- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Dissertation, 2020
- Schlagwort
-
Itching
Molecules
Genes
Identification
- Ereignis
-
Veröffentlichung
- (wo)
-
Erlangen
- (wer)
-
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (wann)
-
2021
- Urheber
- Beteiligte Personen und Organisationen
-
Kremer, Andreas
Feigenspan, Andreas
- URN
-
urn:nbn:de:bvb:29-opus4-147861
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:23 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Kühn, Helen
- Kremer, Andreas
- Feigenspan, Andreas
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Entstanden
- 2021
Ähnliche Objekte (12)
Kidney Itch
itchY
Psychogenic itch
In- and extrinsic signalling pathways modulating oligodendroglial migration
Pharmacology of itch
Complementary roles of murine NaV1.7, NaV1.8 and NaV1.9 in acute itch signalling
Inositol Pyrophosphates: Energetic, Omnipresent and Versatile Signalling Molecules
Sophorolipid inhibits histamine-induced itch by decreasing PLC/IP3R signaling pathway activation and modulating TRPV1 activity
Attentional processing of itch
Itch/β-arrestin2-dependent non-proteolytic ubiquitylation of SuFu controls Hedgehog signalling and medulloblastoma tumorigenesis
Distraction From Itch Shows Brainstem Activation Without Reduction in Experimental Itch Sensation
Expression of Hedgehog signalling molecules in microcystic adnexal carcinoma
Kidney Itch
itchY
Psychogenic itch
In- and extrinsic signalling pathways modulating oligodendroglial migration
Pharmacology of itch
Complementary roles of murine NaV1.7, NaV1.8 and NaV1.9 in acute itch signalling
Inositol Pyrophosphates: Energetic, Omnipresent and Versatile Signalling Molecules
Sophorolipid inhibits histamine-induced itch by decreasing PLC/IP3R signaling pathway activation and modulating TRPV1 activity
Attentional processing of itch
Itch/β-arrestin2-dependent non-proteolytic ubiquitylation of SuFu controls Hedgehog signalling and medulloblastoma tumorigenesis
Distraction From Itch Shows Brainstem Activation Without Reduction in Experimental Itch Sensation
Expression of Hedgehog signalling molecules in microcystic adnexal carcinoma
Kidney Itch
itchY
Psychogenic itch
In- and extrinsic signalling pathways modulating oligodendroglial migration
Pharmacology of itch
Complementary roles of murine NaV1.7, NaV1.8 and NaV1.9 in acute itch signalling
Inositol Pyrophosphates: Energetic, Omnipresent and Versatile Signalling Molecules
Sophorolipid inhibits histamine-induced itch by decreasing PLC/IP3R signaling pathway activation and modulating TRPV1 activity
Attentional processing of itch
Itch/β-arrestin2-dependent non-proteolytic ubiquitylation of SuFu controls Hedgehog signalling and medulloblastoma tumorigenesis
Distraction From Itch Shows Brainstem Activation Without Reduction in Experimental Itch Sensation