Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
Probing the role of loop 2 in Ras function with unnatural amino acids.
|
8234268 |
1993 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
Effector domain mutations dissociate p21ras effector function and GTPase-activating protein interaction.
|
8246952 |
1993 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.
|
16474404 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.
|
16474404 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.
|
16474404 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.
|
16474404 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
Germline KRAS mutations cause Noonan syndrome.
|
16474405 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Germline KRAS mutations cause Noonan syndrome.
|
16474405 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype.
|
16773572 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GermlineCausalMutation
|
disease |
ORPHANET |
The cardiofaciocutaneous syndrome.
|
16825433 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We and others recently discovered novel germline KRAS mutations in individuals diagnosed with Noonan or cardio-facio-cutanous (CFC) syndrome, two clinically overlapping disorders characterized by short stature, distinct facial anomalies, heart defects, and other developmental abnormalities.
|
16921267 |
2006 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
We further defined the phenotypic spectrum associated with KRAS missense mutations and provided the first evidence of clinical differences in patients with KRAS mutations compared with Noonan syndrome affected individuals with heterozygous PTPN11 mutations and CFC patients carrying a BRAF, MEK1 or MEK1 alteration, respectively.
|
17056636 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
We further defined the phenotypic spectrum associated with KRAS missense mutations and provided the first evidence of clinical differences in patients with KRAS mutations compared with Noonan syndrome affected individuals with heterozygous PTPN11 mutations and CFC patients carrying a BRAF, MEK1 or MEK1 alteration, respectively.
|
17056636 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Germline mutations in KRAS have recently been identified in a small number of patients with Noonan syndrome and CFC.
|
17056636 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
Biomarker
|
disease |
CLINGEN |
We further defined the phenotypic spectrum associated with KRAS missense mutations and provided the first evidence of clinical differences in patients with KRAS mutations compared with Noonan syndrome affected individuals with heterozygous PTPN11 mutations and CFC patients carrying a BRAF, MEK1 or MEK1 alteration, respectively.
|
17056636 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We and others have recently discovered germline mutations in the KRAS gene in individuals diagnosed with Noonan and cardio-facio-cutaneous (CFC) syndrome, two clinically overlapping disorders characterized by short stature, distinct facial anomalies, heart defects, and other abnormalities.
|
17211612 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We have observed unusual transverse distal phalangeal creases in two patients, one with Costello syndrome (G12S mutation in the HRAS gene) and one with cardio-facio-cutaneous (CFC) syndrome or possibly Noonan syndrome (Q22E mutation in the KRAS gene).
|
17324647 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
In total, 35 of 56 (62.5%) patients with CFC syndrome had mutations (3 in KRAS, 24 in BRAF, and 8 in MAP2K1/2).
|
17366577 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Congenital ulcerating hemangioma in a baby with KRAS mutation and cardio-facio-cutaneous syndrome.
|
17551339 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
Biomarker
|
disease |
CLINGEN |
De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features.
|
17601930 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
Biomarker
|
disease |
CTD_human |
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.
|
17703371 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome.
|
17704260 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
Biomarker
|
disease |
CLINGEN |
Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome.
|
17704260 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We performed detailed biochemical and functional studies of three mutant K-Ras proteins (P34R, D153V, and F156L) found in individuals with Noonan syndrome and cardiofaciocutaneous syndrome.
|
17875937 |
2007 |
Cardio-facio-cutaneous syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Biochemical and functional characterization of germ line KRAS mutations.
|
17875937 |
2007 |