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Unraveling the molecular basis for regenerative cellular plasticity

PLoS biology, 2004-08, Vol.2 (8), p.E232-E232

Odelberg, Shannon J

2004

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Dedifferentiation of Mammalian Myotubes Induced by msx1

Cell, 2000-12, Vol.103 (7), p.1099-1109

2000

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Normal newt limb regeneration requires matrix metalloproteinase function

Developmental biology, 2005-03, Vol.279 (1), p.86-98

2005

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Mammalian Myotube Dedifferentiation Induced by Newt Regeneration Extract

Proceedings of the National Academy of Sciences - PNAS, 2001-11, Vol.98 (24), p.13699-13704

2001

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DNA deletion associated with hereditary neuropathy with liability to pressure palsies

Cell, 1993-01, Vol.72 (1), p.143-151

1993

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LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition

Cell, 1996-07, Vol.86 (1), p.59-69

1996

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Human αB-Crystallin Mutation Causes Oxido-Reductive Stress and Protein Aggregation Cardiomyopathy in Mice

Cell, 2007-08, Vol.130 (3), p.427-439

2007

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Template-switching during DNA synthesis by Thermus aquaticus DNA polymerase I

Nucleic acids research, 1995-06, Vol.23 (11), p.2049-2057

1995

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A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12

American journal of human genetics, 1995-02, Vol.56 (2), p.408-415

1995

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Inducing cellular dedifferentiation: a potential method for enhancing endogenous regeneration in mammals

Seminars in cell & developmental biology, 2002-10, Vol.13 (5), p.335-343

Odelberg, Shannon J

2002

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Inducing cellular dedifferentiation: a potential method for enhancing endogenous regeneration in mammals

Seminars in cell & developmental biology, 2002-10, Vol.13 (5), p.335-343

Odelberg, S

2002

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Gene expression signatures in the newt irises during lens regeneration

FEBS letters, 2007-05, Vol.581 (9), p.1865-1870

2007

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Characterization of eight VNTR loci by agarose gel electrophoresis

Genomics (San Diego, Calif.), 1989-11, Vol.5 (4), p.915-924

1989

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An Extended Genetic Linkage Map and an "Index" Map for Human Chromosome 17

Genomics (San Diego, Calif.), 1993, Vol.15 (1), p.38-47

1993

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Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains

The journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1312-1317

1996

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Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains

The journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1312-1317

1996

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Establishing Paternity Using Minisatellite DNA Probes When the Putative Father Is Unavailable for Testing

Journal of forensic sciences, 1988-07, Vol.33 (4), p.921-928

1988

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Tissue inhibitor of metalloproteinase 1 regulates matrix metalloproteinase activity during newt limb regeneration

Developmental dynamics, 2006-03, Vol.235 (3), p.606-616

2006

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Evidence for Proximal to Distal Appendage Amputation Site Effects from Global Gene Expression Correlations Found in Newt Microarrays

2007 IEEE 7th International Symposium on BioInformatics and BioEngineering, 2007, Vol.7, p.131-136

2007

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IEEE_Xplore

Identification of a factor IX point mutation using SSCP analysis and direct sequencing

Nucleic acids research, 1990-09, Vol.18 (18), p.5575-5575

1990

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Heat Map Visualizations Allow Comparison of Multiple Clustering Results and Evaluation of Dataset Quality: Application to Microarray Data

2007 11th International Conference Information Visualization (IV '07), 2007, p.521-526

2007

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IEEE_Xplore

A method for accurate amplification of polymorphic CA-repeat sequences

PCR methods and applications, 1993-08, Vol.3 (1), p.7

1993

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Genetic : abnormalities in sporadic parathyroid adenomas : loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3377-3380

1995

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Generation of variability at VNTR loci in human DNA

EXS (Basel), 1991, Vol.58, p.20

1991

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Genetic abnormalities in sporadic parathyroid adenomas: loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3377-3380

1995

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Unraveling the molecular basis for regenerative cellular plasticity

Dedifferentiation of Mammalian Myotubes Induced by msx1

Normal newt limb regeneration requires matrix metalloproteinase function

Mammalian Myotube Dedifferentiation Induced by Newt Regeneration Extract

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition

Human αB-Crystallin Mutation Causes Oxido-Reductive Stress and Protein Aggregation Cardiomyopathy in Mice

Template-switching during DNA synthesis by Thermus aquaticus DNA polymerase I

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12

Inducing cellular dedifferentiation: a potential method for enhancing endogenous regeneration in mammals

Inducing cellular dedifferentiation: a potential method for enhancing endogenous regeneration in mammals

Gene expression signatures in the newt irises during lens regeneration

Characterization of eight VNTR loci by agarose gel electrophoresis

An Extended Genetic Linkage Map and an "Index" Map for Human Chromosome 17

Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains

Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains

Establishing Paternity Using Minisatellite DNA Probes When the Putative Father Is Unavailable for Testing

Tissue inhibitor of metalloproteinase 1 regulates matrix metalloproteinase activity during newt limb regeneration

Evidence for Proximal to Distal Appendage Amputation Site Effects from Global Gene Expression Correlations Found in Newt Microarrays

Identification of a factor IX point mutation using SSCP analysis and direct sequencing

Heat Map Visualizations Allow Comparison of Multiple Clustering Results and Evaluation of Dataset Quality: Application to Microarray Data

A method for accurate amplification of polymorphic CA-repeat sequences

Genetic : abnormalities in sporadic parathyroid adenomas : loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus

Generation of variability at VNTR loci in human DNA

Genetic abnormalities in sporadic parathyroid adenomas: loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus

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