Forkhead Box Protein O3 < Forkhead Transcription Factors < Formaldehyde

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

List of bibliographic references

Number of relevant bibliographic references: 77.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000486 (2000)	Jianming Fang ; Susan L. Dagenais ; Robert P. Erickson ; Martin F. Arlt ; Michael W. Glynn ; Jerome L. Gorski ; Laurie H. Seaver [États-Unis] ; Thomas W. Glover	Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome
000599 (2001)	L R Osborne	'Forkhead' gene expression balanced on a knife-edge.
000621 (2001)	R P Erickson	Lymphedema-distichiasis and FOXC2 gene mutations.
000659 (2001)	D N Finegold [États-Unis] ; M A Kimak ; E C Lawrence ; K L Levinson ; E M Cherniske ; B R Pober ; J W Dunlap ; R E Ferrell	Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
000683 (2001)	M J Karkkainen [Finlande] ; L. Jussila ; R E Ferrell ; D N Finegold ; Kari Alitalo [Finlande]	Molecular regulation of lymphangiogenesis and targets for tissue oedema.
000731 (2001)	R. Bell [Royaume-Uni] ; G. Brice ; A H Child ; V A Murday ; S. Mansour ; C J Sandy ; J R Collin ; A F Brady ; D F Callen ; K. Burnand ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Jeffery	Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene.
000799 (2001)	R. Erickson ; S. Dagenais ; M. Caulder ; C. Downs ; G. Herman ; M. Jones ; W. Kerstjens-Frederi. ; A. Lidral ; M. Mcdonald ; C. Nelson ; M. Witte ; T. Glover	Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations
000946 (2002)	Marika J. Karkkainen [Finlande] ; Kari Alitalo [Finlande]	Lymphatic endothelial regulation, lymphoedema, and lymph node metastasis.
000A31 (2002)	G. Brice ; S. Mansour ; R. Bell ; J. Collin ; A. Child ; A. Brady ; M. Sarfarazi ; K. Burnand ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; V. Murday	Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
000B32 (2002)	Elias I. Traboulsi [États-Unis] ; Khouloud Al-Khayer ; Masayuki Matsumoto ; Mark A. Kimak ; Susan Crowe ; Steven E. Wilson ; David N. Finegold ; Robert E. Ferrell ; David M. Meisler	Lymphedema-distichiasis syndrome and FOXC2 gene mutation.
000B81 (2002)	M. Bahuau [France] ; C. Houdayer ; M. Tredano ; V. Soupre ; R. Couderc ; M-P Vazquez	FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate.
000C07 (2002)	Robert E. Ferrell [États-Unis]	Research perspectives in inherited lymphatic disease.
000C23 (????)	Glen Brice	Diagnostic difficulties in lymphedema distichiasis.
000D44 (2003)	Benjamin M. Kriederman [États-Unis] ; Teressa L. Myloyde ; Marlys H. Witte ; Susan L. Dagenais ; Charles L. Witte ; Margaret Rennels ; Michael J. Bernas ; Michelle T. Lynch ; Robert P. Erickson ; Mark S. Caulder ; Naoyuki Miura ; David Jackson ; Brian P. Brooks ; Thomas W. Glover	FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
000D95 (2003)	Kara L. Levinson [États-Unis] ; Eleanor Feingold ; Robert E. Ferrell ; Thomas W. Glover ; Elias I. Traboulsi ; David N. Finegold	Age of onset in hereditary lymphedema.
000E90 (2003)	H. Kim [Canada] ; D J Dumont	Molecular mechanisms in lymphangiogenesis: model systems and implications in human disease.
001725 (2003)	Brian P. Brooks [États-Unis] ; Susan L. Dagenais ; Christine C. Nelson ; Michael W. Glynn ; Mark S. Caulder ; Catherine A. Downs ; Thomas W. Glover	Mutation of the FOXC2 gene in familial distichiasis.
001B00 (2004)	Tatiana V. Petrova [Finlande] ; Terhi Karpanen ; Camilla Norrmén ; Russell Mellor ; Tomoki Tamakoshi ; David Finegold ; Robert Ferrell ; Dontscho Kerjaschki ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Seppo Yl Herttuala ; Naoyuki Miura ; Kari Alitalo [Finlande]	Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis.
001B72 (2004)	Susan L. Dagenais [États-Unis] ; Rebecca L. Hartsough ; Robert P. Erickson ; Marlys H. Witte ; Matthew G. Butler ; Thomas W. Glover	Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.
001C00 (2004)	Cagri Yildirim-Toruner [États-Unis] ; Kavitha Subramanian ; Lamya El Manjra ; Emily Chen ; Stanley Goldstein ; Emilia Vitale	A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus.
001C49 (2004)	Naoyuki Miura [Japon]	[Multiple roles of forkhead genes in development and metabolism].

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