I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Amiri‐yekta, Amir
92
results:
Search for persons
X
Format
Online (92)
Mediatypes
Articles (Online) (28)
OpenAccess-fulltext (64)
Sorted by: Relevance
Sorted by: Year
?
1
Whole genome sequencing identifies a homozygous splicing va..:
Amiri‐Yekta, Amir
;
Sen, Sharanya
;
Hazane‐Puch, Florence
...
Clinical Genetics. , 2024
Link:
https://doi.org/10.1111/..
?
2
CCDC65, encoding a component of the axonemal Nexin‐Dynein r..:
Jreijiri, Fadwa
;
Cavarocchi, Emma
;
Amiri‐Yekta, Amir
...
Clinical Genetics. , 2023
Link:
https://doi.org/10.1111/..
?
3
Whole exome sequencing of men with multiple morphological a..:
Kherraf, Zine‐Eddine
;
Cazin, Caroline
;
Coutton, Charles
...
Clinical Genetics. 96 (2019) 5 - p. 394-401 , 2019
Link:
https://doi.org/10.1111/..
?
4
PATL2 is a key actor of oocyte maturation whose invalidatio..:
Christou‐Kent, Marie
;
Kherraf, Zine‐Eddine
;
Amiri‐Yekta, Amir
...
EMBO Molecular Medicine. 10 (2018) 5 - p. , 2018
Link:
https://doi.org/10.15252..
?
5
SPINK2 deficiency causes infertility by inducing sperm defe..:
Kherraf, Zine‐Eddine
;
Christou‐Kent, Marie
;
Karaouzene, Thomas
...
EMBO Molecular Medicine. 9 (2017) 8 - p. 1132-1149 , 2017
Link:
https://doi.org/10.15252..
?
6
Lack of CCDC146, a ubiquitous centriole and microtubule-ass..:
Kherraf, Zine Eddine
;
Muroňová, Jana
;
Giordani, Elsa
...
eLife. 12 (2024) - p. , 2024
Link:
https://doi.org/10.7554/..
?
7
Lack of CCDC146, a ubiquitous centriole and microtubule-ass..:
Kherraf, Zine Eddine
;
Muroňová, Jana
;
Giordani, Elsa
...
eLife. 12 (2024) - p. , 2024
Link:
https://doi.org/10.7554/..
?
8
New Mutations in DNHD1 Cause Multiple Morphological Abnorma..:
Martinez, Guillaume
;
Barbotin, Anne-Laure
;
Cazin, Caroline
...
International Journal of Molecular Sciences. 24 (2023) 3 - p. 2559 , 2023
Link:
https://doi.org/10.3390/..
?
9
Novel axonemal protein ZMYND12 interacts with TTC29 and DNA..:
Martinez, Guillaume
;
Dacheux, Denis
;
Broster Reix, Christine E
...
eLife. 12 (2023) - p. , 2023
Link:
https://doi.org/10.7554/..
?
10
A heterozygous missense variant in DLX3 leads to uterine le..:
Saboori-Darabi, Samaneh
;
Carrera, Paola
;
Akbari, Arvand
...
Gene. 865 (2023) - p. 147292 , 2023
Link:
https://doi.org/10.1016/..
?
11
Genetic causes of macrozoospermia and proposal for an optim..:
Coudert, Alicia
;
Cazin, Caroline
;
Amiri-Yekta, Amir
...
Journal of Genetics and Genomics. 50 (2023) 7 - p. 536-540 , 2023
Link:
https://doi.org/10.1016/..
?
12
Novel axonemal protein ZMYND12 interacts with TTC29 and DNA..:
Martinez, Guillaume
;
Dacheux, Denis
;
Broster Reix, Christine E
...
eLife. 12 (2023) - p. , 2023
Link:
https://doi.org/10.7554/..
?
13
Direct visualization of pre-protamine 2 detects protamine a..:
Rezaei-Gazik, Maryam
;
Vargas, Alexandra
;
Amiri-Yekta, Amir
...
Molecular Human Reproduction. 28 (2022) 2 - p. , 2022
Link:
https://doi.org/10.1093/..
?
14
KH domain containing 3 like (KHDC3L) frame-shift mutation c..:
Fatemi, Nayeralsadat
;
Ray, Pierre F.
;
Ramezanali, Fariba
...
European Journal of Obstetrics & Gynecology and Reproductive Biology. 259 (2021) - p. 100-104 , 2021
Link:
https://doi.org/10.1016/..
?
15
A missense mutation in IFT74, encoding for an essential com..:
Lorès, Patrick
;
Kherraf, Zine-Eddine
;
Amiri-Yekta, Amir
...
Human Genetics. 140 (2021) 7 - p. 1031-1043 , 2021
Link:
https://doi.org/10.1007/..
1-15