Lista de obras - Andreas Zimmer - Dominio Público Uruguay

A uniquely high number offtsZ genes in the mossPhyscomitrella patens

article

An ancient genome duplication contributed to the abundance of metabolic genes in the moss Physcomitrella patens

artículo científico publicado en 2007

Dating the early evolution of plants: detection and molecular clock analyses of orthologs.

artículo científico publicado en 2007

Erratum to: An ancient genome duplication contributed to the abundance of metabolic genes in the moss Physcomitrella patens

artículo científico publicado en 2016

Exploring plant biodiversity: the Physcomitrella genome and beyond.

artículo científico publicado en 2008

Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4

artículo científico publicado en 2019

Identification and characterization of NAGNAG alternative splicing in the moss Physcomitrella patens

artículo científico publicado en 2010

Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis

artículo científico publicado en 2017

Insights from the cold transcriptome of Physcomitrella patens: global specialization pattern of conserved transcriptional regulators and identification of orphan genes involved in cold acclimation

artículo científico publicado en 2014

Large impact of the apoplast on somatic embryogenesis in Cyclamen persicum offers possibilities for improved developmental control in vitro

artículo científico publicado en 2010

Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia

scientific article published on 30 September 2018

Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans

artículo científico publicado en 2017

Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome

artículo científico publicado en 2016

Reannotation and extended community resources for the genome of the non-seed plant Physcomitrella patens provide insights into the evolution of plant gene structures and functions

artículo científico publicado en 2013

Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

artículo científico publicado en 2017

Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosis

scientific article published on 26 September 2019

Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients

artículo científico publicado en 2016

Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in protein kinase D1

artículo científico publicado en 2020

The P. patens chromosome-scale assembly reveals moss genome structure and evolution. ⬇️

artículo científico publicado en 2017

The Position of Targeted Next-generation Sequencing in Epidermo-lysis Bullosa Diagnosis

artículo científico publicado en 2017

The Selaginella genome identifies genetic changes associated with the evolution of vascular plants

artículo científico publicado en 2011

Whole-Exome-Sequencing Reveals Small Deletions in CASP14 in Patients with Autosomal Recessive Inherited Ichthyosis

artículo científico publicado en 2016

Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome

artículo científico publicado en 2015

ppdb: plant promoter database version 3.0.

artículo científico publicado en 2013

Lista de obras de Andreas Zimmer

A uniquely high number offtsZ genes in the mossPhyscomitrella patens

An ancient genome duplication contributed to the abundance of metabolic genes in the moss Physcomitrella patens

Dating the early evolution of plants: detection and molecular clock analyses of orthologs.

Erratum to: An ancient genome duplication contributed to the abundance of metabolic genes in the moss Physcomitrella patens

Exploring plant biodiversity: the Physcomitrella genome and beyond.

Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4

Identification and characterization of NAGNAG alternative splicing in the moss Physcomitrella patens

Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis

Insights from the cold transcriptome of Physcomitrella patens: global specialization pattern of conserved transcriptional regulators and identification of orphan genes involved in cold acclimation

Large impact of the apoplast on somatic embryogenesis in Cyclamen persicum offers possibilities for improved developmental control in vitro

Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia

Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans

Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome

Reannotation and extended community resources for the genome of the non-seed plant Physcomitrella patens provide insights into the evolution of plant gene structures and functions

Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosis

Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients

Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in protein kinase D1

The P. patens chromosome-scale assembly reveals moss genome structure and evolution. ⬇️

The Position of Targeted Next-generation Sequencing in Epidermo-lysis Bullosa Diagnosis

The Selaginella genome identifies genetic changes associated with the evolution of vascular plants

Whole-Exome-Sequencing Reveals Small Deletions in CASP14 in Patients with Autosomal Recessive Inherited Ichthyosis

Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome

ppdb: plant promoter database version 3.0.