A. Burns

F. Collins, S. Libutti, W. Simonds, 2002, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Identification and characterization of JunD missense mutants that lack menin binding

F. Collins, S. Chandrasekharappa, A. Hickman, 2000, Oncogene.

A molecular basis for synexin-driven, calcium-dependent membrane fusion.

E. Rojas, H. Pollard, A. Burns, 1988, The Journal of experimental biology.

The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations.

F. Collins, W. Simonds, L. Weinstein, 2007, The Journal of clinical endocrinology and metabolism.

BRIEF REPORT The Parathyroid/Pituitary Variant of Multiple Endocrine Neoplasia Type 1 Usually Has Causes Other than p27 Kip1 Mutations

F. Collins, W. Simonds, L. Weinstein, 2007 .

Molecular Pathology of the MEN1 Gene

F. Collins, S. Libutti, M. Mullendore, 2004, Annals of the New York Academy of Sciences.

Haplotype analysis defines a minimal interval for the multiple endocrine neoplasia type 1 (MEN1) gene.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Cancer research.

Protein synthesis by the accessory gland of male house cricket,Acheta domesticus

A. Burns, R. Yenofsky, H. E. Potswald, 1975 .

The 32-Kilodalton Subunit of Replication Protein A Interacts with Menin, the Product of the MEN1 Tumor Suppressor Gene

F. Collins, J. Crabtree, S. Chandrasekharappa, 2003, Molecular and Cellular Biology.

Development of structural and functional specializations for export protein synthesis by the accessory gland of the male cricket, Acheta domesticus L. (Orthoptera : Gryllidae)

A. Burns, R. Yenofsky, H. E. Potswald, 1979 .

Mutations of the MEN1 tumor suppressor gene in pituitary tumors.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Cancer research.

Synexin (annexin VII): A cytosolic calcium-binding protein which promotes membrane fusion and forms calcium channels in artificial bilayer and natural membranes

E. Rojas, H. Pollard, A. Burns, 1990, The Journal of Membrane Biology.

Synexin-Driven Membrane Fusion: Molecular Basis for Exocytosis

E. Rojas, H. Pollard, A. Burns, 1990 .

Purification and biochemical assay of synexin and of the homologous calcium-dependent membrane-binding proteins, endonexin II and lipocortin I.

E. Rojas, H. Pollard, D. Schlaepfer, 1989, Methods in cell biology.

Analysis of the translational capacity of the male accessory gland during aging in Acheta domesticus

A. Burns, M. Kaulenas, 1979, Mechanisms of Ageing and Development.

Calcium regulation of membrane fusion during hormone secretion.

H. Pollard, A. Burns, A. Stutzin, 1986, Advances in experimental medicine and biology.

Calcium channel activity of purified human synexin and structure of the human synexin gene.

E. Rojas, H. Pollard, H. Pollard, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Identification of annexins as calcium channels in biological membranes.

E. Rojas, H. Pollard, A. Burns, 1992, Bone and mineral.

Somatic mutation of the MEN1 gene in parathyroid tumours

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Nature Genetics.

Genomic organization and chromosomal localization of the human nucleolin gene.

O. Mcbride, H. Pollard, P. Fleming, 1990, The Journal of biological chemistry.

Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region

B. Roe, M. Boguski, F. Collins, 1997, Human Genetics.

Menin, a tumor suppressor, associates with nonmuscle myosin II-A heavy chain

R. Adelstein, A. Burns, S. Marx, 2003, Oncogene.

Menin Interacts with the AP1 Transcription Factor JunD and Represses JunD-Activated Transcription

F. Collins, M. Erdos, S. Chandrasekharappa, 1999, Cell.

Divergent structure of the human synexin (annexin VII) gene and assignment to chromosome 10.

O. Mcbride, M. Wang, H. Pollard, 1994, Biochemistry.

Genotype/phenotype correlation of multiple endocrine neoplasia type 1 gene mutations in sporadic gastrinomas.

R. Jensen, I. Lubensky, A. Burns, 2000, The Journal of clinical endocrinology and metabolism.

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Human molecular genetics.

Cloning and sequencing of the human nucleolin cDNA

H. Pollard, P. Fleming, A. Burns, 1989, FEBS letters.

Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Human molecular genetics.

Transcription factor JunD, deprived of menin, switches from growth suppressor to growth promoter

F. Collins, J. Weitzman, M. Yaniv, 2003, Proceedings of the National Academy of Sciences of the United States of America.

The tumor suppressor protein menin interacts with NF-κB proteins and inhibits NF-κB-mediated transactivation

F. Collins, K. Bilimoria, S. Chandrasekharappa, 2001, Oncogene.

Multiple endocrine neoplasia type 1: new clinical and basic findings

W. Simonds, M. Skarulis, A. Burns, 2001, Trends in Endocrinology & Metabolism.

Comparative genomic hybridization analysis of human parathyroid tumors.

E. Schröck, T. Ried, C. Heffess, 1998, Cancer genetics and cytogenetics.

Positional cloning of the gene for multiple endocrine neoplasia-type 1.

Y Wang, M S Boguski, B. Roe, 1997, Science.

Menin, the product of the MEN1 gene, is a nuclear protein.

F. Collins, S. Chandrasekharappa, S. Guru, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Menin molecular interactions: insights into normal functions and tumorigenesis.

F. Collins, S. Libutti, B. Oliver, 2005, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Of Mice and MEN1: Insulinomas in a Conditional Mouse Knockout

D. Hanahan, F. Collins, T. Ried, 2003, Molecular and Cellular Biology.

Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysis.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Cancer research.

Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas.

F. Collins, M. Emmert-Buck, A. Vortmeyer, 1997, Cancer research.

Gland Size Is Associated With Changes in Gene Expression Profiles in Sporadic Parathyroid Adenomas

S. Libutti, H. Alexander, H. Alexander, 2004, Annals of Surgical Oncology.

MEN1 gene analysis in sporadic adrenocortical neoplasms.

B. Allolio, A. Burns, A. Spiegel, 1999, The Journal of clinical endocrinology and metabolism.

The gene for multiple endocrine neoplasia type 1: recent findings.

F. Collins, L. Liotta, M. Emmert-Buck, 1999, Bone.

Annexin hypothesis for exocytosis

H. Pollard, A. Burns, 1996 .

Synexin: Molecular Mechanism of Calcium‐Dependent Membrane Fusion and Voltage‐Dependent Calcium‐Channel Activity

H. Guy, H. Pollard, A. Burns, 1991, Annals of the New York Academy of Sciences.

Synexin and Chromaffin Granule Membrane Fusion A Novel “Hydrophobic Bridge” Hypothesis for the Driving and Directing of the Fusion Process a

H. Pollard, A. Burns, E. Rojas, 1987, Annals of the New York Academy of Sciences.

Alternative splicing of human synexin mRNA in brain, cardiac, and skeletal muscle alters the unique N-terminal domain.

H. Pollard, C. Cultraro, A. Burns, 1991, The Journal of biological chemistry.

Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.

F. Collins, L. Liotta, M. Emmert-Buck, 1999, Recent progress in hormone research.

Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 gene

F. Collins, W. Pavan, J. Crabtree, 1999, Mammalian Genome.

Streptomycin: separation of polysomal and non-polysomal messenger ribonucleoproteins.

A. Burns, R. Yenofsky, R. Bosselman, 1977, Biochimica et biophysica acta.

Synexin, a new member of the annexin gene family, is a calcium channel and membrane fusion protein.

E. Rojas, H. Pollard, A. Burns, 1990, Progress in clinical and biological research.

Synexin, Calcium and the Hydrophobic Bridge Hypothesis for Membrane Fusion

E. Rojas, H. Pollard, A. Burns, 1988 .

Calcium channel and membrane fusion activity of synexin and other members of the Annexin gene family.

H. Guy, E. Rojas, H. Pollard, 1992, Biophysical journal.

Synexin (annexin VII) and membrane fusion during the process of exocytotic secretion.

E. Rojas, H. Pollard, A. Burns, 1992, Progress in brain research.

Occurrence of multiple endocrine neoplasia type 1 (MEN-1) gene mutations in patients with zollinger-ellison syndrome (ZES)

R. Jensen, A. Burns, S. Marx, 1998 .

Isolation and characterization of cloned human fetal globin genes.

A. Burns, J. Mears, A. Bank, 1979, Nucleic acids research.

Isolation and characterization of cloned DNA: the delta and beta globin genes in homozygous beta + thalassemia.

A. Markenson, A. Burns, P. Giardina, 1981, Blood.

Parathyroid tumor development involves deregulation of homeobox genes.

F. Collins, S. Libutti, S. Savage, 2008, Endocrine-related cancer.

Properties and Modification of Recombinant Human Synexin (Annexin VII)

H. Pollard, C. Cultraro, A. Burns, 1991, Annals of the New York Academy of Sciences.