Citation Impact
Citing Papers
Regulation of Osteogenesis-Angiogenesis Coupling by HIFs and VEGF
2009 StandoutNobel
FGF signaling in skeletal development
1998
Animal models of osteoarthritis
2002
1,25-Dihydroxyvitamin D3 is a negative endocrine regulator of the renin-angiotensin system
2002 Standout
Alternate Exon Usage is a Commonly Used Mechanism for Increasing Coding Diversity Within Genes Coding for Extracellular Matrix Proteins
1993
Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age-onset cataract formation and disruption of the lens
1998 StandoutNobel
Multiple phases of chondrocyte enlargement underlie differences in skeletal proportions
2013 StandoutNature
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 StandoutNature
VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation
1999 Standout
A chromosome 17q de novo paracentric inversion in a patient with campomelic dysplasia; case report and etiologic hypothesis
1991
The Fate of Cartilage Oligomeric Matrix Protein Is Determined by the Cell Type in the Case of a Novel Mutation in Pseudoachondroplasia
1997
Mesenchymal stem cells
1991 Standout
Cell Signaling by Receptor Tyrosine Kinases
2010 Standout
Insights into Extracellular Matrix Functions from Mutant Mouse Models
2000
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome
1998 Standout
Sphingolipids and their metabolism in physiology and disease
2017 Standout
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
1994
Neutral Sphingomyelinase-2 Deficiency Ameliorates Alzheimer's Disease Pathology and Improves Cognition in the 5XFAD Mouse
2016
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
1994 Nature
Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer
2004 Standout
The roles of Fgf4 and Fgf8 in limb bud initiation and outgrowth
2004 StandoutNobel
Inactivation of the FGF-4 Gene in Embryonic Stem Cells Alters the Growth and/or the Survival of Their Early Differentiated Progeny
1997 StandoutNobel
The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos
1995
A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse
2005
Principles of bioactive lipid signalling: lessons from sphingolipids
2008 Standout
Resolving inflammation: dual anti-inflammatory and pro-resolution lipid mediators
2008 Standout
The gene for achondroplasia maps to the telomeric region of chromosome 4p
1994
The biology of VEGF and its receptors
2003 Standout
Alterations in the expression of osteonectin, osteopontin and osteocalcin mRNAs during the development of skeletal tissues in vivo
1994
Characterization of cartilage oligomeric matrix protein (COMP) in human normal and pseudochondroplasia musculoskeletal tissues
1998
The new bone biology: Pathologic, molecular, and clinical correlates
2006
Cartilage proteoglycans: Structure and potential functions
1994
FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease
2002 Standout
FGF signaling inhibits chondrocyte proliferation and regulates bone development through the STAT-1 pathway
1999
Developmental regulation of the growth plate
2003 StandoutNature
WNT signaling in bone homeostasis and disease: from human mutations to treatments
2013 Standout
Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation
1999 Standout
Sox9 is required for cartilage formation
1999 Standout
Fibroblast growth factor signalling: from development to cancer
2010 Standout
SOX9 Binds DNA, Activates Transcription, and Coexpresses with Type II Collagen during Chondrogenesis in the Mouse
1997
Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis
2000 Standout
Avidin as a model for charge driven transport into cartilage and drug delivery for treating early stage post-traumatic osteoarthritis
2013 StandoutNobel
Restrained chondrocyte proliferation and maturation with abnormal growth plate vascularization and ossification in human FGFR-3G380R transgenic mice
2000
The Novel Zinc Finger-Containing Transcription Factor Osterix Is Required for Osteoblast Differentiation and Bone Formation
2002 Standout
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
1995 Standout
Genetic ablation of parathyroid glands reveals another source of parathyroid hormone
2000 Nature
Autophagy is a protective mechanism in normal cartilage, and its aging‐related loss is linked with cell death and osteoarthritis
2010
Common SNPs explain a large proportion of the heritability for human height
2010 Standout
Vascular-specific growth factors and blood vessel formation
2000 StandoutNature
Autophagy and Aging
2011 Standout
The many roles of histone deacetylases in development and physiology: implications for disease and therapy
2008 Standout
Efficient generation of mouse models of human diseases via ABE- and BE-mediated base editing
2018 Standout
The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping
1994
A mutation in the gene encoding the α2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)
1996
From head to toes: the multiple facets of Sox proteins
1999 Standout
Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued by Col2A1-Driven smpd3 Transgene Expression
2007
Mechanism of longitudinal bone growth and its regulation by growth plate chondrocytes
1994
Negative Regulation of Bone Formation by the Transmembrane Wnt Antagonist Kremen-2
2010
New functions for the matrix metalloproteinases in cancer progression
2002 Standout
Cell Signaling by Receptor Tyrosine Kinases
2000 Standout
Structural variations of collagen in normal and pathological tissues: role of electron microscopy
2001
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia.
1996
Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.
1995
RBPjκ-dependent Notch signaling regulates mesenchymal progenitor cell proliferation and differentiation during skeletal development
2010 StandoutNobel
Phenotypic consequences of lung-specific inducible expression of FGF-3
2001 StandoutNobel
Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia
1998
Vascular Endothelial Growth Factor: Basic Science and Clinical Progress
2004 Standout
Ceramide Triggers Budding of Exosome Vesicles into Multivesicular Endosomes
2008 StandoutScience
Multiple roles ofHoxa11andHoxd11in the formation of the mammalian forelimb zeugopod
2003 StandoutNobel
[45] Proteoglycans: Isolation and Characterization
1982
Sox10, a Novel Transcriptional Modulator in Glial Cells
1998 Standout
Dedifferentiated chondrocytes reexpress the differentiated collagen phenotype when cultured in agarose gels
1982 Standout
Enhanced Bone Regeneration Associated With Decreased Apoptosis in Mice With Partial HIF-1α Deficiency
2006 StandoutNobel
Smpd3 Expression in both Chondrocytes and Osteoblasts Is Required for Normal Endochondral Bone Development
2016
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy
2000
The Extended Family of Neutral Sphingomyelinases
2006
The campomelic syndrome: Review, report of 17 cases, and follow‐up on the currently 17‐year‐old boy first reported by Maroteaux et al in 1971
1983
Genetic Dissection of Complex Traits
1994 StandoutScience
Versican gene expression in human articular cartilage and comparison of mRNA splicing variation with aggrecan
1993
MATRIX PROTEOGLYCANS: From Molecular Design to Cellular Function
1998 Standout
Age-related changes in the structure of the proteoglycan subunits from human articular cartilage.
1980
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta.
1993
Regulation of Rate of Cartilage Differentiation by Indian Hedgehog and PTH-Related Protein
1996 StandoutScience
Role of Extracellular Matrix in Adaptation of Tendon and Skeletal Muscle to Mechanical Loading
2004 Standout
Biochemical characteristics and biological significance of the genetically-distinct collagens
1976
The period clock locus of D. melanogaster codes for a proteoglycan
1986 StandoutNobel
Works of V. Stănescu being referenced
Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragility
1991
Familial blomstrand chondrodysplasia with advanced skeletal maturation: Further delineation
1997
Multiple epiphyseal dysplasia, Fairbank type: Morphologic and biochemical study of cartilage
1993
The small proteoglycans of cartilage matrix
1990
Homozygous achondroplasia: Morphologic and biochemical study of cartilage
1990
Variability in the G3 domain content of bovine aggrecan from cartilage extracts and chondrocyte cultures
1992
Non‐collagenous protein screening in the human chondrodysplasias: Link proteins, cartilage oligomeric matrix protein (COMP), and fibromodulin
1994
Immunological Detection of the Egf-Like Domain of the Core Proteins of Large Proteoglycans from Human and Baboon Cartilage
1991
Proteoglycan populations of baboon (Papio papio) articular cartilage. Gel-electrophoretic analysis of fractions obtained by densitygradient centrifugation and by sequential extraction
1977
Early lesions of the articular surface in a strain of mice with very high incidence of spontaneous osteoarthritic-like lesions
1993
Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal
2009
Proteoglycan populations of baboon (Papio papio) cartilages from different anatomical sitesGel electrophoretic analysis of dissociated proteoglycans and of fractions obtained by density gradient centrifugation
1980
Fragilitas ossium: a new autosomal recessive mutation in the mouse
1981
Opsismodysplasia: A new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae
1984
The biochemical defect of pseudoachondroplasia
1982
Metaphyseal anadysplasia: A metaphyseal dysplasia of early onset with radiological regression and benign course
1991
Abnormal Pattern of Segment Long Spacing (SLS) Cartilage Collagen in Diastrophic Dysplasia
1982
Gel Electrophoretic Studies on Proteoglycans and Collagen of Abnormal Human Growth Cartilage: Proteoglycan Abnormalities in Pseudoachondroplasia and in Kniest's Disease
1975
Chemical Studies on the Human Growth Cartilage in Fetuses and Newborns
1973
Pathogenic mechanisms in osteochondrodysplasias.
1984
Articular Degeneration as a Sequela of Osteochondrodysplasias
1985