Marie Elise Mangelsdorf

Aristaless-related homeobox gene, the gene responsible for west syndrome and related disorders, is a groucho/transducin-like enhancer of split dependent transcriptional repressor (2007)

McKenzie, Olivia L. D., Ponte, I., Mangelsdorf, Marie Elise, Finnis, Merran, Colasante, G., Shoubridge, C. A., ...

Copyright © 2007 IBRO Published by Elsevier Ltd.

Aristaless-related homeobox gene, the gene responsible for west syndrome and related disorders, is a groucho/transducin-like enhancer of split dependent transcriptional repressor (2007)

McKenzie, Olivia L. D., Ponte, I., Mangelsdorf, Marie Elise, Finnis, Merran, Colasante, G., Shoubridge, C. A., ...

Copyright © 2007 IBRO Published by Elsevier Ltd.

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene (2005)

Stepp, Monica L., Cason, A. Lauren, Finnis, Merran, Mangelsdorf, Marie Elise, Holinski-Feder, Elke, Macgregor, David, ...

© 2005 Stepp et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),...

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene (2005)

Stepp, Monica L., Cason, A. Lauren, Finnis, Merran, Mangelsdorf, Marie Elise, Holinski-Feder, Elke, Macgregor, David, ...

© 2005 Stepp et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),...

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation (2004)

Tarpey, P., Parnau, J., Blow, M., Woffendin, H., Bignell, G., Cox, C., ...

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation (2004)

Tarpey, P., Parnau, J., Blow, M., Woffendin, H., Bignell, G., Cox, C., ...

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein (2004)

Sarafidou, T., Kahl, C., Martinez-Garay, I., Mangelsdorf, Marie Elise, Gesk, S., Baker, Elizabeth Gay, ...

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation (2004)

Tarpey, P., Parnau, J., Blow, M., Woffendin, H., Bignell, G., Cox, C., ...

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein (2004)

Sarafidou, T., Kahl, C., Martinez-Garay, I., Mangelsdorf, Marie Elise, Gesk, S., Baker, Elizabeth Gay, ...

Identification of novel genes for x-linked mental retardation / by Marie Mangelsdorf. (2003)

Mangelsdorf, Marie Elise

"May 2003"

Identification of novel genes for x-linked mental retardation / by Marie Mangelsdorf. (2003)

Mangelsdorf, Marie Elise

"May 2003"

Identification of novel genes for x-linked mental retardation / by Marie Mangelsdorf. (2003)

Mangelsdorf, Marie Elise

"May 2003"

Identification of novel genes for x-linked mental retardation / by Marie Mangelsdorf. (2003)

Mangelsdorf, Marie Elise

"May 2003"

Identification of novel genes for x-linked mental retardation / by Marie Mangelsdorf. (2003)

Mangelsdorf, Marie Elise

"May 2003"

Identification of novel genes for x-linked mental retardation (2003)

Mangelsdorf, Marie Elise.

"May 2003" Bibliography: leaves 187-213.

Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation (2002)

Turner, G., Partington, M., Kerr, B., Mangelsdorf, Marie Elise, Gecz, J.

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX (2002)

Stromme, P., Mangelsdorf, Marie Elise, Scheffer, I. E., Gecz, J.

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy (2002)

Stromme, P., Mangelsdorf, Marie Elise, Shaw, M. A., Lower, K. M., Lewis, S. M., Bruyere, H., ...

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy (2002)

Stromme, P., Mangelsdorf, Marie Elise, Shaw, M. A., Lower, K. M., Lewis, S. M., Bruyere, H., ...

Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation (2002)

Turner, G., Partington, M., Kerr, B., Mangelsdorf, Marie Elise, Gecz, J.

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX (2002)

Stromme, P., Mangelsdorf, Marie Elise, Scheffer, I. E., Gecz, J.

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy (2002)

Stromme, P., Mangelsdorf, Marie Elise, Shaw, M. A., Lower, K. M., Lewis, S. M., Bruyere, H., ...

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells (2000)

Ried, Karin, Finnis, M. L., Hobson, L., Mangelsdorf, Marie Elise, Dayan, S., Nancarrow, J., ...

Fluorescence in situ hybridization of a tile path of DNA subclones has previously enabled the cyto­genetic definition of the minimal DNA sequence which spans the FRA16D common chromosomal fragile...

Chromosomal fragile site FRA16D and DNA instability in cancer (2000)

Mangelsdorf, Marie Elise, Ried, Karin, Woollatt, E., Dayan, S., Eyre, H., Finnis, M. L., ...

It has been proposed that common aphidicolin-inducible fragile sites, in general, predispose to specific chromosomal breakage associated with deletion, amplification, and/or translocation in certain...

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells (2000)

Ried, Karin, Finnis, M. L., Hobson, L., Mangelsdorf, Marie Elise, Dayan, S., Nancarrow, J., ...

Fluorescence in situ hybridization of a tile path of DNA subclones has previously enabled the cyto­genetic definition of the minimal DNA sequence which spans the FRA16D common chromosomal fragile...

Chromosomal fragile site FRA16D and DNA instability in cancer (2000)

Mangelsdorf, Marie Elise, Ried, Karin, Woollatt, E., Dayan, S., Eyre, H., Finnis, M. L., ...

It has been proposed that common aphidicolin-inducible fragile sites, in general, predispose to specific chromosomal breakage associated with deletion, amplification, and/or translocation in certain...

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis (1998)

Hewett, D. R., Handt, O., Hobson, L., Mangelsdorf, Marie Elise, Eyre, H. J., Baker, E., ...

A common mechanism for chromosomal fragile site genesis is not yet apparent. Folate-sensitive fragile sites are expanded p(CCG)n repeats that arise from longer normal alleles. Distamycin A or...

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis (1998)

Hewett, D. R., Handt, O., Hobson, L., Mangelsdorf, Marie Elise, Eyre, H. J., Baker, E., ...

A common mechanism for chromosomal fragile site genesis is not yet apparent. Folate-sensitive fragile sites are expanded p(CCG)n repeats that arise from longer normal alleles. Distamycin A or...

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat (1997)

Yu, S., Mangelsdorf, Marie Elise, Hewett, D., Hobson, L., Baker, E., Eyre, H. J., ...

Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2 (1997)

Horwitz, M., Benson, K. F., Li, F-Q., Wolff, J., Leppert, M. F., Hobson, L., ...

Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever (1997)

Aksentijevich, I., Centola, M., Deng, Z., Sood, R., Balow, J. E., ...

Human chromosomal fragile site FRA16B is an amplified AT-Rich minisatellite repeat (1997)

Yu, S., Mangelsdorf, Marie Elise, Hewett, D., Hobson, L., Baker, E., Eyre, H. J., ...

Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the Familial Mediterranean Fever Locus (MEFV) on chromosome 16p13.3 (1997)

Sood, R., Blake, T., Aksentijevich, I., Wood, G., Chen, X., Gardner, D., ...

A high-resolution genetic map of the Familial Mediterranean Fever candidate region allows identification of Haplotype-sharing among ethnic groups (1997)

Balow, J. E., Shelton, D. A., Orsborn, A., Mangelsdorf, Marie Elise, Aksentijevich, I., ...

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat (1997)

Yu, S., Mangelsdorf, Marie Elise, Hewett, D., Hobson, L., Baker, E., Eyre, H. J., ...

Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2 (1997)

Horwitz, M., Benson, K. F., Li, F-Q., Wolff, J., Leppert, M. F., Hobson, L., ...

Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever (1997)

Aksentijevich, I., Centola, M., Deng, Z., Sood, R., Balow, J. E., ...

Human chromosomal fragile site FRA16B is an amplified AT-Rich minisatellite repeat (1997)

Yu, S., Mangelsdorf, Marie Elise, Hewett, D., Hobson, L., Baker, E., Eyre, H. J., ...

Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the Familial Mediterranean Fever Locus (MEFV) on chromosome 16p13.3 (1997)

Sood, R., Blake, T., Aksentijevich, I., Wood, G., Chen, X., Gardner, D., ...

A high-resolution genetic map of the Familial Mediterranean Fever candidate region allows identification of Haplotype-sharing among ethnic groups (1997)

Balow, J. E., Shelton, D. A., Orsborn, A., Mangelsdorf, Marie Elise, Aksentijevich, I., ...

Dynamic Mutation Loci - Allele Distributions in Different Populations (1996)

Richards, Robert Ian, Crawford, J., Narahara, K., Mangelsdorf, Marie Elise, Friend, K., Staples, A., ...

Dynamic mutation loci: allele distributions in different populations (1996)

Richards, R. I., Crawford, J., Narahara, K., Mangelsdorf, Marie Elise, Friend, K., Staples, A., ...

Dynamic Mutation Loci - Allele Distributions in Different Populations (1996)

Richards, R. I., Crawford, J., Narahara, K., Mangelsdorf, Marie Elise, Friend, K., Staples, A., ...

Dynamic mutation loci: allele distributions in different populations (1996)

Richards, R. I., Crawford, J., Narahara, K., Mangelsdorf, Marie Elise, Friend, K., Staples, A., ...