Lista de obras - Sigmar Stricker - Dominio Público Uruguay

A Novel Role for the BMP Antagonist Noggin in Sensitizing Cells to Non-canonical Wnt-5a/Ror2/Disheveled Pathway Activation

artículo científico publicado en 2017

A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E.

artículo científico publicado en 2009

A comparative analysis of Meox1 and Meox2 in the developing somites and limbs of the chick embryo.

artículo científico publicado en 2007

A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C.

artículo científico publicado en 2010

A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model

artículo científico publicado en 2017

A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes

artículo científico publicado en 2009

A misplaced lncRNA causes brachydactyly in humans

artículo científico publicado en 2012

A molecular pathogenesis for transcription factor associated poly-alanine tract expansions

artículo científico publicado en 2004

A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range.

artículo científico publicado en 2009

A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution

artículo científico publicado en 2003

Abalone (Haliotis tuberculata) hemocyanin type 1 (HtH1) . Organization of the = 400 kDa subunit, and amino acid sequence of its functional units f, g and h

artículo científico publicado en 1999

Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders

artículo científico publicado en 2008

Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2

artículo científico publicado en 2005

An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression

artículo científico publicado en 2005

BMP signaling controls muscle mass

scientific journal article

Cell autonomous requirement of neurofibromin (Nf1) for postnatal muscle hypertrophic growth and metabolic homeostasis

artículo científico publicado en 2020

Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome.

artículo científico publicado en 2006

Comparative expression pattern of Odd-skipped related genes Osr1 and Osr2 in chick embryonic development

artículo científico publicado en 2006

Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation.

artículo científico publicado en 2009

Cooperation of BMP and IHH signaling in interdigital cell fate determination.

artículo científico publicado en 2018

Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis

artículo científico publicado en 2010

Corrigendum to “Mammalian mitochondrial nitric oxide synthase: Characterization of a novel candidate” [FEBS Lett. 580 (2006) 455-462]

scholarly article published in FEBS Letters

Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion.

artículo científico publicado en 2011

Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia.

artículo científico publicado en 2009

Editorial: Signaling Pathways in Embryonic Development

artículo científico publicado en 2017

Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit

artículo científico publicado en 2006

Evolution of a core gene network for skeletogenesis in chordates

artículo científico publicado en 2008

Expression of galectin-3 in skeletal tissues is controlled by Runx2.

artículo científico publicado en 2003

Expression of type XXIII collagen mRNA and protein

artículo científico publicado en 2006

FGF and ROR2 receptor tyrosine kinase signaling in human skeletal development

artículo científico

Faulty initiation of proteoglycan synthesis causes cardiac and joint defects

artículo científico publicado en 2011

Genome-wide strategies identify downstream target genes of connective tissue-associated transcription factors

artículo científico publicado en 2018

IRS4, a novel modulator of BMP/Smad and Akt signalling during early muscle differentiation

artículo científico publicado en 2017

In addition to being a marker for muscle connective tissue, Odd skipped-related 2 (OSR2) is expressed in differentiated muscle cells during chick development

article

Induction of macrophage chemotaxis by aortic extracts of the mgR Marfan mouse model and a GxxPG-containing fibrillin-1 fragment.

artículo científico publicado en 2006

Local retinoic acid signaling directs emergence of the extraocular muscle functional unit

scientific article published on 17 November 2020

Mammalian mitochondrial nitric oxide synthase: characterization of a novel candidate

scientific journal article

Mechanisms of digit formation: Human malformation syndromes tell the story ⬇️

artículo científico publicado el 18 de febrero de 2011

Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia

artículo científico publicado en 2012

Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2.

artículo científico publicado en 2004

Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model

artículo científico publicado en 2015

Multiple roles for neurofibromin in skeletal development and growth

article

Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein

artículo científico publicado en 2010

Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN

scientific journal article

Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome.

artículo científico publicado en 2010

Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures

scientific journal article

Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome

artículo científico publicado en 2006

Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2

artículo científico publicado en 2003

Negative regulation of Wnt signaling mediated by CK1-phosphorylated Dishevelled via Ror2.

artículo científico publicado en 2010

Neurofibromin (Nf1) is required for skeletal muscle development

artículo científico publicado en 2011

Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury

Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development.

artículo científico publicado en 2017

Odd-skipped related genes regulate differentiation of embryonic limb mesenchyme and bone marrow mesenchymal stromal cells.

artículo científico publicado en 2011

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

artículo científico publicado en 2015

Prickle1 is necessary for the caudal migration of murine facial branchiomotor neurons

artículo científico publicado en 2014

Putting Cells into Context

artículo científico publicado en 2017

ROR-Family Receptor Tyrosine Kinases

artículo científico publicado en 2016

Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region

scientific journal article

Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A

Role of Runx genes in chondrocyte differentiation

artículo científico publicado en 2002

Stable and bicistronic expression of two genes in somite- and lateral plate-derived tissues to study chick limb development

artículo científico publicado en 2015

The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling

artículo científico publicado en 2009

The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development.

artículo científico publicado en 2017

The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome

article

The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements

scientific journal article

Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4

artículo científico publicado en 2008

Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion

artículo científico publicado en 2013

Wnt-ligand-dependent interaction of TAK1 (TGF-beta-activated kinase-1) with the receptor tyrosine kinase Ror2 modulates canonical Wnt-signalling

artículo científico publicado en 2008

skNAC and Smyd1 in transcriptional control

artículo científico

Lista de obras de Sigmar Stricker

A Novel Role for the BMP Antagonist Noggin in Sensitizing Cells to Non-canonical Wnt-5a/Ror2/Disheveled Pathway Activation

A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E.

A comparative analysis of Meox1 and Meox2 in the developing somites and limbs of the chick embryo.

A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C.

A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model

A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes

A misplaced lncRNA causes brachydactyly in humans

A molecular pathogenesis for transcription factor associated poly-alanine tract expansions

A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range.

A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution

Abalone (Haliotis tuberculata) hemocyanin type 1 (HtH1) . Organization of the = 400 kDa subunit, and amino acid sequence of its functional units f, g and h

Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders

Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2

An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression

BMP signaling controls muscle mass

Cell autonomous requirement of neurofibromin (Nf1) for postnatal muscle hypertrophic growth and metabolic homeostasis

Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome.

Comparative expression pattern of Odd-skipped related genes Osr1 and Osr2 in chick embryonic development

Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation.

Cooperation of BMP and IHH signaling in interdigital cell fate determination.

Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis

Corrigendum to “Mammalian mitochondrial nitric oxide synthase: Characterization of a novel candidate” [FEBS Lett. 580 (2006) 455-462]

Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion.

Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia.

Editorial: Signaling Pathways in Embryonic Development

Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit

Evolution of a core gene network for skeletogenesis in chordates

Expression of galectin-3 in skeletal tissues is controlled by Runx2.

Expression of type XXIII collagen mRNA and protein

FGF and ROR2 receptor tyrosine kinase signaling in human skeletal development

Faulty initiation of proteoglycan synthesis causes cardiac and joint defects

Genome-wide strategies identify downstream target genes of connective tissue-associated transcription factors

IRS4, a novel modulator of BMP/Smad and Akt signalling during early muscle differentiation

In addition to being a marker for muscle connective tissue, Odd skipped-related 2 (OSR2) is expressed in differentiated muscle cells during chick development

Induction of macrophage chemotaxis by aortic extracts of the mgR Marfan mouse model and a GxxPG-containing fibrillin-1 fragment.

Local retinoic acid signaling directs emergence of the extraocular muscle functional unit

Mammalian mitochondrial nitric oxide synthase: characterization of a novel candidate

Mechanisms of digit formation: Human malformation syndromes tell the story ⬇️

Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia

Modulation of GDF5/BRI-b signalling through interaction with the tyrosine kinase receptor Ror2.

Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model

Multiple roles for neurofibromin in skeletal development and growth

Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein

Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN

Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome.

Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures

Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome

Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2

Negative regulation of Wnt signaling mediated by CK1-phosphorylated Dishevelled via Ror2.

Neurofibromin (Nf1) is required for skeletal muscle development

Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury

Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury

Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development.

Odd-skipped related genes regulate differentiation of embryonic limb mesenchyme and bone marrow mesenchymal stromal cells.

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Prickle1 is necessary for the caudal migration of murine facial branchiomotor neurons

Putting Cells into Context

ROR-Family Receptor Tyrosine Kinases

Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region

Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A

Role of Runx genes in chondrocyte differentiation

Stable and bicistronic expression of two genes in somite- and lateral plate-derived tissues to study chick limb development

The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling

The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development.

The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome

The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements

Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4

Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion

Wnt-ligand-dependent interaction of TAK1 (TGF-beta-activated kinase-1) with the receptor tyrosine kinase Ror2 modulates canonical Wnt-signalling

skNAC and Smyd1 in transcriptional control