Correction: IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Correction: IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport ; volume:81 ; number:1 ; day:27 ; month:11 ; year:2024 ; pages:1 ; date:12.2024
Cellular and molecular life sciences ; 81, Heft 1 (27.11.2024), 1, 12.2024

Classification: Recht

Creator: Anitei, Mihaela
Bruno, Francesca
Valkova, Christina
Dau, Therese
Cirri, Emilio
Mestres, Iván
Calegari, Federico
Kaether, Christoph

Contributor: SpringerLink (Online service)

DOI: 10.1007/s00018-024-05508-5

URN: urn:nbn:de:101:1-2502122124335.548753701828

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:33 AM CEST

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Associated

Anitei, Mihaela
Bruno, Francesca
Valkova, Christina
Dau, Therese
Cirri, Emilio
Mestres, Iván
Calegari, Federico
Kaether, Christoph
SpringerLink (Online service)

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Correction: IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport

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Other Objects (12)

IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport

Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report

Golgi

Modeling cortical development and microcephaly in human pluripotent stem cells using combinatorial pathway inhibition

Characteristics of children of the Microcephaly Epidemic Research Group Pediatric Cohort who developed postnatal microcephaly

Zika Virus Infection, Pregnancy and Microcephaly

STIL balancing primary microcephaly and cancer

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Case Report: Prenatal Recurrent Microcephaly and Corpus Callosum Abnormalities in a Chinese Family with Novel Biallelic SASS6 Mutations

Molecular genetic and cytogenetic analyses of autosomal recessive primary microcephaly (MCPH) : mouse model, new locus and novel mutations

IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport

Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report

Golgi

Modeling cortical development and microcephaly in human pluripotent stem cells using combinatorial pathway inhibition

Characteristics of children of the Microcephaly Epidemic Research Group Pediatric Cohort who developed postnatal microcephaly

Zika Virus Infection, Pregnancy and Microcephaly

STIL balancing primary microcephaly and cancer

The Golgi apparatus

ULK1 phosphorylates Sec23A and mediates autophagy-induced inhibition of ER-to-Golgi traffic

Case Report: Prenatal Recurrent Microcephaly and Corpus Callosum Abnormalities in a Chinese Family with Novel Biallelic SASS6 Mutations

Molecular genetic and cytogenetic analyses of autosomal recessive primary microcephaly (MCPH) : mouse model, new locus and novel mutations

IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport

Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report

Golgi

Modeling cortical development and microcephaly in human pluripotent stem cells using combinatorial pathway inhibition

Characteristics of children of the Microcephaly Epidemic Research Group Pediatric Cohort who developed postnatal microcephaly

Zika Virus Infection, Pregnancy and Microcephaly

STIL balancing primary microcephaly and cancer

The Golgi apparatus

ULK1 phosphorylates Sec23A and mediates autophagy-induced inhibition of ER-to-Golgi traffic

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Molecular genetic and cytogenetic analyses of autosomal recessive primary microcephaly (MCPH) : mouse model, new locus and novel mutations

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