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Genetics The Genetics collection covers topics such as BRCA, gene therapy, and gene mutations and polymorphisms and includes research articles, case reports, reviews, and editorial commentary.  Subscribe to the Genetics
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1-20 (of 865 results)
| Most recent content (12 May 2008): |
Chromosome 6p22 Locus Associated with Clinically Aggressive Neuroblastoma
Maris J. M., Mosse Y. P., Bradfield J. P., Hou C., Monni S., Scott R. H., Asgharzadeh S., Attiyeh E. F., Diskin S. J., Laudenslager M., Winter C., Cole K. A., Glessner J. T., Kim C., Frackelton E. C., Casalunovo T., Eckert A. W., Capasso M., Rappaport E. F., McConville C., London W. B., Seeger R. C., Rahman N., Devoto M., Grant S. F.A., Li H., Hakonarson H.
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N Engl J Med 2008;
published at www.nejm.org on
May 7, 2008
(10.1056/NEJMoa0708698).
Original Articles
| Earlier content (since Jan 1996): |
Brief Report:An Immunodeficiency Disease with RAG Mutations and Granulomas
Schuetz C., Huck K., Gudowius S., Megahed M., Feyen O., Hubner B., Schneider D. T., Manfras B., Pannicke U., Willemze R., Knüchel R., Göbel U., Schulz A., Borkhardt A., Friedrich W., Schwarz K., Niehues T.
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N Engl J Med 2008;
358:2030-2038, May 8, 2008.
Original Articles
Molecular Origins of Cancer: Tumor Angiogenesis
Kerbel R. S.
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N Engl J Med 2008;
358:2039-2049, May 8, 2008.
Review Articles
A New Weapon for Attacking Tumor Blood Vessels
Semenza G. L.
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N Engl J Med 2008;
358:2066-2067, May 8, 2008.
Clinical Implications of Basic Research
Chromosome 6p22 Locus Associated with Clinically Aggressive Neuroblastoma
Maris J. M., Mosse Y. P., Bradfield J. P., Hou C., Monni S., Scott R. H., Asgharzadeh S., Attiyeh E. F., Diskin S. J., Laudenslager M., Winter C., Cole K. A., Glessner J. T., Kim C., Frackelton E. C., Casalunovo T., Eckert A. W., Capasso M., Rappaport E. F., McConville C., London W. B., Seeger R. C., Rahman N., Devoto M., Grant S. F.A., Li H., Hakonarson H.
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N Engl J Med 2008;
published at www.nejm.org on
May 7, 2008
(10.1056/NEJMoa0708698).
Original Articles
Neuroblastoma — Linking a Common Allele to a Rare Disease
Kushner B. H., Cheung N.-K. V.
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N Engl J Med 2008;
published at www.nejm.org on
May 7, 2008
(10.1056/NEJMe0802701).
Editorials
Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults
Morita H., Rehm H. L., Menesses A., McDonough B., Roberts A. E., Kucherlapati R., Towbin J. A., Seidman J.G., Seidman C. E.
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N Engl J Med 2008;
358:1899-1908, May 1, 2008;
published at www.nejm.org on Apr 9, 2008 (10.1056/NEJMoa075463).
Original Articles
Mutations and Treatment Outcome in Cytogenetically Normal Acute Myeloid Leukemia
Schlenk R. F., Döhner K., Krauter J., Fröhling S., Corbacioglu A., Bullinger L., Habdank M., Späth D., Morgan M., Benner A., Schlegelberger B., Heil G., Ganser A., Döhner H., the German–Austrian Acute Myeloid Leukemia Study Group
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N Engl J Med 2008;
358:1909-1918, May 1, 2008.
Original Articles
MicroRNA Expression in Cytogenetically Normal Acute Myeloid Leukemia
Marcucci G., Radmacher M. D., Maharry K., Mrózek K., Ruppert A. S., Paschka P., Vukosavljevic T., Whitman S. P., Baldus C. D., Langer C., Liu C.-G., Carroll A. J., Powell B. L., Garzon R., Croce C. M., Kolitz J. E., Caligiuri M. A., Larson R. A., Bloomfield C. D.
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N Engl J Med 2008;
358:1919-1928, May 1, 2008.
Original Articles
Diagnosis and Prognosis in Acute Myeloid Leukemia — The Art of Distinction
Löwenberg B.
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N Engl J Med 2008;
358:1960-1962, May 1, 2008.
Editorials
Multiple Genetic Loci for Bone Mineral Density and Fractures
Styrkarsdottir U., Halldorsson B. V., Gretarsdottir S., Gudbjartsson D. F., Walters G. B., Ingvarsson T., Jonsdottir T., Saemundsdottir J., Center J. R., Nguyen T. V., Bagger Y., Gulcher J. R., Eisman J. A., Christiansen C., Sigurdsson G., Kong A., Thorsteinsdottir U., Stefansson K.
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N Engl J Med 2008;
published at www.nejm.org on
Apr 29, 2008
(10.1056/NEJMoa0801197).
Original Articles
Bona Fide Genetic Associations with Bone Mineral Density
Hirschhorn J. N., Gennari L.
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N Engl J Med 2008;
published at www.nejm.org on
Apr 29, 2008
(10.1056/NEJMe0803046).
Editorials
Brief Report:Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis
Maguire A. M., Simonelli F., Pierce E. A., Pugh E. N. Jr., Mingozzi F., Bennicelli J., Banfi S., Marshall K. A., Testa F., Surace E. M., Rossi S., Lyubarsky A., Arruda V. R., Konkle B., Stone E., Sun J., Jacobs J., Dell'Osso L., Hertle R., Ma J.-x., Redmond T. M., Zhu X., Hauck B., Zelenaia O., Shindler K. S., Maguire M. G., Wright J. F., Volpe N. J., McDonnell J. W., Auricchio A., High K. A., Bennett J.
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N Engl J Med 2008;
published at www.nejm.org on
Apr 27, 2008
(10.1056/NEJMoa0802315).
Original Articles
Brief Report:Safety and Efficacy of Gene Transfer for Leber's Congenital Amaurosis
Maguire A. M., Simonelli F., Pierce E. A., Pugh E. N. Jr., Mingozzi F., Bennicelli J., Banfi S., Marshall K. A., Testa F., Surace E. M., Rossi S., Lyubarsky A., Arruda V. R., Konkle B., Stone E., Sun J., Jacobs J., Dell'Osso L., Hertle R., Ma J.-x., Redmond T. M., Zhu X., Hauck B., Zelenaia O., Shindler K. S., Maguire M. G., Wright J. F., Volpe N. J., McDonnell J. W., Auricchio A., High K. A., Bennett J.
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N Engl J Med 2008;
published at www.nejm.org on
Apr 27, 2008
(10.1056/NEJMoa0802315).
Original Articles
Brief Report:Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis
Bainbridge J. W.B., Smith A. J., Barker S. S., Robbie S., Henderson R., Balaggan K., Viswanathan A., Holder G. E., Stockman A., Tyler N., Petersen-Jones S., Bhattacharya S. S., Thrasher A. J., Fitzke F. W., Carter B. J., Rubin G. S., Moore A. T., Ali R. R.
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N Engl J Med 2008;
published at www.nejm.org on
Apr 27, 2008
(10.1056/NEJMoa0802268).
Original Articles
Preliminary Results of Gene Therapy for Retinal Degeneration
Miller J. W.
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N Engl J Med 2008;
published at www.nejm.org on
Apr 27, 2008
(10.1056/NEJMe0803081).
Editorials
Brief Report:Pyruvate Kinase Deficiency and Malaria
Ayi K., Min-Oo G., Serghides L., Crockett M., Kirby-Allen M., Quirt I., Gros P., Kain K. C.
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N Engl J Med 2008;
358:1805-1810, Apr 24, 2008;
published at www.nejm.org on Apr 16, 2008 (10.1056/NEJMoa072464).
Original Articles
Brief Report:Mutations in the Iodotyrosine Deiodinase Gene and Hypothyroidism
Moreno J. C., Klootwijk W., van Toor H., Pinto G., D'Alessandro M., Lèger A., Goudie D., Polak M., Grüters A., Visser T. J.
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N Engl J Med 2008;
358:1811-1818, Apr 24, 2008.
Original Articles
A Malaria Fingerprint in the Human Genome?
Daily J. P., Sabeti P.
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N Engl J Med 2008;
358:1855-1856, Apr 24, 2008;
published at www.nejm.org on Apr 16, 2008 (10.1056/NEJMe0801414).
Editorials
Reduce, Recycle, Reuse — Iodotyrosine Deiodinase in Thyroid Iodide Metabolism
Kopp P. A.
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N Engl J Med 2008;
358:1856-1859, Apr 24, 2008.
Editorials
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