The triple helix of collagens – an ancient protein structure that enabled animal multicellularity and tissue evolution

P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA

(2017) David M. Hudson et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Lysyl Oxidase-like-2 Cross-links Collagen IV of Glomerular Basement Membrane

(2016) Carolina Añazco et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Extracellular chloride signals collagen IV network assembly during basement membrane formation

(2016) Christopher F. Cummings et al.   JOURNAL OF CELL BIOLOGY

Recessive Mutations in the α3 (VI) Collagen Gene COL6A3 Cause Early-Onset Isolated Dystonia

(2015) Michael Zech et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mammary gland development: cell fate specification, stem cells and the microenvironment

(2015) J. L. Inman et al.   DEVELOPMENT

Hypohalous Acids Contribute to Renal Extracellular Matrix Damage in Experimental Diabetes

(2015) Kyle L. Brown et al.   DIABETES

Mutations in Collagen, Type XVII, Alpha 1 (COL17A1) Cause Epithelial Recurrent Erosion Dystrophy (ERED)

(2015) Frida Jonsson et al.   HUMAN MUTATION

A developmental biologist’s “outside-the-cell” thinking

(2015) David R. Sherwood   JOURNAL OF CELL BIOLOGY

Genomic data do not support comb jellies as the sister group to all other animals

(2015) Davide Pisani et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Error, signal, and the placement of Ctenophora sister to all other animals

(2015) Nathan V. Whelan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Bromine Is an Essential Trace Element for Assembly of Collagen IV Scaffolds in Tissue Development and Architecture

(2014) A. Scott McCall et al.   CELL

Next generation sequencing uncovers a missense mutation in COL4A1 as the cause of familial retinal arteriolar tortuosity

(2014) Juan C. Zenteno et al.   GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

CLAC-P/Collagen Type XXV Is Required for the Intramuscular Innervation of Motoneurons during Neuromuscular Development

(2014) T. Tanaka et al.   JOURNAL OF NEUROSCIENCE

The ctenophore genome and the evolutionary origins of neural systems

(2014) Leonid L. Moroz et al.   NATURE

Remodelling the extracellular matrix in development and disease

(2014) Caroline Bonnans et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

The Genomic and Cellular Foundations of Animal Origins

(2013) Daniel J. Richter et al.   Annual Review of Genetics

ECM-modulated cellular dynamics as a driving force for tissue morphogenesis

(2013) William P Daley et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice

(2013) Yaqun Zou et al.   HUMAN MOLECULAR GENETICS

Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy

(2013) D. Hicks et al.   HUMAN MOLECULAR GENETICS

Posttranslational Modifications in Type I Collagen from Different Tissues Extracted from Wild Type and Prolyl 3-Hydroxylase 1 Null Mice

(2013) Elena Pokidysheva et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Discoidin Domain Receptors: Unique Receptor Tyrosine Kinases in Collagen-mediated Signaling

(2013) Hsueh-Liang Fu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

No evidence for locus heterogeneity in Knobloch syndrome

(2013) Mohammed A Aldahmesh et al.   JOURNAL OF MEDICAL GENETICS

Polyproline-II Helix in Proteins: Structure and Function

(2013) Alexei A. Adzhubei et al.   JOURNAL OF MOLECULAR BIOLOGY

A unique covalent bond in basement membrane is a primordial innovation for tissue evolution

(2013) A. L. Fidler et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The Genome of the Ctenophore Mnemiopsis leidyi and Its Implications for Cell Type Evolution

(2013) J. F. Ryan et al.   SCIENCE

Phenotypic Spectrum ofCOL4A1Mutations: Porencephaly to Schizencephaly

(2012) Yuriko Yoneda et al.   ANNALS OF NEUROLOGY

Discoidin domain receptor tyrosine kinases: new players in cancer progression

(2012) Rajeshwari R. Valiathan et al.   CANCER AND METASTASIS REVIEWS

Transmembrane collagen XVII is a novel component of the glomerular filtration barrier

(2012) Tiina Hurskainen et al.   CELL AND TISSUE RESEARCH

Childhood presentation of COL4A1 mutations

(2012) SIDDHARTH SHAH et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

The evolution of metazoan extracellular matrix

(2012) Richard O. Hynes   JOURNAL OF CELL BIOLOGY

Origin and Evolution of Laminin Gene Family Diversity

(2012) B. Fahey et al.   MOLECULAR BIOLOGY AND EVOLUTION

Peroxidasin forms sulfilimine chemical bonds using hypohalous acids in tissue genesis

(2012) Gautam Bhave et al.   Nature Chemical Biology

De Novo and Inherited Mutations in COL4A2, Encoding the Type IV Collagen α2 Chain Cause Porencephaly

(2011) Yuriko Yoneda et al.   AMERICAN JOURNAL OF HUMAN GENETICS

COL4A2 Mutations Impair COL4A1 and COL4A2 Secretion and Cause Hemorrhagic Stroke

(2011) Marion Jeanne et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Avascular necrosis of the femoral head due to a novel C propeptide mutation in COL2A1

(2011) Peter Kannu et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome

(2011) Stuart Baker et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage

(2011) Yi-Chinn Weng et al.   ANNALS OF NEUROLOGY

Discrepancies in reporting the CAG repeat lengths for Huntington's disease

(2011) Oliver W Quarrell et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A Novel 3-Hydroxyproline (3Hyp)-rich Motif Marks the Triple-helical C Terminus of Tendon Type I Collagen

(2011) David R. Eyre et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Type XII collagen regulates osteoblast polarity and communication during bone formation

(2011) Yayoi Izu et al.   JOURNAL OF CELL BIOLOGY

New perspectives on osteogenesis imperfecta

(2011) Antonella Forlino et al.   Nature Reviews Endocrinology

Collagen XXVII Organises the Pericellular Matrix in the Growth Plate

(2011) Darren A. Plumb et al.   PLoS One

Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene

(2010) Stuart W. Tompson et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel COL4A1 mutations associated with HANAC syndrome: A role for the triple helical CB3[IV] domain

(2010) Emmanuelle Plaisier et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers–Danlos syndrome

(2010) Lee B. Smith et al.   CARDIOVASCULAR RESEARCH

Molecular and structural mapping of collagen fibril interactions

(2010) J. P. R. O. Orgel et al.   CONNECTIVE TISSUE RESEARCH

Drosophila multiplexin (Dmp) modulates motor axon pathfinding accuracy

(2010) Frauke Meyer et al.   DEVELOPMENT GROWTH & DIFFERENTIATION

Loss of procollagen IIA from the anterior mesendoderm disrupts the development of mouse embryonic forebrain

(2010) Alan W.L. Leung et al.   DEVELOPMENTAL DYNAMICS

Origin of animal epithelia: insights from the sponge genome

(2010) Bryony Fahey et al.   EVOLUTION & DEVELOPMENT

Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1

(2010) Allan J. Richards et al.   HUMAN MUTATION

Mapping structural landmarks, ligand binding sites, and missense mutations to the collagen IV heterotrimers predicts major functional domains, novel interactions, and variation in phenotypes in inherited diseases affecting basement membranes

(2010) J. Des Parkin et al.   HUMAN MUTATION

The Fibrillar Collagen Family

(2010) Jean-Yves Exposito et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Identification of the NC1 Domain of α3 Chain as Critical for α3α4α5 Type IV Collagen Network Assembly

(2010) Valerie LeBleu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The Evolution of Extracellular Matrix

(2010) Suat Özbek et al.   MOLECULAR BIOLOGY OF THE CELL

Molecular Architecture of the Goodpasture Autoantigen in Anti-GBM Nephritis

(2010) Vadim Pedchenko et al.   NEW ENGLAND JOURNAL OF MEDICINE

Deletion of the Basement Membrane Heparan Sulfate Proteoglycan Type XVIII Collagen Causes Hypertriglyceridemia in Mice and Humans

(2010) Joseph R. Bishop et al.   PLoS One

Diverse evolutionary paths to cell adhesion

(2010) Monika Abedin et al.   TRENDS IN CELL BIOLOGY

The Collagen Family

(2010) S. Ricard-Blum   Cold Spring Harbor Perspectives in Biology

Basement Membranes: Cell Scaffoldings and Signaling Platforms

(2010) P. D. Yurchenco   Cold Spring Harbor Perspectives in Biology

COL4A1 mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage

(2009) Linda S. de Vries et al.   ANNALS OF NEUROLOGY

Collagen Structure and Stability

(2009) Matthew D. Shoulders et al.   Annual Review of Biochemistry

Epithelia and integration in sponges

(2009) S. P. Leys et al.   INTEGRATIVE AND COMPARATIVE BIOLOGY

Type XIV Collagen Regulates Fibrillogenesis

(2009) Heather L. Ansorge et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The Extracellular Matrix: Not Just Pretty Fibrils

(2009) R. O. Hynes   SCIENCE

A Sulfilimine Bond Identified in Collagen IV

(2009) R. Vanacore et al.   SCIENCE

COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers-Danlos syndrome

(2008) Sofie Symoens et al.   HUMAN MUTATION

Placozoa and the evolution of Metazoa and intrasomatic cell differentiation

(2008) Bernd Schierwater et al.   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

Mammalian collagen IV

(2008) Jamshid Khoshnoodi et al.   MICROSCOPY RESEARCH AND TECHNIQUE

Type IV collagens regulate BMP signalling in Drosophila

(2008) Xiaomeng Wang et al.   NATURE

The genome of the choanoflagellate Monosiga brevicollis and the origin of metazoans

(2008) Nicole King et al.   NATURE

Missense and nonsense mutations in the alternatively-spliced exon 2 ofCOL2A1cause the ocular variant of Stickler syndrome

(2007) Audrey McAlinden et al.   HUMAN MUTATION