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Academic Journal

Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells

Subjects: ddc:570

  • Source: Stouffer MA, Khalaf-Nazzal R, Cifuentes-Diaz C, et al. Doublecortin mutation leads to persistent defects in the Golgi apparatus and

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Academic Journal

Insights into the localization and function of the membrane trafficking regulator GNOM ARF-GEF at the Golgi apparatus in Arabidopsis

  • Source: Naramoto S, Otegui M, Kutsuna N, et al. Insights into the localization and function of the membrane trafficking regulator GNOM ARF-GEF at the Golgi

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Academic Journal

MON-2, a Golgi protein, promotes longevity by upregulating autophagy through mediating inter-organelle communications

  • Source: Artan M, Sohn J, Lee C, Park SY, Lee SJV. MON-2, a Golgi protein, promotes longevity by upregulating autophagy through mediating inter-organelle communications.

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Academic Journal

MON-2, a Golgi protein, promotes longevity by upregulating autophagy through mediating inter-organelle communications

  • Source: Artan M, Sohn J, Lee C, Park SY, Lee SJV. MON-2, a Golgi protein, promotes longevity by upregulating autophagy through mediating inter-organelle communications.

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Academic Journal

Developmental patterning function of GNOM ARF-GEF mediated from the cell periphery

Subjects: General Immunology and Microbiology; General Biochemistry; Genetics and Molecular Biology

  • Source: Adamowski M, Matijevic I, Friml J. Developmental patterning function of GNOM ARF-GEF mediated from the cell periphery. eLife . 2024;13. doi: 10.7554/elife.68993

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Academic Journal

Developmental patterning function of GNOM ARF-GEF mediated from the cell periphery

Subjects: General Immunology and Microbiology; General Biochemistry; Genetics and Molecular Biology

  • Source: Adamowski M, Matijevic I, Friml J. Developmental patterning function of GNOM ARF-GEF mediated from the cell periphery. eLife . 2024;13. doi: 10.7554/elife.68993

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Academic Journal

A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features

  • Source: Marin Valencia I, Novarino G, Johansen A, et al. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features.

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Academic Journal

A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features

  • Source: Marin Valencia I, Novarino G, Johansen A, et al. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features.

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Academic Journal

BEX1/ARF1A1C is required for BFA-sensitive recycling of PIN auxin transporters and auxin-mediated development in arabidopsis

Subjects: ddc:570

  • Source: Tanaka H, Nodzyński T, Kitakura S, et al. BEX1/ARF1A1C is required for BFA-sensitive recycling of PIN auxin transporters and auxin-mediated development in arabidopsis. Plant and Cell Physiology .

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