D. Salk

发表

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

Decreased oxygen supply enhances growth in culture of human mid-trimester amniotic fluid cells

M. Kubbies, D. Salk, M. Brackertz, 2004, Human Genetics.

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 cytometric analysis of small DNA content differences in heterogeneous cell populations: human amniotic fluid cells.

P. Rabinovitch, T. Bettecken, J. Smith, 1984, Cytometry.

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.

Detection and Staging of Small Cell Lung Carcinoma with a Technetium‐labeled Monoclonal Antibody A Comparison with Standard Staging Methods

E. Frenkel, J. Cox, D. Salk, 1992, Clinical nuclear medicine.

Staging Lung Carcinoma with a Tc‐99m Labeled Monoclonal Antibody

T. A. Powers, J. Vansant, A. Sonin, 1992, Clinical nuclear medicine.

Werner’s Syndrome and Human Aging

G. Martin, D. Salk, Human Aging, 1985, Advances in Experimental Medicine and Biology.

Role of technetium 99m-labeled monoclonal antibody in the management of melanoma patients.

M. Blend, T. K. Gupta, D. Salk, 1992, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Radionuclide Imaging of Bone Marrow Metastases with a Tc‐99m Labeled Monoclonal Antibody to Small Cell Lung Carcinoma

E. Frenkel, J. Cox, D. Salk, 1991, Clinical nuclear medicine.

Cell fusion studies and biochemical analysis of DNA synthesis in Werner and non-Werner cultured cells.

T. Norwood, W. Pendergrass, D. Salk, 1985, Advances in experimental medicine and biology.

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.

Radioimmunoscintigraphy in patients with early stage cutaneous malignant melanoma.

K. Sullivan, M. Blend, D. Salk, 1996, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Growth characteristics of Werner syndrome cells in vitro.

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

Pseudotumour cerebri and the Turner syndrome.

T. Bird, V. Sybert, D. Salk, 1985, Journal of neurology, neurosurgery, and psychiatry.

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.

Chromosome studies in hemifacial microsomia with radial ray defect.

S. Clarren, D. Salk, 1983, American journal of medical genetics.

Proteoglycans in the Werner syndrome and aging: a review and perspective.

E. Bryant, T. Wight, D. Salk, 1985, Advances in experimental medicine and biology.

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.

Nonfluorescent dicentric Y in males with hypospadias.

R. Pagon, D. Salk, M. Drummond-Borg, 1988, The Journal of pediatrics.

Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations

D. Salk, 2004, Human Genetics.

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

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

Induction of DNA polymerase α in senescent cultures of normal and Werner's syndrome cultured skin fibroblasts

T. Norwood, W. Pendergrass, D. Salk, 1985, Journal of cellular physiology.

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

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

Can We Learn about Aging from a Study of Werner's Syndrome?

D. Salk, 1982, Journal of the American Geriatrics Society.

C. Disteche, A. Nelson, K. Swisshelm, 1990, Mutation research.

Antenatal diagnosis of mosaic trisomy 8 confirmed in fetal tissues

D. Luthy, T. Norwood, K. Swisshelm, 1981, Clinical genetics.

Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.

J. Siebert, D. Salk, C. Bradley, 1987, American journal of medical genetics.

Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3)

C. Disteche, R. E. Kalina, R. Pagon, 2004, Human Genetics.

Mosaicism for ring 19: a case report

V. Sybert, D. Salk, C. Bradley, 1988, Clinical genetics.

Trisomy Xq in a male: the isochromosome X Klinefelter syndrome.

D. Salk, C. Dolan, C. Bradley, 1987, American journal of medical genetics.

In vitro studies of Werner syndrome cells: aberrant growth and chromosome behavior.

D. Salk, 1985, Basic life sciences.

Eighth International Conference on Gene Therapy of Cancer

H. Engler, B. Hutchins, S. Wen, 1999, Cancer Gene Therapy.