

10

MCM2 mutation causes autosomal dominant nonsyndromic hearin..:

Zeraatpisheh, Zahra ; Sichani, Ali Saber ; Kamal, Neda...
Journal of Genetics. 101 (2022) 1 - p. , 2022

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

11

ZNF142 mutation causes neurodevelopmental disorder with spe..:

Kamal, Neda ; Khamirani, Hossein Jafari ; Mohammadi, Sanaz...
European Journal of Medical Genetics. 65 (2022) 7 - p. 104522 , 2022

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

12

Correction: A novel frameshift pathogenic variant in ST3GAL..:

Manoochehri, Jamal ; Dastgheib, Seyed Alireza ; Khamirani, Hossein Jafari...
Human Genome Variation. 8 (2021) 1 - p. , 2021

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

13

A novel PTRH2 missense mutation causing IMNEPD: a case repo..:

Khamirani, Hossein Jafari ; Zoghi, Sina ; Dianatpour, Mehdi...
Human Genome Variation. 8 (2021) 1 - p. , 2021

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

14

Exome sequencing identified a de novo frameshift pathogenic..:

Khamirani, Hossein Jafari ; Zoghi, Sina ; Sichani, Ali Saber...
Journal of Genetics. 100 (2021) 2 - p. , 2021

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

15

Perpetual Network Coding for Delay Sensitive Applications:

Mohammadi, Sanaz ; Pahlevani, Peyman ; Lucani, Daniel E.
Wireless Personal Communications. 120 (2021) 2 - p. 923-947 , 2021

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