Detailansicht

Wissensnetz

Person

Brunhilde Wirth

Biologin

Name	Brunhilde Wirth
Ort	Deutschland
Geschlecht	weiblich
Akademischer Grad bzw. Titel	Prof. Dr. rer. nat.
Beruf	Biologin (charakteristischer Beruf) Hochschullehrerin
Variante	B. Wirth
Beziehung	Institut für Humangenetik (Köln) (Direktorin) Universitätsklinikum Köln
Quelle	Homepage: http://humangenetik.uk-koeln.de/das-institut (Stand: 04.11.2019)
Datensatztyp	Person
GND-Nummer	1198698098
Datensatz-ID	1198698098
Beteiligt an alle anzeigen Altered mitochondrial function in fibroblast cell lines derived from disease carriers of spinal muscular atrophy MAGED2: the gene associated with Bartter syndrome type 5 is a key regulator of Gαs signalling in the developing kidney Autophagy regulates neuronal excitability by controlling cAMP/protein kinase A signaling at the synapse CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia Cathepsin D as biomarker in CSF of nusinersen‐treated patients with spinal muscular atrophy Epigenetic regulation of PLS3 by the macrosatellite DXZ4 and the transcriptional regulator CHD4 Plastin 3 in health and disease: a matter of balance Mitochondrial defects in the respiratory complex I contribute to impaired translational initiation via ROS and energy homeostasis in SMA motor neurons Diagnosis and management of spinal muscular atrophy : : Part 2

Hinweis

Die Betaversion beinhaltet noch nicht alle Funktionen und Informationen des Katalogs des DNB-Portals. Falls Sie Informationen vermissen oder ein Medium bestellen wollen, besuchen Sie bitte die entsprechende Seite im Katalog des DNB-Portals über folgenden Link:

Katalog der Deutschen Nationalbibliothek

Brunhilde Wirth

Altered mitochondrial function in fibroblast cell lines derived from disease carriers of spinal muscular atrophy

MAGED2: the gene associated with Bartter syndrome type 5 is a key regulator of Gαs signalling in the developing kidney

Autophagy regulates neuronal excitability by controlling cAMP/protein kinase A signaling at the synapse

CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia

CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia

Cathepsin D as biomarker in CSF of nusinersen‐treated patients with spinal muscular atrophy

Epigenetic regulation of PLS3 by the macrosatellite DXZ4 and the transcriptional regulator CHD4

Plastin 3 in health and disease: a matter of balance

Mitochondrial defects in the respiratory complex I contribute to impaired translational initiation via ROS and energy homeostasis in SMA motor neurons

Diagnosis and management of spinal muscular atrophy : : Part 2