List of Faculty Publications

Below is a list of Faculty publications imported from PubMed or manually added. By default, publications are sorted by year with titles displayed in ascending alphabetical order.
Shortcuts: Wühr, Martin | Wingreen, Ned | Wieschaus, Eric | Troyanskaya, Olga | Tilghman, Shirley | Storey, John | Singh, Mona | Shvartsman, Stanislav | Shaevitz, Joshua | Rabinowitz, Joshua | Murphy, Coleen | Levine, Michael {Levine, Michael S.} | Gregor, Thomas | Botstein, David | Bialek, William | Ayroles, Julien | Andolfatto, Peter | Akey, Joshua

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Mice
J. M. Rossi, Burke, D. T., Leung, J. C., Koos, D. S., Chen, H., and Tilghman, S. M., Genomic analysis using a yeast artificial chromosome library with mouse DNA inserts., Proc Natl Acad Sci U S A, vol. 89, no. 6, pp. 2456-60, 1992.
J. V. Schmidt, Levorse, J. M., and Tilghman, S. M., Enhancer competition between H19 and Igf2 does not mediate their imprinting., Proc Natl Acad Sci U S A, vol. 96, no. 17, pp. 9733-8, 1999.
C. D. van Raamsdonk and Tilghman, S. M., Optimizing the detection of nascent transcripts by RNA fluorescence in situ hybridization., Nucleic Acids Res, vol. 29, no. 8, pp. E42-2, 2001.
M. S. Bartolomei, Zemel, S., and Tilghman, S. M., Parental imprinting of the mouse H19 gene., Nature, vol. 351, no. 6322, pp. 153-5, 1991.
W. J. Pavan and Tilghman, S. M., Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes., Proc Natl Acad Sci U S A, vol. 91, no. 15, pp. 7159-63, 1994.
C. D. van Raamsdonk and Tilghman, S. M., Dosage requirement and allelic expression of PAX6 during lens placode formation., Development, vol. 127, no. 24, pp. 5439-48, 2000.
C. I. Brannan, Dees, E. C., Ingram, R. S., and Tilghman, S. M., The product of the H19 gene may function as an RNA., Mol Cell Biol, vol. 10, no. 1, pp. 28-36, 1990.
J. Vacher, Camper, S. A., Krumlauf, R., Compton, R. S., and Tilghman, S. M., raf regulates the postnatal repression of the mouse alpha-fetoprotein gene at the posttranscriptional level., Mol Cell Biol, vol. 12, no. 2, pp. 856-64, 1992.
D. L. Metallinos, Oppenheimer, A. J., Rinchik, E. M., Russell, L. B., Dietrich, W., and Tilghman, S. M., Fine structure mapping and deletion analysis of the murine piebald locus., Genetics, vol. 136, no. 1, pp. 217-23, 1994.
M. K. Shin, Russell, L. B., and Tilghman, S. M., Molecular characterization of four induced alleles at the Ednrb locus., Proc Natl Acad Sci U S A, vol. 94, no. 24, pp. 13105-10, 1997.
B. K. Jones, Levorse, J., and Tilghman, S. M., Deletion of a nuclease-sensitive region between the Igf2 and H19 genes leads to Igf2 misregulation and increased adiposity., Hum Mol Genet, vol. 10, no. 8, pp. 807-14, 2001.
T. Caspary, Cleary, M. A., Baker, C. C., Guan, X. J., and Tilghman, S. M., Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster., Mol Cell Biol, vol. 18, no. 6, pp. 3466-74, 1998.
P. A. Leighton, Ingram, R. S., Eggenschwiler, J., Efstratiadis, A., and Tilghman, S. M., Disruption of imprinting caused by deletion of the H19 gene region in mice., Nature, vol. 375, no. 6526, pp. 34-9, 1995.
A. L. Webber, Ingram, R. S., Levorse, J. M., and Tilghman, S. M., Location of enhancers is essential for the imprinting of H19 and Igf2 genes., Nature, vol. 391, no. 6668, pp. 711-5, 1998.
J. A. Emerson, Vacher, J., Cirillo, L. A., Tilghman, S. M., and Tyner, A. L., The zonal expression of alpha-fetoprotein transgenes in the livers of adult mice., Dev Dyn, vol. 195, no. 1, pp. 55-66, 1992.
Mice, Inbred C57BL
J. M. Rossi, Burke, D. T., Leung, J. C., Koos, D. S., Chen, H., and Tilghman, S. M., Genomic analysis using a yeast artificial chromosome library with mouse DNA inserts., Proc Natl Acad Sci U S A, vol. 89, no. 6, pp. 2456-60, 1992.
W. J. Pavan and Tilghman, S. M., Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes., Proc Natl Acad Sci U S A, vol. 91, no. 15, pp. 7159-63, 1994.
M. K. Shin, Russell, L. B., and Tilghman, S. M., Molecular characterization of four induced alleles at the Ednrb locus., Proc Natl Acad Sci U S A, vol. 94, no. 24, pp. 13105-10, 1997.
A. L. Webber, Ingram, R. S., Levorse, J. M., and Tilghman, S. M., Location of enhancers is essential for the imprinting of H19 and Igf2 genes., Nature, vol. 391, no. 6668, pp. 711-5, 1998.
L. J. Kurihara, Kikuchi, T., Wada, K., and Tilghman, S. M., Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia., Hum Mol Genet, vol. 10, no. 18, pp. 1963-70, 2001.
P. A. Leighton, Ingram, R. S., Eggenschwiler, J., Efstratiadis, A., and Tilghman, S. M., Disruption of imprinting caused by deletion of the H19 gene region in mice., Nature, vol. 375, no. 6526, pp. 34-9, 1995.
S. M. Tilghman, Bartolomei, M. S., Webber, A. L., Brunkow, M. E., Saam, J., Leighton, P. A., Pfeifer, K., and Zemel, S., Parental imprinting of the H19 and Igf2 genes in the mouse., Cold Spring Harb Symp Quant Biol, vol. 58, pp. 287-95, 1993.
T. Caspary, Cleary, M. A., Perlman, E. J., Zhang, P., Elledge, S. J., and Tilghman, S. M., Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome., Genes Dev, vol. 13, no. 23, pp. 3115-24, 1999.
A. T. Hark and Tilghman, S. M., Chromatin conformation of the H19 epigenetic mark., Hum Mol Genet, vol. 7, no. 12, pp. 1979-85, 1998.
M. E. Brunkow and Tilghman, S. M., Ectopic expression of the H19 gene in mice causes prenatal lethality., Genes Dev, vol. 5, no. 6, pp. 1092-101, 1991.
K. Pfeifer, Leighton, P. A., and Tilghman, S. M., The structural H19 gene is required for transgene imprinting., Proc Natl Acad Sci U S A, vol. 93, no. 24, pp. 13876-83, 1996.
M. A. Cleary, van Raamsdonk, C. D., Levorse, J., Zheng, B., Bradley, A., and Tilghman, S. M., Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice., Nat Genet, vol. 29, no. 1, pp. 78-82, 2001.
D. T. Burke, Rossi, J. M., Leung, J., Koos, D. S., and Tilghman, S. M., A mouse genomic library of yeast artificial chromosome clones., Mamm Genome, vol. 1, no. 1, p. 65, 1991.
X. J. Guan, Arhin, G., Leung, J., and Tilghman, S. M., Linkage between vitamin D-binding protein and alpha-fetoprotein in the mouse., Mamm Genome, vol. 7, no. 2, pp. 103-6, 1996.
M. S. Bartolomei, Webber, A. L., Brunkow, M. E., and Tilghman, S. M., Epigenetic mechanisms underlying the imprinting of the mouse H19 gene., Genes Dev, vol. 7, no. 9, pp. 1663-73, 1993.
M. K. Shin, Levorse, J. M., Ingram, R. S., and Tilghman, S. M., The temporal requirement for endothelin receptor-B signalling during neural crest development., Nature, vol. 402, no. 6761, pp. 496-501, 1999.
B. K. Jones, Levorse, J., and Tilghman, S. M., Deletion of a nuclease-sensitive region between the Igf2 and H19 genes leads to Igf2 misregulation and increased adiposity., Hum Mol Genet, vol. 10, no. 8, pp. 807-14, 2001.
Mice, Mutant Strains
T. P. O'Brien, Metallinos, D. L., Chen, H., Shin, M. K., and Tilghman, S. M., Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex., Genetics, vol. 143, no. 1, pp. 447-61, 1996.
C. D. van Raamsdonk and Tilghman, S. M., Dosage requirement and allelic expression of PAX6 during lens placode formation., Development, vol. 127, no. 24, pp. 5439-48, 2000.
L. J. Kurihara, Kikuchi, T., Wada, K., and Tilghman, S. M., Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia., Hum Mol Genet, vol. 10, no. 18, pp. 1963-70, 2001.
D. L. Metallinos, Oppenheimer, A. J., Rinchik, E. M., Russell, L. B., Dietrich, W., and Tilghman, S. M., Fine structure mapping and deletion analysis of the murine piebald locus., Genetics, vol. 136, no. 1, pp. 217-23, 1994.
J. M. Rossi, Chen, H., and Tilghman, S. M., Genetic map of the fused locus on mouse chromosome 17., Genomics, vol. 23, no. 1, pp. 178-84, 1994.
T. Caspary, Cleary, M. A., Perlman, E. J., Zhang, P., Elledge, S. J., and Tilghman, S. M., Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome., Genes Dev, vol. 13, no. 23, pp. 3115-24, 1999.
W. J. Pavan, Mac, S., Cheng, M., and Tilghman, S. M., Quantitative trait loci that modify the severity of spotting in piebald mice., Genome Res, vol. 5, no. 1, pp. 29-41, 1995.
Mice, Transgenic
J. A. Emerson, Vacher, J., Cirillo, L. A., Tilghman, S. M., and Tyner, A. L., The zonal expression of alpha-fetoprotein transgenes in the livers of adult mice., Dev Dyn, vol. 195, no. 1, pp. 55-66, 1992.
S. M. Tilghman, Bartolomei, M. S., Webber, A. L., Brunkow, M. E., Saam, J., Leighton, P. A., Pfeifer, K., and Zemel, S., Parental imprinting of the H19 and Igf2 genes in the mouse., Cold Spring Harb Symp Quant Biol, vol. 58, pp. 287-95, 1993.
A. L. Tyner, Godbout, R., Compton, R. S., and Tilghman, S. M., The ontogeny of alpha-fetoprotein gene expression in the mouse gastrointestinal tract., J Cell Biol, vol. 110, no. 4, pp. 915-27, 1990.
M. E. Brunkow and Tilghman, S. M., Ectopic expression of the H19 gene in mice causes prenatal lethality., Genes Dev, vol. 5, no. 6, pp. 1092-101, 1991.
J. H. Millonig, Emerson, J. A., Levorse, J. M., and Tilghman, S. M., Molecular analysis of the distal enhancer of the mouse alpha-fetoprotein gene., Mol Cell Biol, vol. 15, no. 7, pp. 3848-56, 1995.
S. A. Camper and Tilghman, S. M., Postnatal repression of the alpha-fetoprotein gene is enhancer independent., Genes Dev, vol. 3, no. 4, pp. 537-46, 1989.
K. Pfeifer, Leighton, P. A., and Tilghman, S. M., The structural H19 gene is required for transgene imprinting., Proc Natl Acad Sci U S A, vol. 93, no. 24, pp. 13876-83, 1996.
A. T. Hark, Schoenherr, C. J., Katz, D. J., Ingram, R. S., Levorse, J. M., and Tilghman, S. M., CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus., Nature, vol. 405, no. 6785, pp. 486-9, 2000.
Molecular Sequence Data
P. A. Leighton, Ingram, R. S., Eggenschwiler, J., Efstratiadis, A., and Tilghman, S. M., Disruption of imprinting caused by deletion of the H19 gene region in mice., Nature, vol. 375, no. 6526, pp. 34-9, 1995.
J. A. Emerson, Vacher, J., Cirillo, L. A., Tilghman, S. M., and Tyner, A. L., The zonal expression of alpha-fetoprotein transgenes in the livers of adult mice., Dev Dyn, vol. 195, no. 1, pp. 55-66, 1992.
P. B. Vrana, Guan, X. J., Ingram, R. S., and Tilghman, S. M., Genomic imprinting is disrupted in interspecific Peromyscus hybrids., Nat Genet, vol. 20, no. 4, pp. 362-5, 1998.
K. Pfeifer and Tilghman, S. M., Allele-specific gene expression in mammals: the curious case of the imprinted RNAs., Genes Dev, vol. 8, no. 16, pp. 1867-74, 1994.
P. A. Leighton, Saam, J. R., Ingram, R. S., Stewart, C. L., and Tilghman, S. M., An enhancer deletion affects both H19 and Igf2 expression., Genes Dev, vol. 9, no. 17, pp. 2079-89, 1995.
H. Yoo-Warren, Pachnis, V., Ingram, R. S., and Tilghman, S. M., Two regulatory domains flank the mouse H19 gene., Mol Cell Biol, vol. 8, no. 11, pp. 4707-15, 1988.
R. Godbout, Ingram, R. S., and Tilghman, S. M., Fine-structure mapping of the three mouse alpha-fetoprotein gene enhancers., Mol Cell Biol, vol. 8, no. 3, pp. 1169-78, 1988.
J. M. Rossi, Chen, H., and Tilghman, S. M., Genetic map of the fused locus on mouse chromosome 17., Genomics, vol. 23, no. 1, pp. 178-84, 1994.
J. H. Millonig, Emerson, J. A., Levorse, J. M., and Tilghman, S. M., Molecular analysis of the distal enhancer of the mouse alpha-fetoprotein gene., Mol Cell Biol, vol. 15, no. 7, pp. 3848-56, 1995.
X. J. Guan, Arhin, G., Leung, J., and Tilghman, S. M., Linkage between vitamin D-binding protein and alpha-fetoprotein in the mouse., Mamm Genome, vol. 7, no. 2, pp. 103-6, 1996.
T. P. O'Brien, Metallinos, D. L., Chen, H., Shin, M. K., and Tilghman, S. M., Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex., Genetics, vol. 143, no. 1, pp. 447-61, 1996.
P. B. Vrana, Matteson, P. G., Schmidt, J. V., Ingram, R. S., Joyce, A., Prince, K. L., Dewey, M. J., and Tilghman, S. M., Genomic imprinting of a placental lactogen gene in Peromyscus., Dev Genes Evol, vol. 211, no. 11, pp. 523-32, 2001.
L. J. Kurihara, Semenova, E., Levorse, J. M., and Tilghman, S. M., Expression and functional analysis of Uch-L3 during mouse development., Mol Cell Biol, vol. 20, no. 7, pp. 2498-504, 2000.
J. M. Rossi, Burke, D. T., Leung, J. C., Koos, D. S., Chen, H., and Tilghman, S. M., Genomic analysis using a yeast artificial chromosome library with mouse DNA inserts., Proc Natl Acad Sci U S A, vol. 89, no. 6, pp. 2456-60, 1992.
C. I. Brannan, Dees, E. C., Ingram, R. S., and Tilghman, S. M., The product of the H19 gene may function as an RNA., Mol Cell Biol, vol. 10, no. 1, pp. 28-36, 1990.
J. Vacher, Camper, S. A., Krumlauf, R., Compton, R. S., and Tilghman, S. M., raf regulates the postnatal repression of the mouse alpha-fetoprotein gene at the posttranscriptional level., Mol Cell Biol, vol. 12, no. 2, pp. 856-64, 1992.
D. L. Metallinos, Oppenheimer, A. J., Rinchik, E. M., Russell, L. B., Dietrich, W., and Tilghman, S. M., Fine structure mapping and deletion analysis of the murine piebald locus., Genetics, vol. 136, no. 1, pp. 217-23, 1994.
Mothers
S. M. Tilghman, Parental imprinting in the mouse., Harvey Lect, vol. 87, pp. 69-84, 1991.
Muscle Proteins
A. T. Hark, Schoenherr, C. J., Katz, D. J., Ingram, R. S., Levorse, J. M., and Tilghman, S. M., CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus., Nature, vol. 405, no. 6785, pp. 486-9, 2000.
J. V. Schmidt, Levorse, J. M., and Tilghman, S. M., Enhancer competition between H19 and Igf2 does not mediate their imprinting., Proc Natl Acad Sci U S A, vol. 96, no. 17, pp. 9733-8, 1999.
A. L. Webber, Ingram, R. S., Levorse, J. M., and Tilghman, S. M., Location of enhancers is essential for the imprinting of H19 and Igf2 genes., Nature, vol. 391, no. 6668, pp. 711-5, 1998.
T. Caspary, Cleary, M. A., Baker, C. C., Guan, X. J., and Tilghman, S. M., Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster., Mol Cell Biol, vol. 18, no. 6, pp. 3466-74, 1998.
B. K. Jones, Levorse, J. M., and Tilghman, S. M., Igf2 imprinting does not require its own DNA methylation or H19 RNA., Genes Dev, vol. 12, no. 14, pp. 2200-7, 1998.
P. A. Leighton, Saam, J. R., Ingram, R. S., Stewart, C. L., and Tilghman, S. M., An enhancer deletion affects both H19 and Igf2 expression., Genes Dev, vol. 9, no. 17, pp. 2079-89, 1995.
T. Caspary, Cleary, M. A., Perlman, E. J., Zhang, P., Elledge, S. J., and Tilghman, S. M., Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome., Genes Dev, vol. 13, no. 23, pp. 3115-24, 1999.
A. T. Hark and Tilghman, S. M., Chromatin conformation of the H19 epigenetic mark., Hum Mol Genet, vol. 7, no. 12, pp. 1979-85, 1998.
K. Pfeifer, Leighton, P. A., and Tilghman, S. M., The structural H19 gene is required for transgene imprinting., Proc Natl Acad Sci U S A, vol. 93, no. 24, pp. 13876-83, 1996.
A. L. Webber and Tilghman, S. M., The absence of enhancer competition between Igf2 and H19 following transfer into differentiated cells., Mol Cell Biol, vol. 18, no. 4, pp. 1903-10, 1998.
Mutation
S. M. Tilghman, DNA methylation: a phoenix rises., Proc Natl Acad Sci U S A, vol. 90, no. 19, pp. 8761-2, 1993.
R. Godbout, Ingram, R. S., and Tilghman, S. M., Fine-structure mapping of the three mouse alpha-fetoprotein gene enhancers., Mol Cell Biol, vol. 8, no. 3, pp. 1169-78, 1988.
L. J. Kurihara, Semenova, E., Levorse, J. M., and Tilghman, S. M., Expression and functional analysis of Uch-L3 during mouse development., Mol Cell Biol, vol. 20, no. 7, pp. 2498-504, 2000.
T. J. Vasicek, Zeng, L., Guan, X. J., Zhang, T., Costantini, F., and Tilghman, S. M., Two dominant mutations in the mouse fused gene are the result of transposon insertions., Genetics, vol. 147, no. 2, pp. 777-86, 1997.
D. L. Metallinos, Oppenheimer, A. J., Rinchik, E. M., Russell, L. B., Dietrich, W., and Tilghman, S. M., Fine structure mapping and deletion analysis of the murine piebald locus., Genetics, vol. 136, no. 1, pp. 217-23, 1994.
C. D. van Raamsdonk and Tilghman, S. M., Dosage requirement and allelic expression of PAX6 during lens placode formation., Development, vol. 127, no. 24, pp. 5439-48, 2000.
W. J. Pavan and Tilghman, S. M., Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes., Proc Natl Acad Sci U S A, vol. 91, no. 15, pp. 7159-63, 1994.
L. J. Kurihara, Kikuchi, T., Wada, K., and Tilghman, S. M., Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia., Hum Mol Genet, vol. 10, no. 18, pp. 1963-70, 2001.
Paternity
S. M. Tilghman, Parental imprinting in the mouse., Harvey Lect, vol. 87, pp. 69-84, 1991.
Point Mutation
M. K. Shin, Russell, L. B., and Tilghman, S. M., Molecular characterization of four induced alleles at the Ednrb locus., Proc Natl Acad Sci U S A, vol. 94, no. 24, pp. 13105-10, 1997.
S. M. Tilghman, DNA methylation: a phoenix rises., Proc Natl Acad Sci U S A, vol. 90, no. 19, pp. 8761-2, 1993.
Protein Biosynthesis
C. I. Brannan, Dees, E. C., Ingram, R. S., and Tilghman, S. M., The product of the H19 gene may function as an RNA., Mol Cell Biol, vol. 10, no. 1, pp. 28-36, 1990.
Receptor, IGF Type 2
S. M. Tilghman, DNA methylation: a phoenix rises., Proc Natl Acad Sci U S A, vol. 90, no. 19, pp. 8761-2, 1993.
P. A. Leighton, Saam, J. R., Ingram, R. S., and Tilghman, S. M., Genomic imprinting in mice: its function and mechanism., Biol Reprod, vol. 54, no. 2, pp. 273-8, 1996.

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