List of bibliographic references indexed by Transcription Factors (genetics)
Number of relevant bibliographic references: 30.
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20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 000805 (2017) |
Heinrich Schlums [Suède] ; Moonjung Jung [États-Unis] ; Hongya Han [Suède] ; Jakob Theorell [Suède] ; Venetia Bigley [Royaume-Uni] ; Samuel C C. Chiang [Suède] ; David S J. Allan [États-Unis] ; Jan K. Davidson-Moncada [États-Unis] ; Rachel E. Dickinson [Royaume-Uni] ; Tim D. Holmes [Suède] ; Amy P. Hsu [États-Unis] ; Danielle Townsley [États-Unis] ; Thomas Winkler [États-Unis] ; Weixin Wang ; P L Aukrust [Norvège] ; Ingvild Nord Y [Norvège] ; Katherine R. Calvo ; Steve M. Holland [États-Unis] ; Matthew Collin [Royaume-Uni] ; Cynthia E. Dunbar [États-Unis] ; Yenan T. Bryceson [Suède] | Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells. |
| 004645 (2012) |
Antoine Italiano [États-Unis, France] ; Rachael Thomas [États-Unis] ; Matthew Breen [États-Unis] ; Lei Zhang [États-Unis] ; Aimee M. Crago [États-Unis] ; Samuel Singer [États-Unis] ; Raya Khanin [États-Unis] ; Robert G. Maki [États-Unis] ; Aleksandra Mihailovic [États-Unis] ; Markus Hafner [États-Unis] ; Tom Tuschl [États-Unis] ; Cristina R. Antonescu [États-Unis] | The miR‐17‐92 cluster and its target THBS1 are differentially expressed in angiosarcomas dependent on MYC amplification |
| 006D68 (2008) |
Fiona Connell ; Glen Brice ; Peter Mortimer (dermatologue) [Royaume-Uni] | Phenotypic Characterization of Primary Lymphedema |
| 007571 (2007) |
M. A. M. Van Steensel [Pays-Bas] ; M. Van Geel [Pays-Bas] ; C. Schrander-Stumpel [Pays-Bas] ; P. M. Steijlen [Pays-Bas] ; J. C. J. M. Veraart [Pays-Bas] | Lymphedema, cardiac septal defects, and characteristic facies: Possible new case of Irons–Bianchi syndrome |
| 007E46 (2005) |
Subash Babu ; V. Kumaraswami ; Thomas B. Nutman | Transcriptional Control of Impaired Th1 Responses in Patent Lymphatic Filariasis by T-Box Expressed in T Cells and Suppressor of Cytokine Signaling Genes |
| 008626 (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 |
| 008657 (2004) |
Naoyuki Miura [Japon] | [Multiple roles of forkhead genes in development and metabolism]. |
| 008707 (2004) |
Brett M. Hosking [Australie] ; S-C Mary Wang ; Meredith Downes ; Peter Koopman ; George E O. Muscat | The VCAM-1 gene that encodes the vascular cell adhesion molecule is a target of the Sry-related high mobility group box gene, Sox18. |
| 008829 (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. |
| 008865 (2004) |
Cathy Shea [États-Unis] ; David Hough ; Jianping Xiao ; George Tzertzinis ; Claude V. Maina | An rxr/usp homolog from the parasitic nematode, Dirofilaria immitis. |
| 008C75 (2004) |
Cagri Yildirim-Toruner [États-Unis] ; Kavitha Subramanian [États-Unis] ; Lamya El Manjra [États-Unis] ; Emily Chen [États-Unis] ; Stanley Goldstein ; Emilia Vitale [États-Unis, Italie] | A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema‐distichiasis syndrome associated with renal disease and diabetes mellitus |
| 008E38 (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. |
| 008E67 (2003) |
Michael S. Pepper [Suisse] | Literature watch. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome. |
| 008F12 (2003) |
David H. Gorski [États-Unis] ; Kenneth Walsh | Control of vascular cell differentiation by homeobox transcription factors. |
| 009136 (2003) |
Benjamin M. Kriederman ; 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 [Royaume-Uni] ; Brian P. Brooks [États-Unis] ; Thomas W. Glover | FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome |
| 009255 (2003) |
Alexandre Irrthum [États-Unis] ; Koenraad Devriendt [Belgique] ; David Chitayat [États-Unis] ; Gert Matthijs [Belgique] ; Conrad Glade [Pays-Bas] ; Peter M. Steijlen [Pays-Bas] ; Jean-Pierre Fryns [Belgique] ; Maurice A. M. Van Steensel [Pays-Bas] ; Miikka Vikkula [États-Unis] | Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia |
| 009277 (2003) |
Kara L. Levinson [États-Unis] ; Eleanor Feingold ; Robert E. Ferrell ; Thomas W. Clover ; Elias I. Traboulsi ; David N. Finegold | Age of onset in hereditary lymphedema |
| 009424 (2002) |
Marika J. Karkkainen [Finlande] ; Kari Alitalo [Finlande] | Lymphatic endothelial regulation, lymphoedema, and lymph node metastasis. |
| 009592 (2002) |
Robert E. Ferrell [États-Unis] | Research Perspectives in Inherited Lymphatic Disease |
| 009721 (2002) |
M. Bahuau [France] ; C. Houdayer ; M. Tredano ; V. Soupre [France] ; R. Couderc ; M-P Vazquez [France] | FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate |
| 009791 (2002) |
G. Brice [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; R. Bell [Royaume-Uni] ; J R O. Collin [Royaume-Uni] ; A H Child [Royaume-Uni] ; A F Brady [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; K G Burnand [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Peter Mortimer (dermatologue) [Royaume-Uni] ; V A Murday [Royaume-Uni] | Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24 |
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