Search Results - "Green, P.M."

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    The Northern Oscillation Index (NOI): a new climate index for the northeast Pacific by Schwing, F.B, Murphree, T, Green, P.M

    Published in Progress in oceanography (01-01-2002)
    “…We introduce the Northern Oscillation Index (NOI), a new index of climate variability based on the difference in sea level pressure (SLP) anomalies at the…”
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    The evolution of oceanic and atmospheric anomalies in the northeast Pacific during the El Niño and La Niña events of 1995–2001 by Schwing, F.B., Murphree, T., deWitt, L., Green, P.M.

    Published in Progress in oceanography (01-01-2002)
    “…From late 1995 through early 2001, three major interannual climate events occurred in the tropical Pacific; the 1995-97 La Nina (LN), 1997-98 el Nino (EN), and…”
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    Int22h‐related inversions causing hemophilia A: a novel insight into their origin and a new more discriminant PCR test for their detection by BAGNALL, R. D., GIANNELLI, F., GREEN, P. M.

    Published in Journal of thrombosis and haemostasis (01-03-2006)
    “…Background: Intrachromosomal, homologous recombination of the duplicon int22h‐1 with int22h‐2 or int22h‐3 causes inversions accounting for 45% of severe…”
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    Developing a Student—Focused Undergraduate Laboratory by Heath, W. P., Onel, O., Green, P. M., Lennox, B., Gai, Zhenyu, He, Zhiwei, Liñan, M. C. Rodriguez

    “…Laboratories are an essential component of our undergraduate curricula in the School of Electrical and Electronic Engineering at the University of Manchester…”
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    Mutation Rates in Humans. II. Sporadic Mutation-Specific Rates and Rate of Detrimental Human Mutations Inferred from Hemophilia B by Giannelli, F., Anagnostopoulos, T., Green, P.M.

    Published in American journal of human genetics (01-12-1999)
    “…We estimated the rates per base per generation of specific types of mutations, using our direct estimate of the overall mutation rate for hemophilia B and…”
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    Mutation Rates in Humans. I. Overall and Sex-Specific Rates Obtained from a Population Study of Hemophilia B by Green, P.M., Saad, S., Lewis, C.M., Giannelli, F.

    Published in American journal of human genetics (01-12-1999)
    “…A population-based study of hemophilia B mutations was conducted in the United Kingdom in order to construct a national confidential database of mutations and…”
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    Synthetic Strategy Towards Heterodimetallic Half-Sandwich Complexes Based on a Symmetric Ditopic Ligand by Green, Lewis P M, Steel, Tasha R, Riisom, Mie, Hanif, Muhammad, Söhnel, Tilo, Jamieson, Stephen M F, Wright, L James, Crowley, James D, Hartinger, Christian G

    Published in Frontiers in chemistry (03-12-2021)
    “…Multimetallic complexes have been shown in several examples to possess greater anticancer activity than their monometallic counterparts. The increased activity…”
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    Ultrarapid mutation detection by multiplex, solid-phase chemical cleavage by ROWLEY, G, SAAD, S, GIANNELLI, F, GREEN, P. M

    Published in Genomics (San Diego, Calif.) (10-12-1995)
    “…The chemical cleavage of mismatches in heteroduplexes formed by probe and test DNA detects and locates any sequence change in long DNA segments (approximately…”
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    DNA variation in a 13‐Mb region including the F9 gene: inferring the genealogical history and causal role of a hemophilia B mutation (IVS 5+13 A→G) by Anagnostopoulos, T., Morris, A. P., Ayres, K. L., Giannelli, F., Green, P. M.

    Published in Journal of thrombosis and haemostasis (01-12-2003)
    “…About 5.5% of all UK hemophilia B patients have the base substitution IVS 5+13 A→G as the only change in their factor (F)IX gene (F9). This generates a novel…”
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    Sequence, exon-intron organization, transcription and mutational analysis of prnA, the gene encoding the transcriptional activator of the prn gene cluster in Aspergillus nidulans by Cazelle, B, Pokorska, A, Hull, E, Green, P.M, Stanway, G, Scazzocchio, C

    Published in Molecular microbiology (01-04-1998)
    “…The prnA gene codes for a transcriptional activator that mediates proline induction of four other genes involved in proline utilization as a nitrogen and/or…”
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    Direct detection of point mutations by mismatch analysis: application to haemophilia B by MONTANDON, A. J, GREEN, P. M, GIANNELLI, F, BENTLEY, D. R

    Published in Nucleic acids research (11-05-1989)
    “…Rapid detection of point mutations in genomic DNA has been achieved by chemical mismatch analysis of heteroduplexes formed between amplified wild-type and…”
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    Factor VIII gene explains all cases of haemophilia A by Naylor, J A, Green, P M, Rizza, C R, Giannelli, F

    Published in The Lancet (British edition) (31-10-1992)
    “…Using an mRNA-based method to examine haemophilia A mutations we provide an explanation for the puzzling report that half of the mutations causing severe…”
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    Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994 by Giannelli, F., Green, P.M., Sommer, S.S., Lillicrap, D.P., Ludwig, M., Schwaab, R., Reitsma, P.H., Goossens, M., Yoshioka, A., Brownlee, G.G.

    Published in Nucleic acids research (01-09-1994)
    “…The fifth edition of the haemophilia B database lists in easily accessible form all known factor IX mutations due to small changes (base substitutions and…”
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    Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene by Naylor, J A, Green, P M, Montandon, A J, Rizza, C R, Giannelli, F

    Published in The Lancet (British edition) (16-03-1991)
    “…In an attempt to replace the existing, DNA-based, 50% effective, carrier and prenatal diagnoses of haemophilia A with the 100% successful direct detection of…”
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    Idiopathic intracranial haemorrhage in the fetus by Green, P M, Wilson, H, Romaniuk, C, May, P, Welch, C R

    Published in Fetal diagnosis and therapy (01-09-1999)
    “…Intracranial haemorrhage in the fetus has been reported with associated mortality and morbidity. This case report describes idiopathic subdural haematomas…”
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