Suchergebnisse - "Kherraf, Zine-Eddine"

PubPharm (74)

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

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse

enthalten in: eLife | 2024

von Muroňová, J. | Kherraf, Z. | Giordani, E. | +26

3

A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility

enthalten in: Clinical genetics | 2024

von Kherraf, Z. | Barbotin, A. | Martinez, G. | +8

4

A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility

enthalten in: Clinical Genetics | 2024

von Kherraf, Z. | Barbotin, A. | Martinez, G. | +8

5

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse

enthalten in: bioRxiv.org | 2023

von Muroňová, J. | Kherraf, Z. | Giordani, E. | +26

6

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

7

Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy

enthalten in: Reproductive biomedicine online | 2023

von Boursier, A. | Boudry, A. | Mitchell, V. | +16

8

Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans

enthalten in: iScience | 2023

von Cavarocchi, E. | Sayou, C. | Lorès, P. | +12

9

Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters

enthalten in: Journal of genetics and genomics = Yi chuan xue bao | 2023

von Coudert, A. | Cazin, C. | Amiri-Yekta, A. | +40

10

Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort

enthalten in: Cancers | 2023

von Bouras, A. | Guidara, S. | Leone, M. | +13

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