Lista de obras - Danielle E. Dye - Dominio Público Uruguay

Actin mutations are one cause of congenital fibre type disproportion

artículo científico publicado en 2004

Aged neutrophils accumulate in lymphoid tissues from healthy elderly mice and infiltrate T and B cell zones

artículo científico publicado en 2018

Bandstab: a PCR-based alternative to cloning PCR products

artículo científico publicado en 1997

Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter

artículo científico publicado en 1999

Dystrophin gene transcripts skipping the mdx mutation

article

Familial aggregation in Rett syndrome: what is the evidence for clustering of other disorders in families of affected girls?

artículo científico publicado en 1999

Family data in Rett syndrome: association with other genetic disorders

artículo científico publicado en 2000

Hereditary motor and sensory neuropathy – Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries

scientific article published on 01 December 2000

IL-2/CD40-activated macrophages rescue age and tumor-induced T cell dysfunction in elderly mice.

artículo científico publicado en 2014

In Vitro Expansion of Keratinocytes on Human Dermal Fibroblast-Derived Matrix Retains Their Stem-Like Characteristics

artículo científico publicado en 2019

Interactions between Skeletal Muscle Myoblasts and their Extracellular Matrix Revealed by a Serum Free Culture System.

artículo científico publicado en 2015

Lipid-laden partially-activated plasmacytoid and CD4(-)CD8α(+) dendritic cells accumulate in tissues in elderly mice

artículo científico publicado en 2014

Melanoma biomolecules: independently identified but functionally intertwined.

artículo científico

Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).

artículo científico publicado en 2009

Mutations in TPM3 are a common cause of congenital fiber type disproportion

artículo científico publicado en 2008

Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).

artículo científico publicado en 2004

Myosin storage (hyaline body) myopathy: a case report.

artículo científico publicado en 2006

Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred

artículo científico publicado en 2006

Patterns of pregnancy loss, perinatal mortality, and postneonatal childhood deaths in families of girls with Rett syndrome.

artículo científico publicado en 1999

Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?

scientific article published on 01 July 1997

Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1).

artículo científico publicado en 2006

Silk fibroin scaffolds with muscle-like elasticity support in vitro differentiation of human skeletal muscle cells.

artículo científico publicado en 2016

The Western Australian family connections genealogical project: detection of familial occurrences of single gene and chromosomal disorders

artículo científico publicado en 2014

The gene for the human Src-like adaptor protein (hSLAP) is located within the 64-kb intron of the thyroglobulin gene

artículo científico publicado en 1998

The impact of single gene and chromosomal disorders on hospital admissions in an adult population

artículo científico publicado en 2011

The impact of single gene and chromosomal disorders on hospital admissions of children and adolescents: a population-based study.

artículo científico publicado en 2010

The role of immunoglobulin superfamily cell adhesion molecules in cancer metastasis

artículo científico publicado en 2012

Using genetic epidemiology to study Rett syndrome: the design of a case-control study.

artículo científico publicado en 2000

WITHDRAWN: The Fundamental And Pathological Importance Of Oxysterol Binding Protein And Its Related Proteins

retracted scientific article published on 10 September 2018

hShroom1 links a membrane bound protein to the actin cytoskeleton.

artículo científico publicado en 2009

Lista de obras de Danielle E. Dye

Actin mutations are one cause of congenital fibre type disproportion

Aged neutrophils accumulate in lymphoid tissues from healthy elderly mice and infiltrate T and B cell zones

Bandstab: a PCR-based alternative to cloning PCR products

Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter

Dystrophin gene transcripts skipping the mdx mutation

Familial aggregation in Rett syndrome: what is the evidence for clustering of other disorders in families of affected girls?

Family data in Rett syndrome: association with other genetic disorders

Hereditary motor and sensory neuropathy – Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries

IL-2/CD40-activated macrophages rescue age and tumor-induced T cell dysfunction in elderly mice.

In Vitro Expansion of Keratinocytes on Human Dermal Fibroblast-Derived Matrix Retains Their Stem-Like Characteristics

Interactions between Skeletal Muscle Myoblasts and their Extracellular Matrix Revealed by a Serum Free Culture System.

Lipid-laden partially-activated plasmacytoid and CD4(-)CD8α(+) dendritic cells accumulate in tissues in elderly mice

Melanoma biomolecules: independently identified but functionally intertwined.

Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).

Mutations in TPM3 are a common cause of congenital fiber type disproportion

Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).

Myosin storage (hyaline body) myopathy: a case report.

Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred

Patterns of pregnancy loss, perinatal mortality, and postneonatal childhood deaths in families of girls with Rett syndrome.

Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?

Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1).

Silk fibroin scaffolds with muscle-like elasticity support in vitro differentiation of human skeletal muscle cells.

The Western Australian family connections genealogical project: detection of familial occurrences of single gene and chromosomal disorders

The gene for the human Src-like adaptor protein (hSLAP) is located within the 64-kb intron of the thyroglobulin gene

The impact of single gene and chromosomal disorders on hospital admissions in an adult population

The impact of single gene and chromosomal disorders on hospital admissions of children and adolescents: a population-based study.

The role of immunoglobulin superfamily cell adhesion molecules in cancer metastasis

Using genetic epidemiology to study Rett syndrome: the design of a case-control study.

WITHDRAWN: The Fundamental And Pathological Importance Of Oxysterol Binding Protein And Its Related Proteins

hShroom1 links a membrane bound protein to the actin cytoskeleton.