Lista de obras - Weil D - Dominio Público Uruguay

A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.

artículo científico publicado en 2002

Accumulation of mature mRNA in the nuclear fraction of mammalian cells.

artículo científico publicado en 1999

CPEB interacts with an ovary-specific eIF4E and 4E-T in early Xenopus oocytes.

artículo científico publicado en 2007

CPEB1, a novel gene silenced in gastric cancer: a Drosophila approach.

artículo científico publicado en 2011

Comparative ultrastructure of CRM1-Nucleolar bodies (CNoBs), Intranucleolar bodies (INBs) and hybrid PML/p62 bodies uncovers new facets of nuclear body dynamic and diversity

artículo científico publicado en 2015

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

artículo científico publicado en 2011

Cytoplasmic organelles on the road to mRNA decay.

artículo científico

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.

artículo científico publicado en 2002

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.

artículo científico publicado en 2003

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

scientific journal article

Dual RNA Processing Roles of Pat1b via Cytoplasmic Lsm1-7 and Nuclear Lsm2-8 Complexes

artículo científico publicado en 2017

Expression of the Wilms' tumor suppressor gene, WT1, is upregulated by leukemia inhibitory factor and induces monocytic differentiation in M1 leukemic cells ⬇️

artículo científico publicado el 1 de febrero de 1998

GC content shapes mRNA storage and decay in human cells

artículo científico publicado en 2019

GW body disassembly triggered by siRNAs independently of their silencing activity.

artículo científico publicado en 2007

In vivo kinetics of mRNA splicing and transport in mammalian cells

artículo científico publicado en 2002

Induction of tumor necrosis factor-alpha and -beta and interferon-gamma mRNA by interleukin 2 in murine lymphocytic cell lines.

artículo científico publicado en 1988

Interactions in the network of Usher syndrome type 1 proteins

scientific journal article

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

artículo científico publicado en 2012

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.

artículo científico publicado en 2003

Mitochondria associate with P-bodies and modulate microRNA-mediated RNA interference.

artículo científico publicado en 2011

Multiple binding of repressed mRNAs by the P-body protein Rck/p54.

artículo científico publicado en 2012

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

scientific journal article

Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations

artículo científico publicado en 2002

P-Bodies: Cytosolic Droplets for Coordinated mRNA Storage

scientific article published on 13 June 2018

P-Body Purification Reveals the Condensation of Repressed mRNA Regulons

artículo científico publicado en 2017

P-bodies and mitochondria: which place in RNA interference?

artículo científico publicado en 2012

P-body assembly requires DDX6 repression complexes rather than decay or Ataxin2/2L complexes

artículo científico publicado en 2015

Pat1 RNA-binding proteins: Multitasking shuttling proteins

scientific article published on 24 June 2019

Predominant expression of murine Bmx tyrosine kinase in the granulo-monocytic lineage ⬇️

artículo científico publicado el 1 de diciembre de 1997

RNA is a critical element for the sizing and the composition of phase-separated RNA-protein condensates

artículo científico publicado en 2019

RNA processing is a limiting step for murine tumor necrosis factor beta expression in response to interleukin-2 ⬇️

artículo científico publicado el 1 de noviembre de 1990

Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation

scientific article published on 15 August 2019

Re-viewing the 3D Organization of mRNPs

artículo científico publicado en 2018

Regulation of pim and myb mRNA accumulation by interleukin 2 and interleukin 3 in murine hematopoietic cell lines

scientific article published on 01 November 1988

Role of p54 RNA helicase activity and its C-terminal domain in translational repression, P-body localization and assembly

artículo científico publicado en 2009

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

artículo científico publicado en 2004

Secretion of tumor necrosis factor-alpha by fresh human acute nonlymphoblastic leukemic cells: role in the disappearance of normal CFU-GM progenitors

artículo científico publicado en 1990

Targeting the kinesin Eg5 to monitor siRNA transfection in mammalian cells

artículo científico publicado en 2002

Tau/DDX6 interaction increases microRNA activity

artículo científico publicado en 2018

The DDX6-4E-T interaction mediates translational repression and P-body assembly

artículo científico publicado en 2016

The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules

artículo científico publicado en 2005

Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome

artículo científico publicado en 2007

Translationally repressed mRNA transiently cycles through stress granules during stress.

artículo científico publicado en 2008

Unravelling the ultrastructure of stress granules and associated P-bodies in human cells.

artículo científico publicado en 2009

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

artículo científico publicado en 2003

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

scientific journal article

What's new about tumor necrosis factors? Report on the fourth TNF International Congress

artículo científico publicado el 1 de mayo de 1992

[GW bodies and stress granules, two cytoplasmic structures for mRNA degradation and storage in mammalian cells]

scientific article published on 01 January 2007

[Mitochondria, microRNA and RNA interference]

artículo científico publicado en 2012

[P-bodies: microscopic droplets to store mRNAs encoding regulatory proteins]

artículo científico publicado en 2018

Lista de obras de Weil D

A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.

Accumulation of mature mRNA in the nuclear fraction of mammalian cells.

CPEB interacts with an ovary-specific eIF4E and 4E-T in early Xenopus oocytes.

CPEB1, a novel gene silenced in gastric cancer: a Drosophila approach.

Comparative ultrastructure of CRM1-Nucleolar bodies (CNoBs), Intranucleolar bodies (INBs) and hybrid PML/p62 bodies uncovers new facets of nuclear body dynamic and diversity

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

Cytoplasmic organelles on the road to mRNA decay.

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Dual RNA Processing Roles of Pat1b via Cytoplasmic Lsm1-7 and Nuclear Lsm2-8 Complexes

Expression of the Wilms' tumor suppressor gene, WT1, is upregulated by leukemia inhibitory factor and induces monocytic differentiation in M1 leukemic cells ⬇️

GC content shapes mRNA storage and decay in human cells

GW body disassembly triggered by siRNAs independently of their silencing activity.

In vivo kinetics of mRNA splicing and transport in mammalian cells

Induction of tumor necrosis factor-alpha and -beta and interferon-gamma mRNA by interleukin 2 in murine lymphocytic cell lines.

Interactions in the network of Usher syndrome type 1 proteins

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.

Mitochondria associate with P-bodies and modulate microRNA-mediated RNA interference.

Multiple binding of repressed mRNAs by the P-body protein Rck/p54.

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations

P-Bodies: Cytosolic Droplets for Coordinated mRNA Storage

P-Body Purification Reveals the Condensation of Repressed mRNA Regulons

P-bodies and mitochondria: which place in RNA interference?

P-body assembly requires DDX6 repression complexes rather than decay or Ataxin2/2L complexes

Pat1 RNA-binding proteins: Multitasking shuttling proteins

Predominant expression of murine Bmx tyrosine kinase in the granulo-monocytic lineage ⬇️

RNA is a critical element for the sizing and the composition of phase-separated RNA-protein condensates

RNA processing is a limiting step for murine tumor necrosis factor beta expression in response to interleukin-2 ⬇️

Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation

Re-viewing the 3D Organization of mRNPs

Regulation of pim and myb mRNA accumulation by interleukin 2 and interleukin 3 in murine hematopoietic cell lines

Role of p54 RNA helicase activity and its C-terminal domain in translational repression, P-body localization and assembly

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

Secretion of tumor necrosis factor-alpha by fresh human acute nonlymphoblastic leukemic cells: role in the disappearance of normal CFU-GM progenitors

Targeting the kinesin Eg5 to monitor siRNA transfection in mammalian cells

Tau/DDX6 interaction increases microRNA activity

The DDX6-4E-T interaction mediates translational repression and P-body assembly

The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules

Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome

Translationally repressed mRNA transiently cycles through stress granules during stress.

Unravelling the ultrastructure of stress granules and associated P-bodies in human cells.

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

What's new about tumor necrosis factors? Report on the fourth TNF International Congress

[GW bodies and stress granules, two cytoplasmic structures for mRNA degradation and storage in mammalian cells]

[Mitochondria, microRNA and RNA interference]

[P-bodies: microscopic droplets to store mRNAs encoding regulatory proteins]