H. Hoehn

发表

p53 activates Fanconi anemia group C gene expression.

W. Liebetrau, A. Budde, A. Savoia, 1997, Human molecular genetics.

Modulation of the spontaneous G2 phase blockage in Fanconi anemia cells by caffeine: differences from cells arrested by X-irradiation.

H. Hoehn, H. Seyschab, G. Bretzel, 1994, Mutation research.

Prototype sequence clues within the Fanconi anaemia group C gene.

W. Liebetrau, H. Hoehn, M. Bühner, 1995, Journal of medical genetics.

Genotype-phenotype correlations in Fanconi anemia.

Kornelia Neveling, H. Hoehn, D. Schindler, 2009, Mutation research.

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

M. Poot, H. Hoehn, D. Lessel, 2010, Human Genetics.

Cytogenetic aspects of Werner syndrome.

H. Hoehn, G. Martin, D. Salk, 1985, Advances in experimental medicine and biology.

Fanconi anemia: causes and consequences of genetic instability.

H. Hoehn, D. Schindler, K. Neveling, 2006, Genome dynamics.

Flow-cytogenetics: sources of DNA content variation among euploid individuals.

J. Callis, H. Hoehn, P. Johnston, 1977, Cytogenetics and cell genetics.

Cultivated Cells from Diagnostic Amniocentesis in Second Trimester Pregnancies. I. Clonal Morphology and Growth Potential

H. Hoehn, E. Bryant, G. Martin, 1974, Pediatric Research.

Response to X-Irradiation of Fanconi Anemia Homozygous and Heterozygous Cells Assessed by the Single-Cell Gel Electrophoresis (Comet) Assay

H. Hoehn, D. Schindler, M. Flentje, 2001, Laboratory Investigation.

Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction

H. Hoehn, R. Friedl, D. Schindler, 2003, Cytogenetic and Genome Research.

Differential activity of recombinant lymphokines on mouse B cell proliferation and cell cycle progression are revealed by 5‐bromo‐2′‐deoxyuridine/Hoechst 33258 dye flow cytometry

P. Rabinovitch, H. Hoehn, H. Seyschab, 1991, European journal of immunology.

The effects of bacterial lipopolysaccharide, anti‐receptor antibodies and recombinant interferon on mouse B cell cycle progression using 5‐bromo‐2'‐deoxyuridine/hoechst 33258 dye flow cytometry

P. Rabinovitch, H. Hoehn, H. Seyschab, 1989, European journal of immunology.

Interphase cell flow cytometry as a means of monitoring genomic size in normal and neoplastoid cell cultures.

P. Rabinovitch, H. Hoehn, T. Bettecken, 1987, Cancer genetics and cytogenetics.

Flow-fluorometric diagnosis of euploid and aneuploid human lymphocytes.

J. Callis, H. Hoehn, 1976, American journal of human genetics.

Variegated translocation mosaicism in human skin fibroblast cultures.

H. Hoehn, T. Norwood, E. Bryant, 1975, Cytogenetics and cell genetics.

Evidence of clonal attenuation, clonal succession, and clonal expansion in mass cultures of aging Werner's syndrome skin fibroblasts.

H. Hoehn, G. Martin, D. Salk, 1981, Cytogenetics and cell genetics.

Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells.

P. Rabinovitch, H. Hoehn, D. Schindler, 1985, American journal of human genetics.

Fanconi anemia mutation causes cellular susceptibility to ambient oxygen.

H. Hoehn, D. Schindler, 1988, American journal of human genetics.

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype.

G. Pals, J. Soulier, J. Surrallés, 2007, American journal of human genetics.

Milestones in Fanconi Anemia Research

H. Hoehn, K. Sperling, M. Digweed, 2007 .

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

G. Pals, R. Gibson, J. Cavenagh, 1999, European Journal of Human Genetics.

New mutations in the ataxia telangiectasia gene

H. Hoehn, D. Schindler, A. Baumer, 1996, Human Genetics.

Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport.

C. Mathew, Q. Waisfisz, H. Hoehn, 2003, Experimental cell research.

The minor-groove binding DNA-ligands netropsin, distamycin A and berenil cause polyploidisation via impairment of the G2 phase of the cell cycle.

M. Poot, T. Haaf, H. Hoehn, 1990, Cell structure and function.

Disturbance of cell proliferation by two model compounds of lipid peroxidation contradicts causative role in proliferative senescence

M. Poot, P. Rabinovitch, H. Hoehn, 1988, Journal of cellular physiology.

Free radical mediated cytotoxicity of desferrioxamine.

M. Poot, P. Rabinovitch, H. Hoehn, 1989, Free radical research communications.

Characterzation of a newly established human urinary bladder cancer cell line (BT-1)

H. Hoehn, J. Köhler, W. Heckl, 2004, Urological Research.

Cell cycle analysis using continuous bromodeoxyuridine labeling and Hoechst 33258-ethidium bromide bivariate flow cytometry.

M. Poot, P. Rabinovitch, H. Hoehn, 1990, Methods in cell biology.

Cell-cycle analysis using continuous bromodeoxyuridine labeling and Hoechst 33358-ethidium bromide bivariate flow cytometry.

M. Poot, P. Rabinovitch, H. Hoehn, 1994, Methods in cell biology.

Synkaryon and Heterokaryon Analyses of Clonal Senescence

H. Hoehn, T. Norwood, G. Martin, 1977 .

Cultivated cells from mid‐trimester amniotic fluids. IV. Cell type identification via one and two‐dimensional electrophoresis of clonal whole cell homogenates

H. Hoehn, G. Martin, D. Salk, 1982, Prenatal diagnosis.

Effects of chromosome constitution on growth and longevity of human skin fibroblast cultures.

P. Rabinovitch, H. Hoehn, E. Bryant, 1980, American journal of medical genetics.

Genetics and human disease.

H. Hoehn, G. Martin, 1974, Human pathology.

Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes

F. Hanefeld, I. Krägeloh-Mann, J. Fryns, 1992, European Journal of Pediatrics.

Interphase flow-cytogenetics: Correlation of DNA fluorescence to aneuploidy in human fibroblast cultures

P. Rabinovitch, H. Hoehn, G. Martin, 1982, Human Genetics.

Small structural changes of chromosome 8

H. Hoehn, J. Hall, J. Hanson, 1977, Human Genetics.

No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45 XO Turner syndrome

J. Callis, H. Hoehn, J. Burns, 1979, Clinical genetics.

Growth characteristics of Werner syndrome cells in vitro.

H. Hoehn, E. Bryant, G. Martin, 1985, Advances in experimental medicine and biology.

Radiation‐induced DNA damage and repair in peripheral blood mononuclear cells from Nijmegen breakage syndrome patients and carriers assessed by the Comet assay

E. Seemanová, H. Hoehn, D. Schindler, 2006, Environmental and molecular mutagenesis.

Effects of radical-scavenging enzymes and reduced oxygen exposure on growth and chromosome abnormalities of Werner syndrome cultured skin fibroblasts

H. Hoehn, G. Martin, D. Salk, 2004, Human Genetics.

Clonal analysis of stable chromosome rearrangements in Bloom's syndrome fibroblasts.

H. Hoehn, D. Salk, 1984, Cancer genetics and cytogenetics.

Revertant Mosaicism in Fanconi Anemia: Natural Gene Therapy at Work

H. Hoehn, R. Friedl, D. Schindler, 2007 .

Evidence against somatic mutation as a mechanism of clonal senescence.

H. Hoehn, E. Bryant, G. Martin, 1980, Advances in experimental medicine and biology.

DNA topoisomerases and the DNA lesion in human genetic instability syndromes.

M. Poot, H. Hoehn, 1993, Toxicology letters.

Lack of Sensitivity of Primary Fanconi's Anemia Fibroblasts to UV and Ionizing Radiation

H. Hoehn, D. Schindler, H. Joenje, 2004, Radiation research.

Variable response to the diepoxybutane test in two dizygotic twins with Fanconi's anemia and flow cytometry for diagnosis confirmation.

H. Hoehn, B. Porfirio, V. Pistoia, 1998, Pediatric hematology and oncology.

Cytostatic synergism between bromodeoxyuridine, bleomycin, cisplatin and chlorambucil demonstrated by a sensitive cell kinetic assay.

M. Poot, H. Hoehn, A. Schuster, 1991, Biochemical pharmacology.

The Fanconi anaemia group G gene FANCG is identical with XRCC9

Hans Joenje, Johan P. de Winter, Quinten Waisfisz, 1998, Nature Genetics.

Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia.

H. Hoehn, H. Seyschab, R. Friedl, 1995, Blood.

Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism.

H. Hoehn, G. Martin, D. Salk, 1981, Cytogenetics and cell genetics.

Morphological and biochemical heterogeneity of amniotic fluid cells in culture.

H. Hoehn, D. Salk, 1982, Methods in cell biology.

Do hyperplastoid cell lines "differentiate themselves to death"?

H. Hoehn, T. Norwood, P. Bornstein, 1975, Advances in experimental medicine and biology.

Cytogenetic studies on cultured fibroblast‐like cells derived from basal cell carcinoma tissue

R. Happle, H. Hoehn, Rudolf Happle, 1973, Clinical genetics.

PRESYMPTOMATIC DIAGNOSIS OF FANCONI'S ANAEMIA

P. Rabinovitch, H. Hoehn, D. Schindler, 1985, The Lancet.

Cell kinetic evidence suggests elevated oxidative stress in cultured cells of Bloom's syndrome.

M. Poot, T. Nicotera, H. Hoehn, 1989, Free radical research communications.

Melanoma-inhibiting activity inhibits cell proliferation by prolongation of the S-phase and arrest of cells in the G2 compartment.

U. Bogdahn, M. Poot, H. Hoehn, 1990, Cancer research.

Normalisation of sister chromatid exchange frequencies in Bloom's syndrome by euploid cell hybridisation

H. Hoehn, G. Martin, Eileen M. Bryant, 1979, Nature.

Regulation of growth and gene activity in euploid hybrids between human neonatal fibroblasts and epithelioid amniotic fluid cells.

H. Hoehn, P. Bornstein, E. Bryant, 1978, American journal of human genetics.

Heterogeneity of bromodeoxyuridine sensitivity of cultured cells from melanoma metastases.

M. Poot, H. Hoehn, S. Heimpel, 1995, Cytometry.

Bromodeoxyuridine amplifies free-radical-mediated DNA damage.

M. Poot, P. Rabinovitch, H. Hoehn, 1989, The Biochemical journal.

Bromodeoxyuridine amplifies the inhibitory effect of oxygen on cell proliferation.

M. Poot, P. Rabinovitch, H. Hoehn, 1988, Cytometry.

BrdU-Hoechst flow cytometry: a unique tool for quantitative cell cycle analysis.

P. Rabinovitch, H. Hoehn, D. Schindler, 1988, Experimental cell research.

Cultivated cells from diagnostic amniocentesis in second trimester pregnancies

H. Hoehn, A. Fantel, E. Bryant, 1975, Humangenetik.

Amniotic Fluid Cell Culture

H. Hoehn, 1986 .

Disruption of the FA/BRCA pathway in bladder cancer

M. Schmid, C. Steinlein, M. Schmid, 2007, Cytogenetic and Genome Research.

In vitro alteration of association patterns of human acrocentric chromosomes

H. Hoehn, W. Krone, M. Nagel, 2004, Humangenetik.

Heritable alteration of human constitutive heterochromatin induced by mitomycin C.

H. Hoehn, G. Martin, 1972, Experimental cell research.

Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes.

R. Pagon, H. Hoehn, T. Norwood, 1979, American journal of human genetics.

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

Effects of cytochalasin B on cultivated human diploid fibroblasts and its use for the isolation of tetraploid clones.

H. Hoehn, G. Martin, C. Sprague, 1973, Experimental cell research.

Cellular aging in Werner's syndrome: a unique phenotype?

H. Hoehn, T. Norwood, G. Martin, 1979, The Journal of investigative dermatology.

Trisomy of the long arm of human chromosome 1

H. Hoehn, T. Norwood, 1974, Humangenetik.

Functional implications of differential chromosome banding.

H. Hoehn, 1975, American journal of human genetics.

Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts

H. Hoehn, E. Bryant, D. Salk, 2004, Human Genetics.

PLOIDY OF LIVING CLONES OF HUMAN SOMATIC CELLS DETERMINED BY MENSURATION AT METAPHASE

H. Hoehn, G. Martin, C. Sprague, 1974, The Journal of cell biology.

Genetic studies on a minute centric fragment transmitted through three generations.

H. Hoehn, W. Engel, H. Reinwein, 1970, Cytogenetics.

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

B. Dutrillaux, H. Hoehn, J. Lejeune, 1973, Humangenetik.

Mutagenic activity of ambient oxygen and mitomycin C in Fanconi's anaemia cells.

M. Poot, W. Liebetrau, H. Hoehn, 1997, Mutagenesis.

More on marker X chromosomes, mental retardation and macro-orchidism.

P. Jacobs, H. Hoehn, E. Rudak, 1979, The New England journal of medicine.

Induction of replicative senescence by 5‐azacytidine: fundamental cell kinetic differences between human diploid fibroblasts and NIH‐3T3 cells

M. Poot, H. Hoehn, E. Weller, 1993, Cell proliferation.

Prenatal genetic diagnosis and elective abortion in women over 35: utilization and relative impact on the birth prevalence of Down syndrome in Washington State.

D. Luthy, H. Hoehn, J. Hall, 1980, American journal of medical genetics.

Fragile X expression studied by clonal analysis and somatic cell hybridization.

H. Hoehn, E. Bryant, G. Martin, 1983, Cytogenetics and cell genetics.

Localisation of a Fanconi anaemia gene to chromosome 9p

T. Wienker, H. Hoehn, R. Wegner, 1998, European Journal of Human Genetics.

Diploid-triploid mixoploidy: clinical and cytogenetic aspects.

J. Graham, H. Hoehn, M. S. Lin, 1981, Pediatrics.

Mosaicism in amniotic fluid cell cultures: classification and significance.

H. Hoehn, T. Norwood, C. Maxwell, 1978, American journal of medical genetics.

The replicative life spans of euploid hybrids derived from short-lived and long-lived human skin fibroblast cultures.

H. Hoehn, E. Bryant, G. Martin, 1978, Cytogenetics and cell genetics.

Non-selective isolation, stability and longevity of hybrids between normal human somatic cells

H. Hoehn, T. Norwood, P. Johnston, 1975, Nature.

Genetic instability and fanconi anemia

H. Hoehn, D. Schindler, A. Sobeck, 2003 .

Cell cycle defect in connection with oxygen and iron sensitivity in Fanconi anemia lymphoblastoid cells.

M. Poot, H. Hoehn, B. Epe, 1996, Experimental cell research.

Exploring the role of oxygen in Fanconi's anemia.

M. Poot, W. Liebetrau, H. Hoehn, 1997, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

The spectrum of WRN mutations in Werner syndrome patients

Markus Schuelke, Thomas Dorn, Johannes Ring, 2006, Human mutation.

Postnatal Confirmation of Prenatally Diagnosed Trisomy 20 Mosaicism in a Patient with Linear and Whorled Nevoid Hypermelanosis

H. Hoehn, H. Hamm, A. Hartmann, 2004, Pediatric dermatology.

Identification of ataxia telangiectasia heterozygotes, a cancer-prone population, using the single-cell gel electrophoresis (Comet) assay.

H. Hoehn, D. Schindler, M. Flentje, 1999, Laboratory investigation; a journal of technical methods and pathology.

Chromosome 7 short arm deletion and craniosynostosis a 7p-syndrome

H. Hoehn, T. Norwood, E. McPherson, 1976, Human Genetics.

Continuous bromodeoxyuridine labeling and bivariate ethidium bromide/Hoechst flow cytometry in cell kinetics.

M. Poot, P. Rabinovitch, H. Hoehn, 1989, Cytometry.

Cell Cycle Kinetics By Brdu‐Hoechst Flow Cytometry: an Alternative to the Differential Metaphase Labelling Technique

P. Rabinovitch, H. Hoehn, D. Schindler, 1985, Cell and tissue kinetics.

Prenatal diagnosis of human genome variation.

H. Hoehn, D. Kurnit, D M Kurnit, 1979, Annual review of genetics.

A Chromosome 13q+in a patient with characteristics of the trisomy 13 syndrome

H. Hoehn, U. Wolf, H. Wehinger, 2004, Humangenetik.

Applications of Cell Cycle Testing in Fanconi Anemia

H. Hoehn, R. Friedl, D. Schindler, 2007 .

Genetic instability syndromes with progeroid features

H. Hoehn, K. Neveling, A. Bechtold, 2007, Zeitschrift für Gerontologie und Geriatrie.

Flow Cytometric Testing for Syndromes with Chromosomal Instability, Aplastic Anemia and Related Hematological Disorders

H. Hoehn, D. Schindler, 1999 .

Confounding factors in the diagnosis of Fanconi anaemia.

H. Hoehn, H. Joenje, F. Arwert, 1998, American journal of medical genetics.

Exclusion/confirmation of Ataxia-telangiectasia via cell-cycle testing

H. Hoehn, R. Friedl, D. Schindler, 2006, European Journal of Pediatrics.

Prenatal Exclusion/Confirmation of Fanconi Anemia via Flow Cytometry: A Pilot Study

H. Hoehn, R. Friedl, D. Schindler, 2005, Fetal Diagnosis and Therapy.

G2 phase cell cycle disturbance as a manifestation of genetic cell damage

H. Hoehn, H. Seyschab, R. Friedl, 1993, Human Genetics.

BrdU-Hoechst Flow Cytometry Links the Cell Kinetic Defect of Fanconi Anemia to Oxygen Hypersensitivity

M. Poot, P. Rabinovitch, H. Hoehn, 1989 .

Nonrandom arrangement of human chromatin: topography of disomic markers X, Y, and 1h plus 1.

H. Hoehn, G. Martin, 1973, Cytogenetics and cell genetics.

Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell lines.

M. Poot, H. Hoehn, G. Martin, 1992, Experimental cell research.

Human Aging and Longevity: Genetic Aspects

H. Hoehn, A. Renner, 2003 .

Clonal variants of constitutive heterochromatin of human fibroblasts after recovery from mitomycin treatment

H. Hoehn, G. Martin, 1973, Chromosoma.

Detection of free radical-induced DNA damage with bromodeoxyuridine/Hoechst flow cytometry: implications for Bloom's syndrome.

M. Poot, H. Hoehn, H. Rüdiger, 1990, Mutation research.

DNA ploidy and cell‐cycle analysis in intracranial meningiomas and hemangiopericytomas: A study with high‐resolution DNA flow cytometry

J. Meixensberger, H. Hoehn, W. Roggendorf, 1998, International journal of cancer.

Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation

H. Hoehn, W. Engel, H. Reinwein, 2004, Humangenetik.

Cell cycle effects of the DNA topoisomerase inhibitors camptothecin and m-AMSA in lymphoblastoid cell lines from patients with Fanconi anemia.

M. Poot, H. Hoehn, B. Epe, 1992, Mutation research.

CD8+CD45RA+CD27-CD28-T-cell subset in PBL of cervical cancer patients representing CD8+T-cells being able to recognize cervical cancer associated antigens provided by HPV 16 E7

R. Seufert, E. Steiner, H. Pilch, 2002, Zentralblatt fur Gynakologie.

Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

H. Hoehn, J. Hall, M. Jennings, 1980, American journal of medical genetics.

Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.

G. Schellenberg, E. Wijsman, T. Ogihara, 1994, American journal of human genetics.

Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure

Raymonda Varon, H. Hoehn, D. Schindler, 2007, Orphanet journal of rare diseases.

Somatic stability of variant C-band heterochromatin

H. Hoehn, L. Karp, K. Au, 1977, Human Genetics.

Aneusomie de recombinaison: rearrangement between paternal chromosomes 4 and 18 yielding offspring with features of the 18q- syndrome.

H. Hoehn, C. Sander, L. Sander, 1971, Annales de genetique.

Screening for minute deletions in patients with suspected cri-du-chat syndrome and apparently normal karyotype

H. Hoehn, W. Engel, 1969, Humangenetik.

On the non-random involvement of D-group chromosomes in centric fusion translocations in man

H. Hoehn, M. Nagel, 2004, Humangenetik.

Clinical Investigation

A. Rosenthal, M. Platzer, H. Hoehn, 2003, Advances in Experimental Medicine and Biology.

Xavier Rogiers, A. Geerts, I. Colle, 2013, Hepatology research : the official journal of the Japan Society of Hepatology.

Characterization of a Newly Established Human Urinary Bladder Cancer Cell Line (BT-1)

H. Hoehn, J. Köhler, W. Heckl, 1988 .

SCREENING TEST FOR ATAXIA TELANGIECTASIA

M. Poot, P. Rabinovitch, N. Tommerup, 1987, The Lancet.

BrdU‐Hoechst flow cytometry reveals regulation of human lymphocyte growth by donor‐age–related growth fraction and transition rate

P. Rabinovitch, H. Hoehn, D. Schindler, 1985, Journal of cellular physiology.

Spectral karyotyping of Werner syndrome fibroblast cultures

C. Steinlein, M. Schmid, H. Hoehn, 2000, Cytogenetic and Genome Research.

Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system.

H. Hoehn, S. Herterich, T. Reuter, 2000, Blood.

Cultivated cells from diagnostic amniocentesis in second trimester pregnancies

H. Hoehn, E. Bryant, G. Martin, 1975, Clinical genetics.

Response to the letters of Drs. Seabright, Feeny, and Tomkins

H. Hoehn, N. Fisher, 1981 .

The fate of the primary diploid population during spontaneous transformation of growth factor-supplemented murine cell cultures.

H. Hoehn, R. Friedl, T. Bettecken, 1986, Cytometry.

Ultrasonic Placental Localization and Bloody Taps in Midtrimester Amniocentesis for Prenatal Genetic Diagnosis

H. Hoehn, D. Hickok, L. Karp, 1977, Obstetrics and gynecology.

Partial correction of chromosome instability in Fanconi anemia by desferrioxamine

H. Hoehn, Martin Foot, 2004, Human Genetics.

Amniotic fluid cell mosaicism for presumptive trisomy 20

D. Luthy, H. Hoehn, T. Norwood, 1978, Clinical genetics.

Prenatal diagnosis of chromosomal mosaicism for trisomy D.

H. Hoehn, J. Hall, F. Dill, 1977, The Journal of pediatrics.

Trisomy 3 (p23-pter) resulting from maternal translocation, t (3 ; 4)(p23 ; q35).

R. Pagon, H. Hoehn, A. Schinzel, 1978, Annales de Genetique.

Characteristics of homogeneously small keratinocytes from newborn rat skin: possible epidermal stem cells.

M. Poot, H. Hoehn, P. Jaffray, 1991, The American journal of physiology.

Distinct patterns of cell cycle disturbance elicited by compounds interfering with DNA topoisomerase I and II activity.

M. Poot, H. Hoehn, S. Heimpel, 1995, Experimental Cell Research.

Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging

H. Hoehn, D. Schindler, 2007 .

Improvement of human lymphocyte proliferation and alteration of IL-2 secretion kinetics by alpha-thioglycerol.

P. Rabinovitch, H. Hoehn, R. Friedl, 1990, Lymphokine research.

Confirmation of Fanconi's Anemia and Detection of a Chromosomal Aberration (1Q12–32 Triplication) Via BRDU/Hoechst Flow Cytometry

P. Rabinovitch, H. Hoehn, D. Schindler, 1987, The American journal of pediatric hematology/oncology.

Cell size and RNA content correlate with cell differentiation and proliferative capacity of rat keratinocytes

M. Poot, H. Hoehn, M. Rizk-Rabin, 1990, Journal of cellular physiology.