Kinetics and mechanism of reactions of water-soluble ferriporphyrins. 2. Reduction by ascorbic acid
In: Inorganic chemistry. - Washington, DC : American Chemical Society, ISSN 1520-510X, Vol. 17, No. 1 (1978), p. 74-77 Zugang:
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Kinetics and mechanism of reactions of water-soluble ferriporphyrins. 1. Monomer-dimer interactions
In: Inorganic chemistry. - Washington, DC : American Chemical Society, ISSN 1520-510X, Vol. 17, No. 1 (1978), p. 71-73 Zugang:
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Temperature dependence of the inhomogeneous line broadening in the EPR spectra of doxyl-labeled alkyl chains
In: The journal of physical chemistry . - Washington, DC : American Chemical Society, Vol. 91, No. 7 (1987), p. 1701-1702 Zugang:
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Stepwise sequence determination from the carboxyl terminus of peptides
In: Biochemistry. - Columbus, Ohio : American Chemical Society, ISSN 1520-4995, Vol. 21, No. 16 (1982), p. 3750-3757 Zugang:
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Deamination of 2-phenyl-2-(2-methoxyphenyl)ethylamine
In: The journal of organic chemistry. - [S.l.] : American Chemical Society, ISSN 1520-6904, Vol. 42, No. 20 (1977), p. 3306-3307 Zugang:
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Semipinacol rearrangements involving trifluoromethylphenyl groups
In: The journal of organic chemistry. - [S.l.] : American Chemical Society, ISSN 1520-6904, Vol. 42, No. 5 (1977), p. 868-871 Zugang:
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Semipinacolic deamination of 2-amino-1-(2-methoxyphenyl)-1-phenylethanol
In: The journal of organic chemistry. - [S.l.] : American Chemical Society, ISSN 1520-6904, Vol. 37, No. 15 (1972), p. 2494-2497 Zugang:
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Sapphyrins: novel aromatic pentapyrrolic macrocycles
In: American Chemical Society: Journal of the American Chemical Society. - Washington, DC : American Chemical Society, ISSN 1520-5126, Vol. 105, No. 21 (1983), p. 6429-6436 Zugang:
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Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 345, No. 6277 (1990), p. 736-739 Zugang:
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1990
HEREDITARY spherocytosis (HS) is one of the most common hereditary haemolytic anaemias1. HS red cells from both autosound dominant and recessive variants are spectrin-deficient2,3, which correlates with the severity of the disease3. Some patients with recessive HS have a mutation in the... mehr
New models of collaboration in genome-wide association studies: the Genetic Association Information Network
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 9 (2007), p. 1045-1051 Zugang:
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2007
The Genetic Association Information Network (GAIN) is a public-private partnership established to investigate the genetic basis of common diseases through a series of collaborative genome-wide association studies. GAIN has used new approaches for project selection, data deposition and... mehr
Lung cancer: Intragenic ERBB2 kinase mutations in tumours
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 431, No. 7008 (2004), p. 525-526 Zugang:
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2004
The protein-kinase family is the most frequently mutated gene family found in human cancer and faulty kinase enzymes are being investigated as promising targets for the design of antitumour therapies. We have sequenced the gene encoding the transmembrane protein tyrosine kinase ERBB2 (also known... mehr
Initial sequencing and analysis of the human genome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 409, No. 6822 (2001), p. 860-921 Zugang:
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2001
The human genome holds an extraordinary trove of information about human development, physiology, medicine and evolution. Here we report the results of an international collaboration to produce and make freely available a draft sequence of the human genome. We also present an initial analysis of... mehr
Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 432, No. 7018 (2004), p. 695-716 Zugang:
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2004
We present here a draft genome sequence of the red jungle fowl, Gallus gallus. Because the chicken is a modern descendant of the dinosaurs and the first non-mammalian amniote to have its genome sequenced, the draft sequence of its genome—composed of approximately one billion base pairs of... mehr