E-LIB Suche - Ergebnisse für: Lorenz-Depiereux, B

1

Kartierung eines dritten Genlocus für familiäre hemiplegisc..:

Freilinger, T ; Eckstein, G ; Herzog, J...
Aktuelle Neurologie. 31 (2004) S 1 - p. , 2004

2

A point mutation in the Pdia6 gene results in loss of pancr..:

Chhabra, N.F ; Amend, A.-L ; Bastidas-Ponce, A...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molmet.2021.101334. , 2021

Link: https://push-zb.helmholt..

3

A novel homozygous variant in exon 10 of the GALNT3 gene ca..:

Dayal, D ; Gupta, S ; Kumar, R...
info:eu-repo/semantics/altIdentifier/doi/10.5582/irdr.2020.03084. , 2021

Link: https://push-zb.helmholt..

4

Regulatory myeloid cells paralyze T cells through cell-cell..:

Baumann, T ; Dunkel, A ; Schmid, C...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41590-020-0666-9. , 2020

Link: https://push-zb.helmholt..

5

Mitochondrial DNA mutation analysis from exome sequencing—A..:

Wagner, M ; Berutti, R ; Lorenz-Depiereux, B...
info:eu-repo/semantics/altIdentifier/doi/10.1002/jimd.12109. , 2019

Link: https://push-zb.helmholt..

6

The elevation of circulating fibroblast growth factor 23 wi..:

Pastor-Arroyo, E.M ; Gehring, N.H ; Krudewig, C...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.kint.2018.02.017. , 2018

Link: https://push-zb.helmholt..

7

The first Scube3 mutant mouse line with pleiotropic phenoty..:

Fuchs, H ; Sabrautzki, S ; Przemeck, G.K.H...
info:eu-repo/semantics/altIdentifier/doi/10.1534/g3.116.033670. , 2016

Link: https://push-zb.helmholt..

8

Exome sequencing identifies a nonsense mutation in Fam46a a..:

Diener, S ; Bayer, S ; Sabrautzki, S...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00335-016-9619-x. , 2016

Link: https://push-zb.helmholt..

9

Viable Ednra Y129F mice feature human mandibulofacial dysos..:

Sabrautzki, S ; Sandholzer, M.A ; Lorenz-Depiereux, B...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00335-016-9664-5. , 2016

Link: https://push-zb.helmholt..

10

Early onset hearing loss in autosomal recessive hypophospha..:

Steichen-Gersdorf, E ; Lorenz-Depiereux, B ; Strom, T.M.
info:eu-repo/semantics/altIdentifier/doi/10.1515/jpem-2014-0531. , 2015

Link: https://push-zb.helmholt..

11

An FGF23 missense mutation causes familial tumoral calcinos..:

Benet-Pagès, A ; Orlik, P ; Strom, T.M.
info:eu-repo/semantics/altIdentifier/doi/10.1093/hmg/ddi034. , 2005

Link: https://push-zb.helmholt..

12

The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene..:

White, Kenneth E. ; Jonsson, Kenneth B. ; Carn, Gwenaelle...
The Journal of Clinical Endocrinology & Metabolism. 86 (2001) 2 - p. 497-500 , 2001

Link: https://doi.org/10.1210/..

13

Depression and fatigue six months post-COVID-19 disease are..:

Weiß, Martin ; Gutzeit, Julian ; Appel, Katharina S....
Journal of Affective Disorders. 352 (2024) - p. 296-305 , 2024

Link: https://doi.org/10.1016/..

14

Comparison of post-COVID-19 symptoms in patients infected w..:

Hopff, Sina M. ; Appel, Katharina S. ; Miljukov, Olga...
Infection. , 2024

Link: https://doi.org/10.1007/..

15

Development of a long noncoding RNA-based machine learning ..:

Devaux, Yvan ; Zhang, Lu ; Lumley, Andrew I....
Nature Communications. 15 (2024) 1 - p. , 2024

Link: https://doi.org/10.1038/..