C. Boyd

K. Csiszȧr, B. Siesjö, P. Li, 2001, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

The gene coding for tropoelastin is represented as a single copy sequence in the haploid sheep genome.

C. Mathew, J. Rosenbloom, J. Davidson, 1987, Collagen and related research.

Increased elastin mRNA levels associated with surgically induced intimal injury.

J. Rosenbloom, R. Pierce, D. C. Miller, 1988, Connective tissue research.

Characterization of a sheep elastin cDNA clone containing translated sequences.

J. Rosenbloom, C. Boyd, Z. Indik, 1984, Biochemical and biophysical research communications.

Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay

A. Munnich, S. Thibodeau, K. Devriendt, 2000, Human Genetics.

Classification of pseudoxanthoma elasticum: report of a consensus conference.

M. Lebwohl, V. McKusick, J. Uitto, 1994, Journal of the American Academy of Dermatology.

Elastin gene mutations in transgenic mice.

D. Riley, L. Sandberg, C. Boyd, 1995, Ciba Foundation symposium.

Characterization of elastin protein and mRNA from salmonid fish (Oncorhynchus kisutch).

R. Mecham, M. Iruela-Arispe, E. Sage, 1989, Comparative biochemistry and physiology. B, Comparative biochemistry.

Changes in vascular extracellular matrix accumulation reflect phenotypic differences between the arterial wall of pigeons resistant and susceptible to the development of spontaneous atherosclerosis.

J. Mackenzie, C. Boyd, S. Y. Yu, 1990, Connective tissue research.

Aortic disease in transgenic mice containing elastin gene mutations

C. Boyd, J. Sechler, 1994 .

Abnormalities in the biosynthesis of type III procollagen in cultured skin fibroblasts from two patients with multiple aneurysms.

J. Ricotta, T. Mariani, J. Mackenzie, 1992, Matrix.

Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndrome.

D. Chitayat, L. Smoot, S. Riazi, 2002, American journal of human genetics.

Ultraviolet radiation increases tropoelastin accumulation by a post-transcriptional mechanism in dermal fibroblasts.

M. Lebwohl, T. Mariani, E. Feinberg, 1995, The Journal of investigative dermatology.

A restriction fragment length polymorphism results in a nonconservative amino acid substitution encoded within the first exon of the human lysyl oxidase gene.

T. Mariani, K. Csiszȧr, C. Boyd, 1993, Genomics.

The size heterogeneity of human lysyl oxidase mRNA is due to alternate polyadenylation site and not alternate exon usage

T. Mariani, K. Csiszȧr, C. Boyd, 2004, Molecular Biology Reports.

Coexpression of the lysyl oxidase‐like gene (LOXL) and the gene encoding type III procollagen in induced liver fibrosis

K. Csiszȧr, Y. Kim, S. Peyrol, 1999, Journal of cellular biochemistry.

Glomerular basement membrane expansion in passive Heymann nephritis. Absence of increased synthesis of type IV collagen, laminin, or fibronectin.

D. Salant, D. Abrahamson, V. Leardkamolkarn, 1991, The American journal of pathology.

Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16.

M. Lebwohl, J. Ott, N. Doggett, 1999, Genomics.

Characterization of the messenger RNA population coding for components of viperid snake venom.

M. Vandenplas, C. Boyd, A. Bester, 1985, Toxicon : official journal of the International Society on Toxinology.

Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcripts

S. Thibodeau, K. Csiszȧr, H. Donis-Keller, 1999, Human Genetics.

A spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticum.

S. Terry, H. Göring, A. De Paepe, 2001, American journal of human genetics.

Identification of heterozygote carriers in families with a recessive form of pseudoxanthoma elasticum (PXE).

O. Le Saux, D. Quaglino, B. Trolli, 1999, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Supravalvular aortic stenosis: genetic and molecular dissection of a complex mutation in the elastin gene

J. Belmont, M. Wallace, E. Davis, 2001, Human Genetics.

cDNA clones coding for the pro-alpha1(IV) chain of human type IV procollagen reveal an unusual homology of amino acid sequences in two halves of the carboxyl-terminal domain.

T. Pihlajaniemi, D. Prockop, R. Lebo, 1985, The Journal of biological chemistry.

Use of an intron polymorphism to localize the tropoelastin gene to mouse chromosome 5 in a region of linkage conservation with human chromosome 7.

C. Boyd, H. Passmore, J. Sechler, 1994, Genomics.

Changes in steady-state levels of mRNAs coding for type IV collagen, laminin and fibronectin following capillary basement membrane thickening in human adult onset diabetes.

J. Mackenzie, C. Boyd, C. Dinerstein, 1990, Connective tissue research.

The tissue distribution of murine Abcc6 (Mrp6) during embryogenesis indicates that the presence of Abcc6 in elastic tissues is not required for elastic fiber assembly

C. Boyd, K. Beck, Ka'ohimanu Dang, 2005, Journal of Molecular Histology.

A to G polymorphism in ELN gene.

J. Rosenbloom, A. Christiano, H. Kuivaniemi, 1991, Nucleic acids research.

In vitro translation of messenger RNA in a rabbit reticulocyte lysate cell-free system.

C. Boyd, L. Olliver, 1996, Methods in molecular biology.

The genes coding for human pro alpha 1(IV) collagen and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13.

J. Mackenzie, M. Condon, S. Toth-Fejel, 1988, American journal of human genetics.

Workshop on pseudoxanthoma elasticum: molecular biology and pathology of the elastic fibers. Jefferson Medical College, Philadelphia, Pennsylvania, June 10, 1992.

M. Lebwohl, J. Uitto, A. Christiano, 1992, The Journal of investigative dermatology.

A quantitative evaluation of SAGE.

J. Stollberg, Z. Urban, C. Boyd, 2000, Genome research.

A tetranucleotide repeat polymorphism within the human elastin gene (ELNi1)

K. Csiszȧr, G. Fekete, Z. Urban, 1997, Clinical genetics.

CHARACTERIZATION OF ELASTIN PROTEIN A N D mRNA FROM SALMONID FISH

R. Mecham, M. Iruela-Arispe, D. Wrenn, 2002 .

International Centennial Meeting on Pseudoxanthoma Elasticum: progress in PXE research.

M. Lebwohl, S. Terry, J. Rosenbloom, 1998, The Journal of investigative dermatology.

Changes in cytoplasmic terminal transferase activities during chick embryo skeletal muscle development

C. Boyd, W. Gevers, A. Bester, 1983, FEBS letters.

Increased procollagen mRNA levels in carbon tetrachloride-induced liver fibrosis in rats.

R. Pierce, J. Mackenzie, R. Greco, 1987, The Journal of biological chemistry.

Increases in Type III Collagen Gene Expression and Protein Synthesis in Patients with Inguinal Hernias

D. W. Friedman, J. Mackenzie, P. Norton, 1993, Annals of surgery.

Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum

S. Terry, K. Csiszȧr, A. De Paepe, 2000, Nature Genetics.

A restriction fragment length polymorphism in the pigeon pro alpha 2(1) collagen gene: lack of an allelic association with an atherogenic phenotype in pigeons genetically susceptible to the development of spontaneous atherosclerosis.

C. Boyd, S. C. Smith, E. C. Smith, 1991, Connective tissue research.

Quantitation of tropoelastin mRNA and assessment of alternative splicing in human skin fibroblasts by reverse transcriptase-polymerase chain reaction.

M. Holzenberger, C. Boyd, S. Deak, 1993, PCR methods and applications.

Analysis of the 3' region of the sheep elastin gene.

J. Davidson, A. Ross, E. Golub, 1985, Archives of biochemistry and biophysics.

Somatic mutations of the lysyl oxidase gene on chromosome 5q23.1 in colorectal tumors

S. Krawetz, S. Fong, K. Csiszȧr, 2002, International journal of cancer.

Sequential Loss of Two Neighboring Exons of the Tropoelastin Gene During Primate Evolution

M. Stoneking, M. Batzer, A. Christiano, 1999, Journal of Molecular Evolution.

Elastic-fiber pathologies: primary defects in assembly-and secondary disorders in transport and delivery.

Z. Urban, C. Boyd, 2000, American journal of human genetics.

7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossover.

A. Munnich, K. Csiszȧr, C. Helms, 1996, American journal of human genetics.

Elements of the rat tropoelastin gene associated with alternative splicing.

R. Pierce, C. Boyd, S. Deak, 1992, Genomics.

Detection of elastin in the human fetal membranes: proposed molecular basis for elasticity.

K. Csiszȧr, H. Kagan, L. Sandberg, 1997, Placenta.

A New Gene with Sequence and Structural Similarity to the Gene Encoding Human Lysyl Oxidase (*)

K. Csiszȧr, C. Boyd, Youngho Kim, 1995, The Journal of Biological Chemistry.

Extensive alternate exon usage at the 5' end of the sheep tropoelastin gene.

A. Christiano, L. Sandberg, C. Boyd, 1995, Matrix biology : journal of the International Society for Matrix Biology.

Heterogeneity of rat tropoelastin mRNA revealed by cDNA cloning.

R. Pierce, C. Stolle, C. Boyd, 1990, Biochemistry.

Functional analysis of the promoter and first intron of the human lysyl oxidase gene

D. Samid, K. Csiszȧr, P. Trackman, 2004, Molecular Biology Reports.

A 30 kb deletion within the elastin gene results in familial supravalvular aortic stenosis.

S. Thibodeau, K. Csiszȧr, D. Driscoll, 1995, Human molecular genetics.

Altered bladder function in transgenic mice expressing rat elastin

K. Csiszȧr, D. Felsen, Z. Urban, 1999, Neurourology and urodynamics.

Conserved and Divergent Sequence and Functional Elements within Collagen Genes

L. Sandell, C. Boyd, 1990 .

A novel fibrotic disorder associated with increased dermal fibroblast proliferation and downregulation of genes of the microfibrillar network

B. Alman, K. Csiszȧr, A. Ordas, 2010, The British journal of dermatology.

Regulation of collagen gene expression in keloids and hypertrophic scars.

D. W. Friedman, J. Mackenzie, P. Norton, 1993, The Journal of surgical research.

The dMRP/CG6214 gene of Drosophila is evolutionarily and functionally related to the human multidrug resistance‐associated protein family

A. Ilias, M. Dean, A. Váradi, 2004, Insect molecular biology.

Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa

S. Terry, D. Viljoen, H. Göring, 2002, Human Genetics.

Multiple Defects in Type III Collagen Synthesis Are Associated with the Pathogenesis of Abdominal Aortic Aneurysms a

H. Kuivaniemi, G. Tromp, C. Stolle, 1996, Annals of the New York Academy of Sciences.

The role of abnormal type III collagen in the development of common aneurysms.

J. Ricotta, T. Mariani, J. Mackenzie, 1992, Journal of vascular surgery.

Isolation and characterization of a 15-kilobase genomic sequence coding for part of the Pro alpha 2 chain of sheep type I collagen.

R. Crystal, M. Schafer, A. Nienhuis, 1980, The Journal of biological chemistry.

Elastin Gene Deletions in Williams Syndrome Patients Result in Altered Deposition of Elastic Fibers in Skin and a Subclinical Dermal Phenotype

M. Lebwohl, K. Csiszȧr, H. Plauchu, 2000, Pediatric dermatology.

A gene‐dosage PCR method for the detection of elastin gene deletions in patients with Williams syndrome

K. Csiszȧr, Z. Urban, C. Boyd, 1998, Clinical genetics.

An intron capture strategy used to identify and map a lysyl oxidase-like gene on chromosome 9 in the mouse.

K. Csiszȧr, Y. Kim, C. Boyd, 1997, Genomics.

A serial analysis of gene expression in sun-damaged human skin.

K. Csiszȧr, Katalin Csiszar, Z. Urban, 2002, The Journal of investigative dermatology.

The effect of viable omentum on early bile leakage and healing of liver lacerations.

R. Pierce, J. Mackenzie, S. Trooskin, 1989, Journal of Trauma.

The Genes Coding for Human Pro o I (IV) Collagen and Pro a2(IV) Collagen Are Both Located at the End of the Long Arm of Chromosome 13

J. Mackenzie, Markku, M. Litt, 2006 .

Large introns in the 3' end of the gene for the pro alpha 1 (IV) chain of human basement membrane collagen.

L. Chow, T. Pihlajaniemi, D. Prockop, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Pressure-induced connective tissue synthesis in pulmonary artery segments is dependent on intact endothelium.

C. Boyd, G. Poiani, D. J. Riley, 1989, The Journal of clinical investigation.

Comparative immunocytochemical localization of lysyl oxidase (LOX) and the lysyl oxidase-like (LOXL) proteins: changes in the expression of LOXL during development and growth of mouse tissues

K. Csiszȧr, K. Fong, C. Boyd, 2004, Journal of Molecular Histology.

(13)C cross-polarization/magic angle spinning NMR studies of alpha-elastin preparations show retention of overall structure and reduction of mobility with a decreased number of cross-links.

L. Sandberg, K. Kumashiro, C. Boyd, 2001, Biopolymers.

Ribosome bound RNA-dependent RNA polymerase: changes in total and specific activity during maturation of avian erythrocytes.

C. Boyd, W. Fitschen, 1975, Biochemical and biophysical research communications.

Elastin morphology in normal and obstructed guinea-pig bladders

C. Boyd, J. Mostwin, O. Karim, 2004, World Journal of Urology.

Persistent Inflammatory Pathways Associated with Early Onset Myocardial Infarction in a Medicated Multiethnic Hawaiian Cohort

K. Csiszȧr, M. Tiirikainen, K. M. Szauter, 2011 .

The Complete Derived Amino Acid Sequence of Human Lysyl Oxidase and Assignment of the Gene to Chromosomes 5

R. Eddy, T. Shows, T. Mariani, 1992 .

Chromosomal localization of the human elastin gene.

J. Rosenbloom, B. Emanuel, L. Cannizzaro, 1985, American journal of human genetics.

Structure of the 3' portion of the bovine elastin gene.

J. Rosenbloom, Z Indik, N Ornstein-Goldstein, 1985, Biochemistry.

Afrikander cattle congenital goiter: size heterogeneity in thyroglobulin mRNA.

C. Boyd, A. Bester, P. V. van Jaarsveld, 1985, Biochemical and biophysical research communications.

Collagen gene expression in the neomatrix of carcinoma of the breast.

I. Wapnir, C. Boyd, G. Chen, 1996, Invasion & metastasis.

Desmoplasia in benign and malignant breast disease is characterized by alterations in level of mRNAs coding for types I and III procollagen.

R. Pierce, J. Mackenzie, R. Greco, 1991, Matrix.

Two new polymorphic markers in the human proα2(1) collagen gene

C. Mathew, C. Boyd, A. Bester, 2004, Human Genetics.

Structural organization of a 17 KB segment of the α2 collagen gene: evaluation by R loop mapping

R. Crystal, M. Schafer, C. Boyd, 1980 .

Structural organization of a 17 KB segment of the alpha 2 collagen gene: evaluation by R loop mapping.

R. Crystal, M. Schafer, C. Boyd, 1980, Nucleic Acids Research.

In vitro translation of messenger RNA in a wheat germ extract cell-free system.

C. Boyd, A. Grobler-Rabie, L. Olliver, 1998, Methods in molecular biology.

Elastin mRNA levels during foetal development of sheep nuchal ligament and lung. Hybridization to complementary and cloned DNA.

M. L. Mason, R. Crystal, S. Shibahara, 1984, The Biochemical journal.

Rat tropoelastin is synthesized from a 3.5-kilobase mRNA.

R. Pierce, D. Riley, C. Boyd, 1988, Journal of Biological Chemistry.

Changes in aortic levels of tropoelastin mRNA following treatment of rats with the antihypertensive drugs captopril and hydralazine.

R. Pierce, J. Mackenzie, C. Boyd, 1991, The Journal of surgical research.

Direct evidence that ribosome bound RNA-dependent RNA polymerase does not play a role in globin messenger RNA replication.

C. Boyd, W. Fitschen, 1977, Nucleic acids research.

Defective splicing of thyroglobulin gene transcripts in the congenital goitre of the Afrikander cattle.

G. Vassart, C. Boyd, V. Pohl, 1985, The EMBO journal.