Suchergebnisse - "Hosseini, Seyedeh-Hanieh"

PubPharm (29)

1

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function

enthalten in: bioRxiv.org | 2024

von Dacheux, D. | Martinez, G. | Broster Reix, C. | +28

2

CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans

enthalten in: Clinical genetics | 2024

von Jreijiri, F. | Cavarocchi, E. | Amiri-Yekta, A. | +9

3

Evaluation of The 1499T>C Variant in The AKAP3 Gene of Infertile Men with Multiple Morphological Abnormalities of The Sperm Flagella Phenotype : A Case-Control Study

enthalten in: International journal of fertility & sterility | 2024

von Poursafari Talemi, E. | Hosseini, S. | Gourabi, H. | +2

4

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function

enthalten in: eLife | 2023

von Dacheux, D. | Martinez, G. | Broster Reix, C. | +29

5

New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella

enthalten in: International journal of molecular sciences | 2023

von Martinez, G. | Barbotin, A. | Cazin, C. | +14

6

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice

enthalten in: Journal of medical genetics | 2022

von Cong, J. | Wang, X. | Amiri-Yekta, A. | +18

7

A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome

enthalten in: Human genetics | 2021

von Lorès, P. | Kherraf, Z. | Amiri-Yekta, A. | +17

ErratumIn: Hum Genet. 2021 Mar 26;:. - PMID 33770252

8

Correction to : A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome

enthalten in: Human genetics | 2021

von Lorès, P. | Kherraf, Z. | Amiri-Yekta, A. | +17

ErratumFor: Hum Genet. 2021 Jul;140(7):1031-1043. - PMID 33689014

9

Observational retrospective study of Intracytoplasmic sperm injection outcomes of 117 infertile men with severe short tail sperm defect

enthalten in: Andrologia | 2021

von Hosseini, S. | Sabbaghian, M. | Mohseni Meybodi, A. | +2

10

Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome

enthalten in: Human genetics | 2021

von Lorès, P. | Kherraf, Z. | Amiri-Yekta, A. | +17