Genetic Markers < Genetic Predisposition to Disease < Genetic Research

Facettes : AffPays.f Mesh.f AffRegion.f AffVille.f

List of bibliographic references

Number of relevant bibliographic references: 56.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000298 (2000)	A J Terhell [Pays-Bas] ; J J Houwing-Duistermaat ; Y. Ruiterman ; M. Haarbrink ; K. Abadi ; M. Yazdanbakhsh	Clustering of Brugia malayi infection in a community in South-Sulawesi, Indonesia.
000337 (2000)	S C Robertson [États-Unis] ; J A Tynan ; D J Donoghue	RTK mutations and human syndromeswhen good receptors turn bad.
000661 (2001)	S. Aradhya [États-Unis] ; D L Nelson	NF-kappaB signaling and human disease.
000746 (2001)	E H Choi [États-Unis] ; P A Zimmerman ; C B Foster ; S. Zhu ; V. Kumaraswami ; T B Nutman ; S J Chanock	Genetic polymorphisms in molecules of innate immunity and susceptibility to infection with Wuchereria bancrofti in South India.
000D66 (2003)	Eun Hwa Choi [États-Unis] ; Thomas B. Nutman ; Stephen J. Chanock	Genetic variation in immune function and susceptibility to human filariasis.
001715 (2003)	A G Hise [États-Unis] ; F E Hazlett ; M J Bockarie ; P A Zimmerman ; D J Tisch ; J W Kazura	Polymorphisms of innate immunity genes and susceptibility to lymphatic filariasis.
001957 (2004)	H R Dürr [Allemagne] ; C. Pellengahr ; A. Nerlich ; A. Baur ; M. Maier ; V. Jansson	Stewart-Treves syndrome as a rare complication of a hereditary lymphedema.
002033 (2005)	J H Williams [Afrique du Sud]	Lymphangiosarcoma of dogs: a review.
002354 (2007)	Amy E. Young [États-Unis] ; Leslie P. Bower ; Verena K. Affolter ; Hilde E V. De Cock ; Gregory L. Ferraro ; Danika L. Bannasch	Evaluation of FOXC2 as a candidate gene for chronic progressive lymphedema in draft horses.
002399 (2006)	A. Ghalamkarpour [Belgique] ; S. Morlot ; A. Raas-Rothschild ; A. Utkus ; J B Mulliken ; L M Boon ; M. Vikkula	Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations.
002572 (2007)	Mylène Béri-Deixheimer [France] ; Marie-José Gregoire ; Annick Toutain ; Karène Brochet ; Sylvain Briault ; Jean-Luc Schaff ; Bruno Leheup ; Philippe Jonveaux	Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'.
002B19 (2008)	Sajid Malik [Allemagne] ; Karl-Heinz Grzeschik	Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.
003083 (2008)	R J Damstra [Pays-Bas] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]	Diagnosis and therapy in children with lymphoedema.
003113 (2008)	John G. West [États-Unis] ; Jeffrey N. Weitzel ; May Lin Tao ; Michele Carpenter ; Justin E. West ; Caitlin Fanning	BRCA mutations and the risk of angiosarcoma after breast cancer treatment.
003573 (2009)	Fasil Tekola [Éthiopie, Royaume-Uni, États-Unis] ; Susan Bull [Royaume-Uni] ; Bobbie Farsides [Royaume-Uni] ; Melanie J. Newport [Royaume-Uni] ; Adebowale Adeyemo [États-Unis] ; Charles N. Rotimi [États-Unis] ; Gail Davey [Éthiopie]	Impact of social stigma on the process of obtaining informed consent for genetic research on podoconiosis: a qualitative study
003616 (2009)	Karen T. Cuenco [États-Unis] ; Eric A. Ottesen ; Steven A. Williams ; Thomas B. Nutman ; Cathy Steel	Heritable factors play a major role in determining host responses to Wuchereria bancrofti infection in an isolated South Pacific island population.
003727 (2010)	Fiona Connell [Royaume-Uni] ; Kamini Kalidas ; Pia Ostergaard ; Glen Brice ; Tessa Homfray ; Lesley Roberts ; David J. Bunyan ; Sally Mitton ; Sahar Mansour ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve Jeffery	Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.
004295 (2011)	Zulkarnain Md Idris [Malaisie] ; Noorizan Miswan ; Jamail Muhi ; Tajul Ariffin Awang Mohd ; Jürgen F J. Kun ; Rahmah Noordin	Association of CTLA4 gene polymorphisms with lymphatic filariasis in an East Malaysian population.
004426 (2011)	Aditya Kumar Panda [Inde] ; Prakash Kumar Sahoo ; Anna Solami Kerketta ; Santanu Kumar Kar ; Balachandran Ravindran ; Ashok Kumar Satapathy	Human lymphatic filariasis: genetic polymorphism of endothelin-1 and tumor necrosis factor receptor II correlates with development of chronic disease.
004604 (2011)	Alexander Yaw Debrah [Ghana] ; Linda Batsa ; Anna Albers ; Sabine Mand ; Mohammad Reza Toliat ; Peter Nürnberg ; Ohene Adjei ; Achim Hoerauf ; Kenneth Pfarr	Transforming growth factor-β1 variant Leu10Pro is associated with both lack of microfilariae and differential microfilarial loads in the blood of persons infected with lymphatic filariasis.
004641 (2011)	Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson ; Fiona C. Connell ; Colin G. Steward ; Glen Brice ; Wesley J. Woollard ; Dimitra Dafou ; Tatjana Kilo ; Sarah Smithson ; Peter Lunt ; Victoria A. Murday ; Shirley Hodgson ; Russell Keenan ; Daniela T. Pilz ; Ines Martinez-Corral ; Taija Makinen ; Peter S. Mortimer ; Steve Jeffery ; Richard C. Trembath ; Sahar Mansour	Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).

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