Emerging principles of primary cilia dynamics in controlling tissue organization and function

zu Verbundenen Objekten

Standort: Deutsche Nationalbibliothek Frankfurt am Main

Umfang: Online-Ressource

Sprache: Englisch

Erschienen in: In: The EMBO journal, 42 (2023), 21, e113891. https://doi.org/10.15252/embj.2023113891. ISSN: 1460-2075
In: The EMBO journal
In: 42
In: 21
In: 1460-2075

Ereignis: Veröffentlichung

(wo): Hohenheim

(wer): Universität Hohenheim

(wann): 2023

Urheber: Gopalakrishnan, Jayachandran
Feistel, Kerstin
Friedrich, Benjamin M.
Grapin‐Botton, Anne
Jurisch‐Yaksi, Nathalie
Mass, Elvira
Mick, David U.
Müller, Roman‐Ulrich
May‐Simera, Helen
Schermer, Bernhard
Schmidts, Miriam
Walentek, Peter
Wachten, Dagmar

DOI: 10.15252/embj.2023113891

URN: urn:nbn:de:101:1-2411130119420.175026050897

Rechteinformation: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Letzte Aktualisierung: 15.08.2025, 07:26 MESZ

Datenpartner

Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.

Original beim Datenpartner anzeigen

Beteiligte

Gopalakrishnan, Jayachandran
Feistel, Kerstin
Friedrich, Benjamin M.
Grapin‐Botton, Anne
Jurisch‐Yaksi, Nathalie
Mass, Elvira
Mick, David U.
Müller, Roman‐Ulrich
May‐Simera, Helen
Schermer, Bernhard
Schmidts, Miriam
Walentek, Peter
Wachten, Dagmar
Universität Hohenheim

Entstanden

2023

Ähnliche Objekte (12)

Hochschulschrift

Neph-Proteine interagieren mit dem Multiadapterprotein ZO-1

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy

The many faces of congenital anomalies of the kidney and urinary tract

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Ciliary dyneins and dynein related ciliopathies

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes

Identification of a TPP1 Q278X mutation in an iranian patient with neuronal ceroid lipofuscinosis 2: literature review and mutations update

Hochschulschrift

Neph-Proteine interagieren mit dem Multiadapterprotein ZO-1

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy

The many faces of congenital anomalies of the kidney and urinary tract

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Ciliary dyneins and dynein related ciliopathies

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes

Identification of a TPP1 Q278X mutation in an iranian patient with neuronal ceroid lipofuscinosis 2: literature review and mutations update

Hochschulschrift

Neph-Proteine interagieren mit dem Multiadapterprotein ZO-1

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy

The many faces of congenital anomalies of the kidney and urinary tract

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Ciliary dyneins and dynein related ciliopathies

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes

Identification of a TPP1 Q278X mutation in an iranian patient with neuronal ceroid lipofuscinosis 2: literature review and mutations update

Informationen zur Registrierung von Kultur- und Wissenseinrichtungen finden Sie hier.

Felder mit * müssen ausgefüllt werden.

Benutzername*

Bitte geben Sie Ihren Benutzernamen ein

E-Mail*

Bitte geben Sie Ihre E-Mail ein

Bitte füllen Sie dieses Feld nicht aus

Vorname

Nachname

Passwort*

Bitte geben Sie Ihr Passwort ein

Passwort bestätigen*

Bitte geben Sie das gleiche Passwort ein

Ich habe die Nutzungsbedingungen und die Datenschutzerklärung zur Erhebung persönlicher Daten gelesen und stimme ihnen zu. *

Dieses Feld ist ein Pflichtfeld.

Ich möchte den Newsletter der Deutschen Digitalen Bibliothek abonnieren. Siehe Informationen zum Newsletter-Abonnement.

Benutzerkonto angelegt

Ihr „Meine DDB“-Konto wurde erfolgreich angelegt. Bevor Sie sich in Ihrem Konto anmelden können, müssen Sie auf den Bestätigungslink in der Nachricht klicken, die wir gerade an die von Ihnen angegebene E-Mail-Adresse geschickt haben

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Angaben zum Objekt

Verweise und Beziehungen

Beteiligte, Orts- und Zeitangaben

Weitere Informationen

Datenpartner

Beteiligte

Entstanden

Ähnliche Objekte (12)

Neph-Proteine interagieren mit dem Multiadapterprotein ZO-1

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy

The many faces of congenital anomalies of the kidney and urinary tract

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Ciliary dyneins and dynein related ciliopathies

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes

Identification of a TPP1 Q278X mutation in an iranian patient with neuronal ceroid lipofuscinosis 2: literature review and mutations update

Neph-Proteine interagieren mit dem Multiadapterprotein ZO-1

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy

The many faces of congenital anomalies of the kidney and urinary tract

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Ciliary dyneins and dynein related ciliopathies

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes

Identification of a TPP1 Q278X mutation in an iranian patient with neuronal ceroid lipofuscinosis 2: literature review and mutations update

Neph-Proteine interagieren mit dem Multiadapterprotein ZO-1

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Emerging principles of primary cilia dynamics in controlling tissue organization and function

Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy

The many faces of congenital anomalies of the kidney and urinary tract

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Ciliary dyneins and dynein related ciliopathies

Recessive DNAH9 loss-of-function mutations cause laterality defects and subtle respiratory ciliary-beating defects

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes

Identification of a TPP1 Q278X mutation in an iranian patient with neuronal ceroid lipofuscinosis 2: literature review and mutations update

Verbundene Objekte

Passwort zurücksetzen