E-LIB Suche - Ergebnisse für: Zenker, Martin

1

Assessment of gene–disease associations and recommendations..:

Revencu, Nicole ; Eijkelenboom, Astrid ; Bracquemart, Claire...
Orphanet Journal of Rare Diseases. 19 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

2

Extracranial Vascular Anomalies Driven by RAS/MAPK Variants..:

Schmidt, Vanessa F. ; Kapp, Friedrich G. ; Goldann, Constantin...
Journal of the American Heart Association. 13 (2024) 8 - p. , 2024

Link: https://doi.org/10.1161/..

3

Differential methylation of OPRK1 in borderline personality..:

Gescher, Dorothee Maria ; Schanze, Denny ; Vavra, Peter...
Molecular Psychiatry. , 2024

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

4

Transactivation of Met signaling by oncogenic Gnaq drives t..:

Mengoni, Miriam ; Braun, Andreas Dominik ; Seedarala, Sahithi...
Cancer Gene Therapy. 31 (2024) 6 - p. 884-893 , 2024

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

5

Krebserkrankungen bei Menschen mit einer Intelligenzminderu..:

Sappok, Tanja ; Kowalski, Christoph ; Zenker, Martin..
Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 67 (2024) 3 - p. 362-369 , 2024

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

6

Developmental effect of RASopathy mutations on neuronal net..:

Weiss, Eva-Maria ; Guhathakurta, Debarpan ; Petrušková, Aneta...
Frontiers in Cellular Neuroscience. 18 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

7

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes..:

Figueroa, Karla P. ; Gross, Caspar ; Buena-Atienza, Elena...
Nature Genetics. , 2024

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

8

Monogenic causes of severe fetal abnormalities leading to p..

lessons from Neu-Laxova syndrome

Abdelfattah, Fatima , 2023

Link: https://nbn-resolving.de..

9

Syndromic forms of congenital hyperinsulinism:

Zenker, Martin ; Mohnike, Klaus ; Palm, Katja
Frontiers in Endocrinology. 14 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

10

364 MUCOSAL MICROBIOME IS LINKED TO WORSE PROGNOSIS IN GAST..:

Lehr, Konrad ; Nikitina, Darja ; Vilchez-Vargas, Ramiro...
Gastroenterology. 164 (2023) 6 - p. S-65-S-66 , 2023

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

11

Happle‐Tinschert syndrome variable phenotype as part of the..:

Cano, Ramiro ; Abad, María Eugenia ; Schanze, Denny...
Pediatric Dermatology. 40 (2023) 4 - p. 691-694 , 2023

Link: https://doi.org/10.1111/..

12

Molecular and cellular evidence for the impact of a hypertr..:

Nakhaei-Rad, Saeideh ; Haghighi, Fereshteh ; Bazgir, Farhad...
Communications Biology. 6 (2023) 1 - p. , 2023

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

13

Bifidobacteria shape antimicrobial T-helper cell responses ..:

Vogel, Katrin ; Arra, Aditya ; Lingel, Holger...
Nature Communications. 14 (2023) 1 - p. , 2023

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

14

Biallelic inactivation of the NF1 tumour suppressor gene in..:

Ramamoorthy, Senthilkumar ; Lebrecht, Dirk ; Schanze, Denny...
British Journal of Haematology. 204 (2023) 2 - p. 595-605 , 2023

Link: https://doi.org/10.1111/..

15

C-terminal variants in CDC42 drive type I interferon-depend..:

Kapp, Friedrich G. ; Kretschmer, Stefanie ; Beckmann, Cora C.A....
Clinical Immunology. 256 (2023) - p. 109777 , 2023

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