B. Olsen

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Vascular endothelial growth factor control mechanisms in skeletal growth and repair

Kai Hu, B. Olsen, 2017, Developmental dynamics : an official publication of the American Association of Anatomists.

Laser capture microdissection (LCM) for analysis of gene expression in specific tissues during embryonic epithelial–mesenchymal transformation

E. Hay, A. Nawshad, D. Lagamba, 2004, Developmental dynamics : an official publication of the American Association of Anatomists.

Differential expression of CD146 in tissues and endothelial cells derived from infantile haemangioma and normal human skin

J. Mulliken, J. Bischoff, Ying Yu, 2003, The Journal of pathology.

Skeletal development in vertebrates is initiated by migration of cells from cranial neural crest, somites and lateral plate

N. Fukai, E. Zelzer, Y. Ng, 2002 .

Basement membrane molecule expression attendant to chondrogenesis by nucleus pulposus cells and mesenchymal stem cells

B. Olsen, M. Spector, W. Toh, 2013, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome

Chumpol Ngamphiw, S. Tongsima, A. Tucker, 2022, Clinical genetics.

Snail and Slug Promote Epithelial-Mesenchymal Transition through β-Catenin–T-Cell Factor-4-dependent Expression of Transforming Growth Factor-β3

D. Medici, B. Olsen, 2008 .

Auditory function associated with Col11a1 haploinsufficiency in chondrodysplasia (cho) mice

A. Griffith, K. Kurima, R. Seegmiller, 2003, Hearing Research.

The complete primary structure of two distinct forms of human α(IX) collagen chains

Y. Muragaki, Y. Ninomiya, Tomoatsu Kimura, 1990 .

Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding Sites

Chumpol Ngamphiw, S. Tongsima, P. Kantaputra, 2022, International dental journal.

The role of endothelial‐mesenchymal transition in heterotopic ossification

D. Medici, B. Olsen, 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Cherubism: Best Clinical Practice The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters

M. Papadaki, L. Kaban, M. Levine, 2012 .

Fluocinolone Acetonide Is a Potent Synergistic Factor of TGF‐β3–Associated Chondrogenesis of Bone Marrow–Derived Mesenchymal Stem Cells for Articular Surface Regeneration

M. Takigawa, E. S. Hara, T. Matsumoto, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Altered Growth and Branching Patterns in Synpolydactyly Caused by Mutations in HOXD13

S. Mundlos, Y. Muragaki, J. Upton, 1996, Science.

Primary structure of the long and short splice variants of mouse collagen XII and their tissue‐specific expression during embryonic development

Yefu Li, B. Olsen, Paul S. Oh, 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

Developmental patterns of two α1(IX) collagen mRNA isoforms in mouse

Chia-Yang Liu, B. Olsen, W. Y. Kao, 1993 .

The mouse α1(XII) and human α1(XII)-like collagen genes are localized on mouse chromosome 9 and human chromosome 6

M. Seldin, S. P. Oh, J. Rochelle, 1992 .

Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye

N. Joyce, N. Fukai, G. Wolf, 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Strategies for Directing the Differentiation of Stem Cells Into the Osteogenic Lineage In Vitro

P. Robson, L. Stanton, B. Heng, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Mutations in LRP5 and BMP4 are associated with mesiodens, tooth agenesis, root malformation, and oral exostoses

Chumpol Ngamphiw, S. Tongsima, P. Kantaputra, 2022, Clinical genetics.

Endostatin inhibits VEGF‐induced endothelial cell migration and tumor growth independently of zinc binding

I Que, R. Timpl, Takako Sasaki, 1999, The EMBO journal.

WITHDRAWN; Recent progress in studies of infantile hemangioma

B. Olsen, M. Jinnin, E. Boye, 2010, The Journal of dermatology.

Recent progress in studies of infantile hemangioma

B. Olsen, M. Jinnin, E. Boye, 2010, The Journal of dermatology.

Directed Differentiation of Human Embryonic Stem Cells to Neural Crest Stem Cells, Functional Peripheral Neurons, and Corneal Keratocytes.

Z. Gong, G. Sriram, C. Seneviratne, 2017, Biotechnology journal.

Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney

B. Olsen, N. Fukai, K. Tryggvason, 2003, The EMBO journal.

Developmental Biology of Bone

A. Reginato, B. Olsen, Wenfang Wang, 2001 .

Disproportionate micromelia (Dmm) in mice caused by a mutation in the C‐propeptide coding region of Col2a1

B. Taylor, B. Olsen, C. Teuscher, 1997, Developmental dynamics : an official publication of the American Association of Anatomists.

Role of Cartilage Collagens in Formation of the Skeleton, a

B. Olsen, B. Olsen, 1996, Annals of the New York Academy of Sciences.

Translational Medical Research

O. Ottersen, M. Amiry-Moghaddam, B. Olsen, 2015 .

Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial function

Tiansen Li, B. Pawlyk, B. Olsen, 2004, The EMBO journal.

Growth defect in Grg5 null mice is associated with reduced Ihh signaling in growth plates

You-Gan Wang, Thomas Gridley, You‐Gan Wang, 2002, Developmental dynamics : an official publication of the American Association of Anatomists.

Mouse clavicular development: Analysis of wild‐type and cleidocranial dysplasia mutant mice

S. Mundlos, B. Olsen, L. F. Huang, 1997, Developmental dynamics : an official publication of the American Association of Anatomists.

Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition

B. Olsen, P. LuValle, O. Jacenko, 1993, Nature.

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

B. Olsen, M. Warman, T. Hefferon, 1993, Nature Genetics.

Mutations in the WLS are associated with dental anomalies, torus palatinus, and torus mandibularis.

S. Tongsima, P. Kantaputra, J. R. Ketudat Cairns, 2022, European journal of orthodontics.

Genomic organization and full‐length cDNA sequence of human collagen X

B. Olsen, K. von der Mark, E. Reichenberger, 1992, FEBS letters.

Cloning of human α1(X) collagen DNA and localization of the COL10A1 gene to the q21–q22 region of human chromosome 6

M. Mattei, S. Apte, B. Olsen, 1991, FEBS letters.

The Gene Structure of Tissue Inhibitor of Metalloproteinases (TIMP)-3 and Its Inhibitory Activities Define the Distinct TIMP Gene Family (*)

S. Apte, Bjorn R. Olsen, G. Murphy, 1995, The Journal of Biological Chemistry.

Physiological role of collagen XVIII and endostatin

A. Marneros, B. Olsen, Alexander G. Marneros, 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Secreted cathepsin L generates endostatin from collagen XVIII

H. Ploegh, U. Felbor, R. Bryant, 2000, The EMBO journal.

Structure, function and tissue forms of the C‐terminal globular domain of collagen XVIII containing the angiogenesis inhibitor endostatin

R. Timpl, Takako Sasaki, N. Fukai, 1998, The EMBO journal.

Crystal structure of the angiogenesis inhibitor endostatin at 1.5 Å resolution

R. Timpl, Takako Sasaki, E. Hohenester, 1998, The EMBO journal.

Transformation of Vascular Endothelial Cells into Multipotent Stem-Like Cells: Role of the Activin-Like Kinase 2 Receptor

B. Olsen, D. Medici, B. Olsen, 2012 .

Basic Medical Science

H. B. Benestad, B. Olsen, 2015 .

Knobloch syndrome: Novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin

A. Reymond, S. Antonarakis, S. Deutsch, 2004, Human Mutation.

Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation

S. Tongsima, A. Tucker, P. Kantaputra, 2021, Journal of human genetics.

INVITED EDITORIAL Of Mice and Men: Heritable Skeletal Disorders

M. Warman, O. Jacenko, B. Olsen, 2007 .

Wnt/β-Catenin—A Canonical Tale of Cell-Fate Choice in the Vertebrate Skeleton

B. Olsen, E. Kolpakova, B. Olsen, 2005 .

The highly conserved defender against the death 1 (DAD1) gene maps to human chromosome 14q11–q12 and mouse chromosome 14 and has plant and nematode homologs

M. Seldin, B. Olsen, M. Mattei, 1995, FEBS letters.

Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP‐3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10

M. Seldin, M. Mattei, S. Apte, 1994, Developmental dynamics : an official publication of the American Association of Anatomists.

Craniofacial abnormalities in mice carrying a dominant interference mutation in type X collagen

I. Nishimura, O. Jacenko, B. Olsen, 1997, Developmental Dynamics.

Molecular cloning of rat human type IX collagen cDNA and localization of the α1(IX) gene on the human chromosome 6

B. Olsen, M. Mattei, Y. Ninomiya, 1989 .

The Matrix Metalloproteinase-14 (MMP-14) Gene Is Structurally Distinct from Other MMP Genes and Is Co-expressed with the TIMP-2 Gene during Mouse Embryogenesis*

D. Beier, N. Fukai, S. Apte, 1997, The Journal of Biological Chemistry.

Lack of collagen XVIII/endostatin results in eye abnormalities

N. Fukai, T. Pihlajaniemi, M. Ilves, 2002, The EMBO journal.

The FASEB Journal • Research Communication Endogenous endostatin inhibits choroidal neovascularization

Ivana K. Kim, Joan W. Miller, E. Gragoudas, 2022 .

A new Adamts9 conditional mouse allele identifies its non‐redundant role in interdigital web regression

B. Olsen, S. Apte, Courtney M. Nelson, 2014, Genesis.

Complete Primary Structure of Two Splice Variants of Collagen XII, and Assignment of α1(XII) Collagen (COL12A1), α1(IX) Collagen (COL9A1), and α1(XIX) Collagen (COL19A1) to Human Chromosome 6q12–q13

R. Burgeson, J. Knoll, M. Koch, 1997 .

Matrix Molecules and Their Ligands

B. Olsen, B. Olsen, 2014 .

Fell‐Muir Lecture: Regulatory mechanisms of skeletal and connective tissue development and homeostasis – lessons from studies of human disorders

B. Olsen, Tatiana Y. Besschetnova, Kai Hu, 2016, International journal of experimental pathology.

PDFlib PLOP: PDF Linearization, Optimization, Protection Page inserted by evaluation version

S. Mundlos, P. Selby, B. Olsen, 2006 .

Cleidocranial Dysplasia in Mice

S. Mundlos, B. Olsen, L. F. Huang, 1996, Annals of the New York Academy of Sciences.

Assembly and sequencing of a cDNA covering the entire mouse α1(IX) collagen chain

M. Warman, Y. Muragaki, B. Olsen, 1994 .

WNT10A variant and severe scoliosis?

J. McGrath, P. Kantaputra, B. Olsen, 2022, The Journal of dermatology.

Osteocytes but not osteoblasts directly build mineralized bone structures

Y. Jing, Jian Q. Feng, Yin Xiao, 2021, International journal of biological sciences.

Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth

S. Tongsima, T. Cox, P. Kantaputra, 2023, International journal of molecular sciences.

Shift in Spatial Pattern of Type X Collagen Expression in Embryonic Sterna Undergoing Endochondral Ossification Demonstrated by in Situ Hybridization and Immunohistochemistry

Y. Ninomiya, K. Iyama, R. Trelstad, 1990 .

Type XII collagen. A large multidomain molecule with partial homology to type IX collagen.

B. Olsen, M. E. van der Rest, M. Rest, 1989, The Journal of biological chemistry.

Cartilage type IX collagen-proteoglycan contains a large amino-terminal globular domain encoded by multiple exons.

B. Olsen, G. Vasios, Y. Ninomiya, 1988, The Journal of biological chemistry.

Cloning of the cDNA encoding human tissue inhibitor of metalloproteinases-3 (TIMP-3) and mapping of the TIMP3 gene to chromosome 22.

B. Olsen, M. Mattei, S. Apte, 1994, Genomics.

Collagen XII Mutation Disrupts Matrix Structure of Periodontal Ligament and Skin

C. Sukotjo, N. Karimbux, I. Nishimura, 2000 .

A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrix

D. Rimoin, P. Roughley, B. Olsen, 1994, Human Genetics.

Mouse Col18a1 is expressed in a tissue-specific manner as three alternative variants and is localized in basement membrane zones.

T. Quertermous, B. Olsen, Y. Muragaki, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Tissue-specific forms of type IX collagen-proteoglycan arise from the use of two widely separated promoters.

B. Olsen, Y. Muragaki, I. Nishimura, 1989, The Journal of biological chemistry.