Related references
Note: Only part of the references are listed.Interactions between lysyl oxidases and ADAMTS proteins suggest a novel crosstalk between two extracellular matrix families
Rohtem Aviram et al.
MATRIX BIOLOGY (2019)
LOXL3 novel mutation causing a rare form of autosomal recessive Stickler syndrome
Tin K. Chan et al.
CLINICAL GENETICS (2019)
ADAMTS proteins in human disorders
Timothy J. Mead et al.
MATRIX BIOLOGY (2018)
Characteristics, Diagnosis, and Management of Ehlers-Danlos Syndromes A Review
Andrew W. Joseph et al.
JAMA FACIAL PLASTIC SURGERY (2018)
The 2017 International Classification of the Ehlers-Danlos Syndromes
Fransiska Malfait et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2017)
CD and NMR investigation of collagen peptides mimicking a pathological Gly-Ser mutation and a natural interruption in a similar highly charged sequence context
Xiuxia Sun et al.
PROTEIN SCIENCE (2016)
Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant
Akshatha Desai et al.
BMC MUSCULOSKELETAL DISORDERS (2016)
Expanding the clinical and mutational spectrum of the Ehlers-Danlos syndrome, dermatosparaxis type
Tim Van Damme et al.
GENETICS IN MEDICINE (2016)
Consequences of Glycine Mutations in the Fibronectin-binding Sequence of Collagen
Panharith Chhum et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2016)
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans
Vivian S. Lee et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve
Elizabeth M. Bonachea et al.
BMC MEDICAL GENOMICS (2014)
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice
Yaqun Zou et al.
HUMAN MOLECULAR GENETICS (2014)
Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy
Sherry Dadgar et al.
JOURNAL OF CELL BIOLOGY (2014)
Microenvironmental Regulation by Fibrillin-1
Gerhard Sengle et al.
PLOS GENETICS (2012)
Presenting your structures: the CCP4mg molecular-graphics software
S. McNicholas et al.
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY (2011)
Toward an understanding of the protein interaction network of the human liver
Jian Wang et al.
MOLECULAR SYSTEMS BIOLOGY (2011)
Dissection of the internal carotid artery causing Horner syndrome and palsy of cranial nerve XII
Neema Kasravi et al.
CANADIAN MEDICAL ASSOCIATION JOURNAL (2010)
I-TASSER: a unified platform for automated protein structure and function prediction
Ambrish Roy et al.
NATURE PROTOCOLS (2010)
I-TASSER server for protein 3D structure prediction
Yang Zhang
BMC BIOINFORMATICS (2008)
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation
Carine Le Goff et al.
NATURE GENETICS (2008)
Pompe disease diagnosis and management guideline
Priya S. Kishnani et al.
GENETICS IN MEDICINE (2006)
Filamin is essential in actin cytoskeletal assembly mediated by p21-activated kinase 1
RK Vadlamudi et al.
NATURE CELL BIOLOGY (2002)