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Serveur d'exploration sur le lymphœdème - Analysis (UK)

Index « Auteurs » - entrée « Alberto Smith »
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Alberto De Barros Lopes < Alberto Smith < Albis-Francesco Gabrielli  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
000053 (2017) Merlijn J. Meens [Suisse] ; Issa Kutkut [Suisse] ; Viviane Rochemont [Suisse] ; Juan Dubrot [Suisse] ; Fouad R. Kaladji [Suisse] ; Amélie Sabine [Suisse] ; Oliver Lyons [Royaume-Uni] ; Stefanie Hendrikx [Suisse] ; Jeremiah Bernier-Latmani [Suisse] ; Friedemann Kiefer [Allemagne] ; Alberto Smith [Royaume-Uni] ; Stéphanie Hugues [Suisse] ; Tatiana V. Petrova [Suisse] ; Brenda R. Kwak [Suisse]Cx47 fine-tunes the handling of serum lipids but is dispensable for lymphatic vascular function
000621 (2011) Russell H. Mellor [Royaume-Uni] ; Naomi Tate ; Anthony W B. Stanton ; Charlotte Hubert ; Taija M Kinen ; Alberto Smith ; Kevin G. Burnand ; Steve Jeffery ; J Rodney Levick ; Peter S. MortimerMutations in FOXC2 in humans (lymphoedema distichiasis syndrome) cause lymphatic dysfunction on dependency.
000624 (2011) Samuel Ogunbiyi [Royaume-Uni] ; Ganessen Chinien ; Della Field ; Julia Humphries ; Kevin Burand ; Barbara Sawyer ; Steve Jeffrey ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve Clasper ; Dave Jackson ; Alberto SmithMolecular characterization of dermal lymphatic endothelial cells from primary lymphedema skin.
000633 (2011) Eleni Bazigou [Royaume-Uni] ; Oliver T. A. Lyons [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Graham E. Venn [Royaume-Uni] ; Celia Cope [Royaume-Uni] ; Nigel A. Brown [Royaume-Uni] ; Taija Makinen [Royaume-Uni]Genes regulating lymphangiogenesis control venous valve formation and maintenance in mice
000701 (2011) Russell H. Mellor [Royaume-Uni] ; Naomi Tate [Royaume-Uni] ; Anthony W. B. Stanton [Royaume-Uni] ; Charlotte Hubert [Royaume-Uni] ; Taija M Kinen [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Kevin G. Burnand [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; J. Rodney Levick [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]Mutations in FOXC2 in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency
000769 (2010) Russell H. Mellor [Royaume-Uni] ; Charlotte E. Hubert [Royaume-Uni] ; Anthony W. B. Stanton [Royaume-Uni] ; Naomi Tate [Royaume-Uni] ; Victoria Akhras [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Kevin G. Burnand [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; Taija M Kinen [Royaume-Uni] ; J. Rodney Levick [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]Lymphatic Dysfunction, Not Aplasia, Underlies Milroy Disease
000969 (2007) Russell H. Mellor [Royaume-Uni] ; Glen Brice ; Anthony W B. Stanton ; Jane French ; Alberto Smith ; Steve Jeffery ; J Rodney Levick ; Kevin G. Burnand ; Peter S. MortimerMutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb.
000A37 (2007) Russell H. Mellor [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Anthony W. B. Stanton [Royaume-Uni] ; Jane French [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] ; J. Rodney Levick [Royaume-Uni] ; Kevin G. Burnand [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni]Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb
000B76 (2005) Carolyn Sholto-Douglas-Vernon [Royaume-Uni] ; Rachel Bell [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Mansoor Sarfarazi [États-Unis] ; Anne H. Child [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Russell Mellor [Royaume-Uni] ; Kevin Burnand [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve Jeffery [Royaume-Uni]Lymphoedema-distichiasis and FOXC2 : unreported mutations, de novo mutation estimate, families without coding mutations

List of associated KwdEn.i

Nombre de
documents		Descripteur
5Female
5Humans
5Lymphedema (genetics)
5Male
4Adult
4Middle Aged
4Mutation
3Aged
3Lymphedema
3Lymphedema (pathology)
2Distichiasis
2Foot
2Forearm
2Forkhead Transcription Factors (genetics)
2Human
2Lymphatic System (pathology)
2Lymphedema (diagnostic imaging)
2Lymphedema (physiopathology)
2Ultrasonography, Doppler, Color
2Young Adult
1Amino Acid Sequence
1Biopsy
1Cardiovascular disease
1Case-Control Studies
1Cell Proliferation (drug effects)
1Cells, Cultured
1Chromosomes, Human, Pair 16 (genetics)
1Circulatory system
1DNA-Binding Proteins (genetics)
1De novo
1Dextrans
1Dysfunction
1Endothelial Cells (cytology)
1Endothelial Cells (metabolism)
1Endothelial Cells (pathology)
1Eyelashes (abnormalities)
1Eyelashes (diagnostic imaging)
1Eyelashes (pathology)
1Family
1Fluorescein-5-isothiocyanate (analogs & derivatives)
1Fluorescence
1Fluorescent Dyes
1Forkhead Transcription Factors
1Gene Expression Profiling
1Gene Expression Regulation
1Gene Frequency
1Genes, Dominant
1Genetic Linkage
1Genetics
1Germ-Line Mutation
1Gravitation
1Immunohistochemistry
1Leg (blood supply)
1Leg (diagnostic imaging)
1Lower limb
1Lymphatic
1Lymphatic Abnormalities (diagnostic imaging)
1Lymphatic Abnormalities (genetics)
1Lymphatic Abnormalities (physiopathology)
1Lymphatic System (diagnostic imaging)
1Lymphatic System (physiology)
1Lymphatic System (physiopathology)
1Lymphatic Vessels (diagnostic imaging)
1Lymphatic Vessels (embryology)
1Lymphatic Vessels (pathology)
1Lymphedema (congenital)
1Lymphedema (etiology)
1Lymphedema (metabolism)
1Lymphography
1Lymphography (methods)
1Mammalia
1Microlymphography
1Molecular Sequence Data
1Mutagenesis, Insertional
1Mutation, Missense
1Open Reading Frames (genetics)
1Pedigree
1Saphenous Vein (diagnostic imaging)
1Saphenous Vein (physiopathology)
1Sequence Deletion (genetics)
1Skin
1Skin (cytology)
1Skin (metabolism)
1Skin (pathology)
1Stress, Physiological
1Transcription Factors (genetics)
1United Kingdom
1Varicose Veins (diagnostic imaging)
1Varicose Veins (genetics)
1Varicose Veins (physiopathology)
1Vascular Endothelial Growth Factor Receptor-3 (genetics)
1Vascular Endothelial Growth Factors (pharmacology)
1Vein valve
1Veins (embryology)
1Vesicular Transport Proteins (metabolism)

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