M. Altherr

发表

The DNA sequence and comparative analysis of human chromosome 5

Paul Richardson, Jan-Fang Cheng, Steve Lowry, 2004, Nature.

The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p.

M. MacDonald, H. Lehrach, J. Gusella, 1992, Genomics.

Genomics of the group of organisms

J. Ravel, D. Rasko, Cliff Han, 2005 .

First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation.

H. Dörr, A. Reis, A. Rauch, 2001, American journal of medical genetics.

Plasmid vectors for the analysis of regulatory sequences in yeast.

R. Rodriguez, M. Altherr, 1988, Biotechnology.

Cloning and chromosomal localization of two novel human genes encoding LIM-domain binding factors CLIM1 and CLIM2/LDB1/NLI

J. Murray, M. Altherr, E. Semina, 1998, Mammalian Genome.

Actinin-associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs

W. Kuo, D. Bredt, H. Xia, 1997, The Journal of cell biology.

The Complete Genome Sequence of Bacillus thuringiensis Al Hakam

Lynne A. Goodwin, J. Longmire, N. Doggett, 2007, Journal of bacteriology.

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.

E. Haan, G. Sutherland, O. Riess, 1997, American journal of medical genetics.

Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3).

J. Nadeau, J. Wasmuth, M. Altherr, 1992, Genomics.

A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).

A. Chakravarti, M. Altherr, S. Winokur, 1993, American journal of human genetics.

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

M. Pericak-Vance, C. Wijmenga, R. Griggs, 1993, Nature Genetics.

The DNA sequence and biology of human chromosome 19

Terrence S. Furey, Inna Dubchak, Matt Nolan, 2004, Nature.

The sequence and analysis of duplication-rich human chromosome 16

Judith D. Cohn, Paul Richardson, Steve Lowry, 2004, Nature.

Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy

U. Bengtsson, M. Altherr, S. Winokur, 1995, Muscle & nerve. Supplement.

Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophy

R. Griggs, T. Feasby, M. Altherr, 1993, Human mutation.

A highly polymorphic VNTR locus on the long arm of chromosome 4.

Y. Nakamura, R. White, J. Wasmuth, 1991, Nucleic acids research.

Genomics of the Bacillus cereus group of organisms.

David A Rasko, Jacques Ravel, J. Ravel, 2005, FEMS microbiology reviews.

A YAC contig spanning a cluster of human type III receptor protein tyrosine kinase genes (PDGFRA-KIT-KDR) in chromosome segment 4q12.

D. Le Paslier, D. Ward, R. Spritz, 1994, Genomics.

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.

A. Battaglia, R. Tenconi, G. Neri, 2000, American journal of medical genetics.

A novel G protein-coupled receptor kinase gene cloned from 4p16.3.

D. Church, M. MacDonald, C. Ambrose, 1992, Human molecular genetics.

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.

D. Ledbetter, J. Gusella, J. Wasmuth, 1991, American journal of human genetics.

Assignment of the human gene encoding eukaryotic initiation factor 4E (EIF4E) to the region q21-25 on chromosome 4

M. MacDonald, D. Louis, E. Schmidt, 1997, Somatic cell and molecular genetics.

The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library.

J. Gusella, G. Bates, J. Wasmuth, 1993, Human molecular genetics.

Bone morphogenetic protein: chromosomal localization of human genes for BMP1, BMP2A, and BMP3.

J. McPherson, B. Emanuel, J. Wasmuth, 1991, Genomics.

In situ studies with membrane diffusion chambers of antibiotic resistance transfer in Escherichia coli

M. Altherr, K. L. Kasweck, 1982, Applied and environmental microbiology.

Comparative analysis of a novel gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks syndrome critical region.

M. Altherr, P. Francis-West, C. Naranjo, 1999, Genomics.

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma.

A. Moorman, P. D. de Boer, J. T. Dunnen, 1998, Human molecular genetics.

Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions.

M. Altherr, O. Quarrell, M. Clemens, 1998, American journal of medical genetics.

Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs.

V. P. Johnson, M. Altherr, A. V. Perez-Castro, 1997, American journal of medical genetics.

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region.

E. Zackai, N. Spinner, K. Hirschhorn, 1997, Human molecular genetics.

Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndrome.

V. P. Johnson, J. Gusella, J. Wasmuth, 1992, American journal of medical genetics.

Genetic and physical maps of human chromosome 4 based on dinucleotide repeats.

K H Buetow, J C Murray, J. Weber, 1992, Genomics.

The complete sequence of human chromosome 5

Martin J. Pollard, E. Eichler, R. Myers, 2004 .

An integrated physical map of human chromosome 16.

N. Doggett, D. C. Bruce, B. Marrone, 1995, Nature.

Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13.1-q21.1 and mouse chromosome 5.

D. Beier, M. Altherr, U. Kaiser, 1994, Genomics.

J. McPherson, P. Meltzer, G. Nabel, 1992, Genomics.

The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region.

J. Wasmuth, U. Bengtsson, M. Altherr, 1996, Human molecular genetics.

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease

K. Mathews, J. Wasmuth, J. Murray, 1994, Chromosome Research.

Pathogenomic Sequence Analysis of Bacillus cereus and Bacillus thuringiensis Isolates Closely Related to Bacillus anthracis

Lynne A. Goodwin, J. Longmire, N. Doggett, 2006, Journal of bacteriology.

High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.

J. Wasmuth, U. Bengtsson, M. Altherr, 1994, Human molecular genetics.

Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region

A. Monaco, D. Bentley, D. Paslier, 1992, Nature Genetics.

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4.

D. Housman, J. Gusella, L. Thompson, 1991, Genomics.

Reduced penetrance of the Huntington's disease mutation.

M. MacDonald, J. Gusella, R. Myers, 1997, Human molecular genetics.

Evaluation of the host transcriptional response to human cytomegalovirus infection.

L. M. Rocha, A. Rechtsteiner, R. Gottardo, 2004, Physiological genomics.

Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate region.

F. Collins, M. MacDonald, J. Gusella, 1992, Genomics.

Genomic organization of the human fibroblast growth factor receptor 3 (FGFR3) gene and comparative sequence analysis with the mouse Fgfr3 gene.

M. Altherr, M R Altherr, A V Perez-Castro, 1997, Genomics.

Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a).

J. Gusella, A. Roca, S. Reppert, 1995, Genomics.

Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library.

P. Harper, M. Upadhyaya, J. Maynard, 1995, American journal of medical genetics.

Reply to the letter to the editor by Partington and Turner—“Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes”

K. Hirschhorn, D. Callen, M. Altherr, 1999 .

"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.

M. Altherr, M. Zollino, C. Di Stefano, 1999, American journal of medical genetics.

FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site.

V. P. Johnson, M. Altherr, L. Keppen, 1994, American journal of medical genetics.

Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease gene.

M. MacDonald, J. Wasmuth, L. Hall, 1989, Genomics.

Radiation hybrid map spanning the Huntington disease gene region of chromosome 4.

M. Boehnke, H. Lehrach, J. Gusella, 1992, Genomics.

Genetic mapping of the dentinogenesis imperfecta type II locus.

K H Buetow, J C Murray, C. Wijmenga, 1995, American journal of human genetics.

Primary structure and chromosomal localization of human and mouse rod photoreceptor cGMP-gated cation channel.

M. Seldin, J. Wasmuth, R. Hurwitz, 1992, The Journal of biological chemistry.

Human chromosomal localization of genes encoding the gamma 1 and gamma 2 subunits of the gamma-aminobutyric acid receptor indicates that members of this gene family are often clustered in the genome.

J. Sikela, J. Warrington, J. Wasmuth, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Cloning of the α–adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification

D. Church, D. Housman, R. Snell, 1992, Nature Genetics.

Localization of the D5 dopamine receptor gene to human chromosome 4p15.1-p15.3, centromeric to the Huntington's disease locus.

J. McPherson, G. Evans, J. Wasmuth, 1992, Genomics.

New mutations in sporadic cases

R. Griggs, J. Mendell, M. Altherr, 2006 .

Molecular cloning, cDNA structure, and chromosomal localization of the human type II cGMP-dependent protein kinase.

M. Altherr, K. Tasken, R. Solberg, 1996, Biochemical and biophysical research communications.

Detection by PCR of the VNTR polymorphism at D4S95.

J. Wasmuth, M. Altherr, A. McClatchey, 1991, Nucleic acids research.

Expression capable library for studies of Neisseria gonorrhoeae, version 1.0

G. Weinstock, E. Sodergren, T. Brettin, 2005, BMC Microbiology.

Genomic organization of the mouse fibroblast growth factor receptor 3 (Fgfr3) gene.

M. Altherr, A. V. Perez-Castro, J. Wilson, 1995, Genomics.

Complex patterns of linkage disequilibrium in the Huntington disease region.

M. MacDonald, H. Lehrach, J. Gusella, 1991, American journal of human genetics.

A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat.

A. Pietarinen, S. Knuutila, M. Altherr, 1995, Journal of medical genetics.

Expression capable library for studies of Neisseria gonorrhoeae, version 1.0

G. Weinstock, E. Sodergren, T. Brettin, 2005, BMC Microbiology.

Bmc Microbiology Expression Capable Library for Studies of Neisseria Gonorrhoeae, Version 1.0

G. Weinstock, E. Sodergren, T. Brettin, 2005 .

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus

C. Wijmenga, J. Wasmuth, R. Frants, 1993, Human Genetics.