Search Results - "Green, P.M."
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The Northern Oscillation Index (NOI): a new climate index for the northeast Pacific
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
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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3
Polymorphism and hemophilia A causing inversions in distal Xq28: a complex picture
Published in Journal of thrombosis and haemostasis (01-11-2005)Get full text
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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
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
Published in International journal of electrical engineering & education (01-07-2013)“…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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Unusual expression of the F9 gene in peripheral lymphocytes hinders investigation of F9 mRNA in hemophilia B patients
Published in Journal of thrombosis and haemostasis (01-12-2003)Get full text
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Mutation Rates in Humans. II. Sporadic Mutation-Specific Rates and Rate of Detrimental Human Mutations Inferred from Hemophilia B
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
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
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
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)
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
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
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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14
Factor VIII gene explains all cases of haemophilia A
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
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
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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Haemophilia B: database of point mutations and short additions and deletions—fourth edition, 1993
Published in Nucleic acids research (01-07-1993)Get full text
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Idiopathic intracranial haemorrhage in the fetus
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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A Genetic View on the Etiology of the Inhibitor Complication
Published in Blood (15-03-1996)Get full text
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Dmitriev, Sviatoslav. The birth of the Athenian community: from Solon to Cleisthenes
Published in CHOICE: Current Reviews for Academic Libraries (01-09-2018)Get full text
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