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Search references for FOXC2. Phrases containing FOXC2
See searches and references containing FOXC2!FOXC2
Protein-coding gene in the species Homo sapiens
Forkhead box protein C2 (FOXC2) also known as forkhead-related protein FKHL14 (FKHL14), transcription factor FKH-14, or mesenchyme fork head protein 1
FOXC2
Medical condition
Lymphedema–distichiasis syndrome is a medical condition associated with the FOXC2 gene. People with this hereditary condition have a double row of eyelashes
Lymphedema–distichiasis syndrome
Lymphedema–distichiasis_syndrome
Non-coding RNA in the species Homo sapiens
FOXC2 antisense RNA 1 is a protein that in humans is encoded by the FOXC2-AS1 gene. "Human PubMed Reference:". National Center for Biotechnology Information
FOXC2-AS1
Medical condition
STHAG3 3.3 FOXC1 Axenfeld syndrome 3 Iridogoniodysgenesis, dominant type FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior
Pitt–Hopkins_syndrome
Lymphedema commonly located in the legs
been linked to a mutations in the 'forkhead' family transcription factor (FOXC2) gene located on the long arm of chromosome 16 (16q24.3). About 2000 cases
Milroy's_disease
Protein-coding gene in the species Homo sapiens
regulation of embryonic and ocular development. FOXC1 and its close relative, FOXC2 are both critical components in the development of the heart and blood vessels
Forkhead_box_C1
Medical condition
been linked to a mutations in the ‘forkhead’ family transcription factor (FOXC2) gene located on the long arm of chromosome 16 (16q24.3). It is the most
Meige_disease
Medical condition in which superficial veins become large and twisted
Ed. Ng MY, Andrew T, Spector TD, Jeffery S (March 2005). "Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected
Varicose_veins
Human chromosome
member B FBRS: Probably fibrosin-1 long transcript protein FOXC2-AS1: encoding protein FOXC2 antisense RNA 1 GLG1: Golgi apparatus protein 1 HBAP1: Hemoglobin
Chromosome_16
Lymphatic-like vessel in the eye
lymphatic endothelium, including the expression of PROX1, VEGFR3, CCL21, FOXC2, but lacked the expression of LYVE1 and PDPN. It develops via a unique mechanism
Schlemm's_canal
Academic journal
Morikawa, M. Heglind, S. Enerback, T. Ezaki and J. Tamaoki 59 501-514 2017 Foxc2 influences alveolar epithelial cell differentiation during lung development
Development, Growth & Differentiation
Development,_Growth_&_Differentiation
Medical condition
STHAG3 3.3 FOXC1 Axenfeld syndrome 3 Iridogoniodysgenesis, dominant type FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior
Campomelic_dysplasia
Type of congenital heart defect
this gene have been associated with TOF, accounting for 2.4% of all cases. FOXC2 is another gene involved in embryonic development of the cardiac system
Tetralogy_of_Fallot
ENSG00000054598 Forkhead Known motif – High-throughput in vitro [244] WRWRTMAAYAW FOXC2 ENSG00000176692 Forkhead Known motif – High-throughput in vitro [245] WAHRTMAAYAWW
List of human transcription factors
List_of_human_transcription_factors
Protein family
promotes mTORC2-mediated phosphorylation of Akt1 to suppress expression of FoxC2 and stimulate adipocyte differentiation". Science Signaling. 6 (257): ra2
BSD_domain
Biological process in animal connective tissue
Twist, Goosecoid, TCF4 (also known as E2.2), homeobox protein SIX1 and FOXC2 (fork-head box protein C2) repress E-cadherin indirectly. SNAIL and ZEB
Epithelial–mesenchymal transition
Epithelial–mesenchymal_transition
Family of transcription factors involved in anatomical development
Hepatocyte nuclear factors.) FOXB1, FOXB2 FOXC1 (associated with glaucoma), FOXC2 (varicose veins) FOXD1, FOXD2, FOXD3 (vitiligo), FOXD4, FOXD4L1, FOXD4L3
FOX_proteins
Electric current produced in living cells
Kanady, J. D; Munger, S. J; Witte, M. H; Simon, A. M (2015). "Combining Foxc2 and Connexin37 deletions in mice leads to severe defects in lymphatic vascular
Developmental_bioelectricity
Protein-coding gene in the species Homo sapiens
characteristics. GSC, along with other transcription factors like Twist, FOXC2, and Snail, induce epithelial to mesenchymal transitions by regulating the
Homeobox_protein_goosecoid
Medical condition
STHAG3 3.3 FOXC1 Axenfeld syndrome 3 Iridogoniodysgenesis, dominant type FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior
Tricho-rhino-phalangeal syndrome Type 1
Tricho-rhino-phalangeal_syndrome_Type_1
arachnodactyly Fibulin-4 Fibulin-4 Cutis laxa Fibulin-5 Fibulin-5 Cutis laxa FOXC2 Lymphedema–distichiasis syndrome Meige lymphedema GALNT3 Familial tumoral
List of genes mutated in cutaneous conditions
List_of_genes_mutated_in_cutaneous_conditions
Medical condition
factor contributes to controlling the expression of two genes, PROX1 and FOXC2, which are required for the proper development of the lymphatic system,
GATA2_deficiency
Protein-coding gene in the species Homo sapiens
promotes mTORC2-mediated phosphorylation of Akt1 to suppress expression of FoxC2 and stimulate adipocyte differentiation". Science Signaling. 6 (257): ra2
SYAP1
Breast cancer subtype
pathways in BLBC leads to the expression of EMT-related transcription factors FOXC2, Twist, Slug, Snail, and LBX1, and then resulting in down-regulation of
Basal-like_carcinoma
necrotic and decays. Using a patented cocktail of plasmids (Etv2, Fli1, Foxc2, or EFF), these factors were delivered to the tissue above the surgery site
Tissue_nanotransfection
with renal disease and diabetes mellitus; 153400; FOXC2 Lymphedema–distichiasis syndrome; 153400; FOXC2 Lymphoma, non-Hodgkin; 605027; PRF1 Lymphoma, non-Hodgkin
List_of_OMIM_disorder_codes
Cancer cells with features of normal cells
Hartwell K, Richardson AL, Weinberg RA (June 2007). "Mesenchyme Forkhead 1 (FOXC2) plays a key role in metastasis and is associated with aggressive basal-like
Cancer_stem_cell
French-British biologist
Tsutomu; Relaix, Frédéric; Buckingham, Margaret E. (December 2009). "Pax3:Foxc2 Reciprocal Repression in the Somite Modulates Muscular versus Vascular Cell
Margaret_Buckingham
Q99853 5791 FOXB2 HGNC:23315; Q5VYV0 5792 FOXC1 HGNC:3800; Q12948 5793 FOXC2 HGNC:3801; Q99958 5794 FOXD1 HGNC:3802; Q16676 5795 FOXD2 HGNC:3803; O60548
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
FOXC2
FOXC2
FOXC2
FOXC2
Boy/Male
English
Meadow of the hares.. Surname.
Girl/Female
Muslim
Varnam
Girl/Female
Gujarati, Hawaiian, Hebrew, Hindu, Indian, Jain, Kannada, Malayalam, Marathi, Oriya, Punjabi, Sanskrit, Sikh, Tamil, Telugu, Zimbabwe
Kindness; Mercy; Pity
Surname or Lastname
English (Bristol)
English (Bristol) : variant spelling of Pullen.
Girl/Female
Arabic, Muslim
Angel; Diminutive of Malaka
Boy/Male
Norse
Fighter.
Boy/Male
Indian, Punjabi, Sikh
Virtues of Righteousness
Boy/Male
Australian, Chinese, Hebrew, Jewish
Original Name of the Father of the People; Father of Many; He who is High is Father; Father of a Multitude
Boy/Male
Indian
Praise of almighty Allah, Thanks to the graceful and merciful Allah
Boy/Male
Indian, Punjabi, Sikh
Perfect One; Satisfied
FOXC2
FOXC2
FOXC2
FOXC2
FOXC2