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searching for FGF3 10 found (19 total)

alternate case: fGF3

Michel aplasia (621 words) [view diff] exact match in snippet view article find links to article

(labyrinthine aplasia, microtia and microdontia), which is caused by mutation FGF3 gene on chromosome 11q13 which encodes fibroblast growth factor 3. Mode of

Cortactin (2,576 words) [view diff] exact match in snippet view article find links to article

and squamous cell carcinomas encompasses three CpG islands telomeric of FGF3, including the expressed gene EMS1". Genes Chromosomes Cancer. 6 (4): 222–31

Otic vesicle (814 words) [view diff] case mismatch in snippet view article find links to article

FGF and BMP signals help control patterning in the early otic vesicle. Fgf3 and Fgf10 are suggested to play a role in otic induction in mice, as were

Odontoma dysphagia syndrome (196 words) [view diff] exact match in snippet view article find links to article

years: odontoma-dysphagia syndrome is most likely caused by a microduplication of chromosome 11q13.3, including the FGF3 and FGF4 genes. Clin Oral Investig

Rhodesian Ridgeback (3,250 words) [view diff] exact match in snippet view article find links to article

Lindblad-Toh, K; Andersson, L; Andersson, G (November 2007). "Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus

Retinal ganglion cell (3,522 words) [view diff] exact match in snippet view article find links to article

process depends on a host of factors, ranging from signaling factors like FGF3 and FGF8 to proper inhibition of the Notch signaling pathway. Most importantly

Paracrine signaling (4,940 words) [view diff] case mismatch in snippet view article find links to article

FGFR Knockout Gene Survival Phenotype Fgf1 Viable Unclear Fgf3 Viable Inner ear, skeletal (tail) differentiation Fgf4 Lethal Inner cell mass proliferation

FADD (4,191 words) [view diff] exact match in snippet view article find links to article

syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma". Human Molecular

Dog coat genetics (9,474 words) [view diff] exact match in snippet view article find links to article

surrounding coat. The ridge is caused by a duplication of several genes (FGF3, FGF4, FGF 19, ORAOV1 and sometimes SNP), and ridge is dominant to non-ridged

Human betaretrovirus (3,388 words) [view diff] exact match in snippet view article find links to article

established for HBRV. The over-expression in human MCF7 cells of both WNT1 and FGF3 genes, main integration sites (INT) of MMTV in mouse, induces the synthesis