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
Majmundar, Amar J
80
results:
Search for persons
X
Format
Online (80)
Mediatypes
Articles (Online) (26)
OpenAccess-fulltext (54)
Sorted by: Relevance
Sorted by: Year
?
1
Endothelial HIF-2α regulates murine pathological angiogenes..:
Skuli, Nicolas
;
Majmundar, Amar J.
;
Krock, Bryan L.
...
Journal of Clinical Investigation. 134 (2024) 8 - p. , 2024
Link:
https://doi.org/10.1172/..
?
2
Expanding the spectrum of novel candidate genes using trio ..:
Schneider, Ronen
;
Shril, Shirlee
;
Buerger, Florian
...
Genes & Diseases. , 2024
Link:
https://doi.org/10.1016/..
?
3
OXGR1 is a candidate disease gene for human calcium oxalate..:
Majmundar, Amar J.
;
Widmeier, Eugen
;
Heneghan, John F.
...
Genetics in Medicine. 25 (2023) 3 - p. 100351 , 2023
Link:
https://doi.org/10.1016/..
?
4
Activation of 2‐oxoglutarate receptor 1 (OXGR1) by α‐ketogl..:
Heneghan, John F.
;
Majmundar, Amar J.
;
Rivera, Alicia
...
Physiological Reports. 10 (2022) 14 - p. , 2022
Link:
https://doi.org/10.14814..
?
5
A Novel Form of Familial Vasopressin Deficient Diabetes Ins..:
Habiby, Reema
;
Bichet, Daniel G
;
Arthus, Marie-Francoise
...
The Journal of Clinical Endocrinology & Metabolism. 107 (2022) 6 - p. e2513-e2522 , 2022
Link:
https://doi.org/10.1210/..
?
6
Reverse phenotyping facilitates disease allele calling in e..:
Seltzsam, Steve
;
Wang, Chunyan
;
Zheng, Bixia
...
Genetics in Medicine. 24 (2022) 2 - p. 307-318 , 2022
Link:
https://doi.org/10.1016/..
?
7
Generation of Monogenic Candidate Genes for Human Nephrotic..:
Klämbt, Verena
;
Mao, Youying
;
Schneider, Ronen
...
Kidney International Reports. 6 (2021) 2 - p. 460-471 , 2021
Link:
https://doi.org/10.1016/..
?
8
Cystin genetic variants cause autosomal recessive polycysti..:
Yang, Chaozhe
;
Harafuji, Naoe
;
O'Connor, Amber K.
...
Scientific Reports. 11 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
9
A recurrent, homozygous EMC10 frameshift variant is associa..:
Shao, Diane D.
;
Straussberg, Rachel
;
Ahmed, Hind
...
Genetics in Medicine. 23 (2021) 6 - p. 1158-1162 , 2021
Link:
https://doi.org/10.1038/..
?
10
RecessiveNOS1APvariants impair actin remodeling and cause g..:
Majmundar, Amar J.
;
Buerger, Florian
;
Forbes, Thomas A.
...
Science Advances. 7 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1126/..
?
11
Recessive Mutations in SYNPO2 as a Candidate of Monogenic N..:
Mao, Youying
;
Schneider, Ronen
;
van der Ven, Peter F.M.
...
Kidney International Reports. 6 (2021) 2 - p. 472-483 , 2021
Link:
https://doi.org/10.1016/..
?
12
Sequencing the CaSR locus in Pakistani stone formers reveal..:
Ullah, Ihsan
;
Ottlewski, Isabel
;
Shehzad, Wasim
...
BMC Medical Genomics. 14 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
13
Mutations in transcription factor CP2-like 1 may cause a no..:
Klämbt, Verena
;
Werth, Max
;
Onuchic-Whitford, Ana C
...
Nephrology Dialysis Transplantation. 36 (2020) 2 - p. 237-246 , 2020
Link:
https://doi.org/10.1093/..
?
14
Gene panel sequencing identifies a likely monogenic cause i..:
Amar, Ali
;
Majmundar, Amar J.
;
Ullah, Ihsan
...
Human Genetics. 138 (2019) 3 - p. 211-219 , 2019
Link:
https://doi.org/10.1007/..
?
15
COL4A1 mutations as a potential novel cause of autosomal do..:
Kitzler, Thomas M.
;
Schneider, Ronen
;
Kohl, Stefan
...
Human Genetics. 138 (2019) 10 - p. 1105-1115 , 2019
Link:
https://doi.org/10.1007/..
1-15