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1.
J Med Genet ; 60(7): 669-678, 2023 07.
Artigo em Inglês | MEDLINE | ID: mdl-36572524

RESUMO

OBJECTIVE: To describe national patterns of National Health Service (NHS) analysis of mismatch repair (MMR) genes in England using individual-level data submitted to the National Disease Registration Service (NDRS) by the NHS regional molecular genetics laboratories. DESIGN: Laboratories submitted individual-level patient data to NDRS against a prescribed data model, including (1) patient identifiers, (2) test episode data, (3) per-gene results and (4) detected sequence variants. Individualised per-laboratory algorithms were designed and applied in NDRS to extract and map the data to the common data model. Laboratory-level MMR activity audit data from the Clinical Molecular Genetics Society/Association of Clinical Genomic Science were used to assess early years' missing data. RESULTS: Individual-level data from patients undergoing NHS MMR germline genetic testing were submitted from all 13 English laboratories performing MMR analyses, comprising in total 16 722 patients (9649 full-gene, 7073 targeted), with the earliest submission from 2000. The NDRS dataset is estimated to comprise >60% of NHS MMR analyses performed since inception of NHS MMR analysis, with complete national data for full-gene analyses for 2016 onwards. Out of 9649 full-gene tests, 2724 had an abnormal result, approximately 70% of which were (likely) pathogenic. Data linkage to the National Cancer Registry demonstrated colorectal cancer was the most frequent cancer type in which full-gene analysis was performed. CONCLUSION: The NDRS MMR dataset is a unique national pan-laboratory amalgamation of individual-level clinical and genomic patient data with pseudonymised identifiers enabling linkage to other national datasets. This growing resource will enable longitudinal research and can form the basis of a live national genomic disease registry.


Assuntos
Neoplasias , Medicina Estatal , Humanos , Reparo de Erro de Pareamento de DNA/genética , Laboratórios , Genômica
2.
Am J Med Genet A ; 149A(10): 2147-51, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19764026

RESUMO

Von Hippel-Lindau (VHL) syndrome is a dominantly inherited familial cancer syndrome caused by mutations in the VHL gene. VHL syndrome displays marked variation in expression and analysis of genotype-phenotype correlations have led to the concept of four subtypes of VHL syndrome (Types 1, 2A-C). Type 2 subtypes of VHL syndrome are characterized by the presence of pheochromocytoma and the three Type 2 subtypes are associated with differing risks of hemangioblastoma and renal cell carcinoma (RCC). Type 2 VHL syndrome is usually associated with surface missense mutations. Type 1 VHL syndrome is most commonly caused by germline exon deletions and truncating mutations and is characterized by susceptibility to hemangioblastomas and RCC but not pheochromocytoma. Recently, it has been suggested that large VHL gene deletions involving C3orf10 (HSPC300) might be associated with a low risk of RCC. We have reviewed the molecular and clinical characteristics of 127 individuals with germline VHL gene deletions. Large VHL gene deletions associated with a contiguous loss of C3orf10 were associated with a significantly lower lifetime risk of RCC than deletions that did not involve C3orf10. The risks of hemangioblastomas were similar in both groups. These results add to the growing body of evidence suggesting that patients with VHL syndrome caused by large VHL deletions that include C3orf10 may be designated as having a specific subtype (Type 1B) of the disorder.


Assuntos
Deleção de Genes , Fenótipo , Proteína Supressora de Tumor Von Hippel-Lindau/genética , Doença de von Hippel-Lindau/classificação , Neoplasias das Glândulas Suprarrenais/complicações , Neoplasias das Glândulas Suprarrenais/genética , Carcinoma de Células Renais/complicações , Carcinoma de Células Renais/genética , Neoplasias Cerebelares/complicações , Neoplasias Cerebelares/genética , Proteínas do Citoesqueleto/genética , Análise Mutacional de DNA , Éxons/genética , Proteína do Grupo de Complementação D2 da Anemia de Fanconi/genética , Genótipo , Mutação em Linhagem Germinativa , Hemangioblastoma/complicações , Hemangioblastoma/genética , Humanos , Neoplasias Renais/complicações , Neoplasias Renais/genética , Feocromocitoma/complicações , Feocromocitoma/genética , Neoplasias da Retina/complicações , Neoplasias da Retina/genética , Doença de von Hippel-Lindau/complicações , Doença de von Hippel-Lindau/genética
3.
Proc Natl Acad Sci U S A ; 105(12): 4775-80, 2008 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-18349145

RESUMO

It is well established that an increase in iron supply causes an increase in total oceanic primary production in many regions, but the physiological mechanism driving the observed increases has not been clearly identified. The Southern Ocean iron enrichment experiment, an iron fertilization experiment in the waters closest to Antarctica, resulted in a 9-fold increase in chlorophyll (Chl) concentration and a 5-fold increase in integrated primary production. Upon iron addition, the maximum quantum yield of photosynthesis (phi(m)) rapidly doubled, from 0.011 to 0.025 mol C.mol quanta(-1). Paradoxically, this increase in light-limited productivity was not accompanied by a significant increase in light-saturated productivity (P(max)(b)). P(max)(b), maximum Chl normalized productivity, was 1.34 mg C.mg Chl(-1).h(-1) outside and 1.49 mg C.mg Chl(-1).h(-1) inside the iron-enriched patch. The importance of phi(m) as compared with P(max)(b) in controlling the biological response to iron addition has vast implications for understanding the ecological response to iron. We show that an iron-driven increase in phi(m) is the proximate physiological mechanism affected by iron addition and can account for most of the increases in primary production. The relative importance of phi(m) over P(max)(b) in this iron-fertilized bloom highlights the limitations of often-used primary productivity algorithms that are driven by estimates of P(max)(b) but largely ignore variability in phi(m) and light-limited productivity. To use primary productivity models that include variability in iron supply in prediction or forecasting, the variability of light-limited productivity must be resolved.


Assuntos
Ferro/farmacologia , Fotossíntese , Fitoplâncton/efeitos dos fármacos , Fitoplâncton/fisiologia , Análise de Variância , Carotenoides/metabolismo , Fracionamento Químico , Clorofila/metabolismo , Modelos Biológicos , Oceanos e Mares , Fotossíntese/efeitos dos fármacos , Fatores de Tempo
4.
Science ; 304(5669): 408-14, 2004 Apr 16.
Artigo em Inglês | MEDLINE | ID: mdl-15087542

RESUMO

The availability of iron is known to exert a controlling influence on biological productivity in surface waters over large areas of the ocean and may have been an important factor in the variation of the concentration of atmospheric carbon dioxide over glacial cycles. The effect of iron in the Southern Ocean is particularly important because of its large area and abundant nitrate, yet iron-enhanced growth of phytoplankton may be differentially expressed between waters with high silicic acid in the south and low silicic acid in the north, where diatom growth may be limited by both silicic acid and iron. Two mesoscale experiments, designed to investigate the effects of iron enrichment in regions with high and low concentrations of silicic acid, were performed in the Southern Ocean. These experiments demonstrate iron's pivotal role in controlling carbon uptake and regulating atmospheric partial pressure of carbon dioxide.


Assuntos
Carbono/metabolismo , Ferro , Fitoplâncton/crescimento & desenvolvimento , Ácido Silícico , Atmosfera , Biomassa , Carbono/análise , Dióxido de Carbono/análise , Dióxido de Carbono/metabolismo , Clorofila/análise , Clorofila A , Diatomáceas/crescimento & desenvolvimento , Diatomáceas/metabolismo , Ecossistema , Ferro/análise , Ferro/metabolismo , Nitratos/análise , Nitratos/metabolismo , Nitrogênio/análise , Nitrogênio/metabolismo , Oceanos e Mares , Fotossíntese , Fitoplâncton/metabolismo , Água do Mar/química , Ácido Silícico/análise , Ácido Silícico/metabolismo
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