List of works - Danielle E. Dye

Actin mutations are one cause of congenital fibre type disproportion

scientific article published in November 2004

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

scientific article published on 30 March 2018

Bandstab: a PCR-based alternative to cloning PCR products

scientific article published on 01 April 1997

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

scientific article (publication date: July 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?

scientific article published in January 1999

Family data in Rett syndrome: association with other genetic disorders

scientific article

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.

scientific article published on 19 April 2014

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

scientific article published on 06 December 2019

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

scientific article published on June 2015

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

scientific article

Melanoma biomolecules: independently identified but functionally intertwined.

scientific article published on 24 September 2013

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 08 May 2006

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

scientific article published in July 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).

scientific article published on September 2006

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

scientific article published on 22 November 2016

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

scientific article

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

scientific article

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

scientific article

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

scientific article published in December 2010

The role of immunoglobulin superfamily cell adhesion molecules in cancer metastasis

scientific article

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

scientific article

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.

scientific article

List of works by 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.