A. Speer

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Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se

U. Lass, K. Kreuzer, C. Schmidt, 2000, Journal of Molecular Medicine.

Functional Characterization of Atherosclerosis-Associated Ser128Arg and Leu554Phe E-Selectin Mutations

G. Baumann, S. Felix, A. Scheer, 1999, Biological chemistry.

Relationship of polymorphisms in the renin-angiotensin system and in E-selectin of patients with early severe coronary heart disease

G. Baumann, S. Felix, K. Rohde, 1997, Journal of Molecular Medicine.

Antisense oligonucleotides and short interfering RNAs silencing the cyclin-dependent kinase inhibitor p21 improve proliferation of Duchenne muscular dystrophy patients’ primary skeletal myoblasts

Hanns Lochmüller, S. Endesfelder, A. Moers, 2004, Journal of Molecular Medicine.

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

B. Uhlenberg, I. Koch, A. Moers, 2003, Human Genetics.

Examination of Telomere Lengths in Muscle Tissue Casts Doubt on Replicative Aging as Cause of Progression in Duchenne Muscular Dystrophy

K. Oexle, A. Kohlschütter, A. Speer, 1997, Pediatric Research.

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study

A. Covone, C. Broeckhoven, K. Bushby, 2004, Human Genetics.

Polymorphism in the human E-selectin gene detected by PCR-SSCP

A. Speer, K. Wenzel, R. Hanke, 1994, Human Genetics.

A small in‐frame deletion within the protease domain of muscle‐specific calpain, p94 causes early‐onset limb‐girdle muscular dystrophy 2A

C. Hübner, T. Voit, K. Oexle, 1998 .

Genomic organization of the human excitatory amino acid transporter gene GLT‐1

A. Ludolph, T. Meyer, C. Hagemeier, 1997, Neuroreport.

The glial glutamate transporter complementary DNA in patients with amyotrophic lateral sclerosis

A. Ludolph, T. Meyer, W. Sitte, 1996, Annals of neurology.

Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosis

A. Weindl, A. Ludolph, T. Meyer, 1995, Annals of neurology.

CCA paper: a new two-dimensional cyanuric chloride-activated matrix for universal application in molecular biology.

C. Coutelle, P. Franke, R. Szargan, 1986, Analytical biochemistry.

Typing of families with classical phenylketonuria using three alleles of the Hindlll linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe

O. Riess, R. Cotton, H. Dahl, 1986 .

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy

T. Braun, D. Mennerich, M. Schuelke, 2000, Neuromuscular Disorders.

Sequences of junction fragments in the deletion-prone region of the dystrophin gene.

K. Davies, R. Mountford, D. Love, 1991, Genomics.

Wheat Kernel Ingestion Protects from Progression of Muscle Weakness in mdx Mice, an Animal Model of Duchenne Muscular Dystrophy

H. Lehr, S. Marklund, T. Voit, 1996, Pediatric Research.

Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP.

O. Riess, R. Cotton, H. Dahl, 1986, Clinical genetics.

Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic Republic

O. Riess, C. Coutelle, A. Speer, 1987, Clinical genetics.

Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysis

O. Riess, C. Coutelle, A. Speer, 1986, Prenatal diagnosis.

Carrier detection in DMD families with point mutations, using PCR-SSCP and direct sequencing

A. Speer, U. Lenk, R. Hanke, 1994, Neuromuscular Disorders.

Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic Republic

O. Riess, C. Coutelle, A. Speer, 1988, Human Genetics.

The isolation of a clone for human α 1-antitrypsin and the detection of α 1-antitrypsin in mRNA from liver and leukocytes

J. Rogers, S. Humphries, N. Kalsheker, 1983 .

A cysteine 3340 substitution in the dystroglycan-binding domain of dystrophin associated with Duchenne muscular dystrophy, mental retardation and absence of the ERG b-wave.

C. Hübner, T. Voit, K. Oexle, 1996, Human molecular genetics.

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients.

H. Thiele, H. Thiele, A. Speer, 1993, Human molecular genetics.

Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiency.

M. Schuelke, E. Mayatepek, B. Finckh, 1999, The Journal of pediatrics.

A common base change in the promoter region of the human endothelial NO‐synthase (NQS3) gene

C. Opitz, A. Speer, F. Kleber, 1996, Human mutation.

Petri net modelling of gene regulation of the Duchenne muscular dystrophy

Ina Koch, Stefanie Grunwald, Astrid Speer, 2008, Biosyst..

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

K. Fischbeck, K. Davies, S. Kenwrick, 1987, Cell.

Mapping of a human rRNA gene in the YAC contig surrounding the SMA candidate gene

A. Katzer, A. Gasch, J. Huschenbett, 1995, Human Genetics.

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

K. Davies, J. Burn, S. Forrest, 1987, Nature.

Transfection of normal primary human skeletal myoblasts with p21 and p57 antisense oligonucleotides to improve their proliferation: a first step towards an alternative molecular therapy approach of Duchenne muscular dystrophy

R. Reszka, S. Endesfelder, A. Speer, 2003, Journal of Molecular Medicine.

Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin gene.

I. Grunewald, U Lenk, R Hanke, 1993, Journal of medical genetics.

Human X chromosome markers and Duchenne muscular dystrophy.

K. Davies, V. Steinbicker, M. Schwartz, 1985, Nucleic acids research.

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.

K. Davies, K. Robson, S. Forrest, 1988, Genomics.

RELP-discordance within the human phenylalanine hydroxylase locus

W. Berger, O. Riess, P. Nürnberg, 1989, Human Genetics.

Crossovers in two German cystic fibrosis families determine probe order for MET, 7C22 and XV-2c/CS.7

M. Farrall, R. Williamson, C. Coutelle, 1987, Human Genetics.

DMA polymorphisms in adhesion molecule genes — a new risk factor for early atherosclerosis

K. Rohde, A. Speer, K. Wenzel, 2004, Human Genetics.

Deletion analysis of DMD/BMD families from the German Democratic Republic and selected regions of Czechoslovakia and Hungary.

L. Kádasi, C. Coutelle, K. Wulff, 1990, Journal of medical genetics.

Genomics in the German Democratic Republic.

C. Coutelle, A. Speer, 1990, Genomics.

DNA Analysis of Duchenne and Becker Muscular Dystrophies

K. Davies, S. Kenwrick, C. Coutelle, 1986 .

Molecular analysis of Duchenne and Becker muscular dystrophies.

K. Davies, S. Forrest, D. Love, 1989, British medical bulletin.

Present state of DNA-diagnosis for cystic fibrosis and attitudes concerning a heterozygote screening in the GDR.

V. Steinbicker, K. Will, C. Coutelle, 1991, Advances in experimental medicine and biology.

Polymerase chain reaction for detection of the pMP6d-9/MspI RFLP, a marker closely linked to the cystic fibrosis mutation.

X. Estivill, C. Coutelle, M. Ramsay, 1989, Nucleic acids research.

Prenatal diagnosis of the acute form of proximal spinal muscular atrophy: Experience on the acceptance of linkage analyses by the families

J. Huschenbett, A. Speer, R. Hanke, 1993, Prenatal diagnosis.

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

K. Davies, A. Read, T. Flint, 1988, Journal of medical genetics.

Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.

D. Hill, K. Davies, S. Forrest, 1987, The EMBO journal.

Four new polymorphisms in the human dystrophin gene from an Argentinian population

S. Baranzini, I. Szijan, A. Speer, 1997, Muscle & nerve.

β1-Adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?

R. Hetzer, G. Wallukat, G. Baumann, 2000, Journal of Molecular Medicine.

Beta1-adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?

R. Hetzer, G. Wallukat, J. Müller, 2000, Journal of molecular medicine.

Use of cyanuric chloride-activated paper for detection of subpicogram quantities of specific DNA sequences and its application to linked restriction fragment length polymorphism analysis in a Duchenne muscular dystrophy affected family.

C. Coutelle, C. Flachmeier, A. Speer, 1987, Analytical biochemistry.

Fine mapping of human PI 3-kinase associated p85α transcripts in the YAC contig surrounding the spinal muscular atrophy gene

A. Katzer, A. Gasch, J. Huschenbett, 1994, Human Genetics.

Possibilities and limitations of carrier diagnosis in families with Duchenne muscular dystrophy caused by deletions in the major hot spot region using pulsed-field gel electrophoresis.

J. Huschenbett, A. Volz, A. Speer, 1991, Biomedica biochimica acta.

Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.

K. Davies, S. Kenwrick, C. Coutelle, 1987, Nucleic acids research.

Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.

K. Davies, J. Schieck, S. Forrest, 1989, Journal of medical genetics.

Alternative splicing of dystrophin mRNA complicates carrier determination: report of a DMD family.

A. Speer, S. Demuth, U. Lenk, 1993, Journal of medical genetics.

DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening.

K. Davies, C. Coutelle, S. Forrest, 1989, Nucleic acids research.

Modularization of biochemical networks based on classification of Petri net t-invariants

Andrea Sackmann, Falk Schreiber, Björn H. Junker, 2008, BMC Bioinformatics.