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
Bassam Abu-Libdeh
126
results:
Search for persons
X
Format
Online (126)
Mediatypes
Articles (Online) (81)
Bookchapter (Online) (12)
OpenAccess-fulltext (32)
Thesis (Online) (1)
Languages
german (1)
english (118)
Sorted by: Relevance
Sorted by: Year
?
1
GRID1/GluD1 homozygous variants linked to intellectual disa..:
Ung, Dévina C.
;
Pietrancosta, Nicolas
;
Badillo, Elena Baz
...
Molecular Psychiatry. 29 (2024) 4 - p. 1205-1215 , 2024
Link:
https://doi.org/10.1038/..
?
2
Unbiased phenotype and genotype matching maximizes gene dis..:
Rips, Jonathan
;
Halstuk, Orli
;
Fuchs, Adina
...
Genetics in Medicine. 26 (2024) 4 - p. 101068 , 2024
Link:
https://doi.org/10.1016/..
?
3
SLC4A10 mutation causes a neurological disorder associated ..:
Fasham, James
;
Huebner, Antje K
;
Liebmann, Lutz
...
Brain. 146 (2023) 11 - p. 4547-4561 , 2023
Link:
https://doi.org/10.1093/..
?
4
A loss-of-function mutation in human Oxidation Resistance 1..:
Lin, Xiaolin
;
Wang, Wei
;
Yang, Mingyi
...
Genome Biology. 24 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
5
A loss-of-function mutation in human Oxidation Resistance 1..:
Xiaolin Lin
;
Wei Wang
;
Mingyi Yang
...
https://doi.org/10.1186/s13059-023-03037-1. , 2023
Link:
https://doi.org/10.1186/..
?
6
Orbital nodular fasciitis in child with biallelic germline ..:
Rips, Jonathan
;
Abu-Libdeh, Bassam
;
Koplewitz, Benjamin Z.
...
European Journal of Medical Genetics. 65 (2022) 6 - p. 104513 , 2022
Link:
https://doi.org/10.1016/..
?
7
Replicative Stress Coincides with Impaired Nuclear DNA Dama..:
Douiev, Liza
;
Miller, Chaya
;
Keller, Guy
...
International Journal of Molecular Sciences. 23 (2022) 8 - p. 4149 , 2022
Link:
https://doi.org/10.3390/..
?
8
Glycogen Storage Disease type IA refractory to cornstarch: ..:
Steg Saban, Or
;
Pode-Shakked, Ben
;
Abu-Libdeh, Bassam
...
European Journal of Medical Genetics. 65 (2022) 6 - p. 104518 , 2022
Link:
https://doi.org/10.1016/..
?
9
RECON syndrome is a genome instability disorder caused by m..:
Abu-Libdeh, Bassam
;
Jhujh, Satpal S.
;
Dhar, Srijita
...
Journal of Clinical Investigation. 132 (2022) 5 - p. , 2022
Link:
https://doi.org/10.1172/..
?
10
Replicative Stress Coincides with Impaired Nuclear DNA Dama..:
Liza Douiev
;
Chaya Miller
;
Guy Keller
...
Molecular Pathology, Diagnostics, and Therapeutics. , 2022
Link:
https://doi.org/10.3390/..
?
11
RECON syndrome is a genome instability disorder caused by m..:
Bassam Abu-Libdeh
;
Satpal S. Jhujh
;
Srijita Dhar
...
https://doi.org/10.1172/JCI147301. , 2022
Link:
https://doaj.org/article..
?
12
Replicative Stress Coincides with Impaired Nuclear DNA Dama..:
Liza Douiev
;
Chaya Miller
;
Guy Keller
...
https://www.mdpi.com/1422-0067/23/8/4149. , 2022
Link:
https://doi.org/10.3390/..
?
13
Upregulation of COX4-2 via HIF-1α in Mitochondrial COX4-1 D..:
Douiev, Liza
;
Miller, Chaya
;
Ruppo, Shmuel
...
Cells. 10 (2021) 2 - p. 452 , 2021
Link:
https://doi.org/10.3390/..
?
14
PNC2 (SLC25A36) Deficiency Associated With the Hyperinsulin..:
Shahroor, Maher A
;
Lasorsa, Francesco M
;
Porcelli, Vito
...
The Journal of Clinical Endocrinology & Metabolism. 107 (2021) 5 - p. 1346-1356 , 2021
Link:
https://doi.org/10.1210/..
?
15
Homozygous variant in MADD, encoding a Rab guanine nucleoti..:
Abu-Libdeh, Bassam
;
Mor-Shaked, Hagar
;
Atawna, Amir A.
...
European Journal of Human Genetics. 29 (2021) 6 - p. 977-987 , 2021
Link:
https://doi.org/10.1038/..
1-15
