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Literature citations Results

Citation
Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy.

Nemethova M., Radvanszky J., Kadasi L., Ascher D.B., Pires D.E., Blundell T.L., Porfirio B., Mannoni A., Santucci A., Milucci L. et al.

Eur. J. Hum. Genet. 24:66-72(2016) · Mapped (3)

Transient localization of the Arp2/3 complex initiates neuronal dendrite branching in vivo.

Sturner T., Tatarnikova A., Mueller J., Schaffran B., Cuntz H., Zhang Y., Nemethova M., Bogdan S., Small V., Tavosanis G.

Development 146:0-0(2019) · Mapped (12)

Thirty-nine novel neurofibromatosis 1 (NF1) gene mutations identified in Slovak patients.

Nemethova M., Bolcekova A., Ilencikova D., Durovcikova D., Hlinkova K., Hlavata A., Kovacs L., Kadasi L., Zatkova A.

Ann. Hum. Genet. 77:364-379(2013) · UniProtKB (1) · Mapped (11)

PCR cloning and sequencing of the coding portion of the thioredoxin-encoding gene from Streptomyces aureofaciens BMK.

Labudova O., Nemethova M., Turna J., Kollarova M.

Gene 138:263-264(1994) · UniProtKB (1)

Nine-amino-acid transactivation domain: establishment and prediction utilities.

Piskacek S., Gregor M., Nemethova M., Grabner M., Kovarik P., Piskacek M.

Genomics 89:756-768(2007) · UniProtKB (19)

Mutation screening of the HGD gene identifies a novel alkaptonuria mutation with significant founder effect and high prevalence.

Sakthivel S., Zatkova A., Nemethova M., Surovy M., Kadasi L., Saravanan M.P.

Ann. Hum. Genet. 78:155-164(2014) · Mapped (3)

MTSS1 is a metastasis driver in a subset of human melanomas.

Mertz K.D., Pathria G., Wagner C., Saarikangas J., Sboner A., Romanov J., Gschaider M., Lenz F., Neumann F., Schreiner W. et al.

Nat Commun 5:3465-3465(2014) · Mapped (7)

Inhibitory signalling to the Arp2/3 complex steers cell migration.

Dang I., Gorelik R., Sousa-Blin C., Derivery E., Guerin C., Linkner J., Nemethova M., Dumortier J.G., Giger F.A., Chipysheva T.A. et al.

Nature 503:281-284(2013) · UniProtKB (4) · Mapped (1)

Identification of 11 novel homogentisate 1,2 dioxygenase variants in alkaptonuria patients and establishment of a novel LOVD-based HGD mutation database.

Zatkova A., Sedlackova T., Radvansky J., Polakova H., Nemethova M., Aquaron R., Dursun I., Usher J.L., Kadasi L.

JIMD Rep. 4:55-65(2012) · UniProtKB (1)

Cofilin cooperates with fascin to disassemble filopodial actin filaments.

Breitsprecher D., Koestler S.A., Chizhov I., Nemethova M., Mueller J., Goode B.L., Small J.V., Rottner K., Faix J.

J. Cell. Sci. 124:3305-3318(2011) · Mapped (3)

Clustering of mutations in the 5' tertile of the NF1 gene in Slovakia patients with optic pathway glioma.

Bolcekova A., Nemethova M., Zatkova A., Hlinkova K., Pozgayova S., Hlavata A., Kadasi L., Durovcikova D., Gerinec A., Husakova K. et al.

Neoplasma 60:655-665(2013) · Mapped (12)

Brain-derived neurotrophic factor blood levels in two models of transient brain ischemia in rats.

Gottlieb M., Bonova P., Danielisova V., Nemethova M., Burda J., Cizkova D.

Gen. Physiol. Biophys. 32:139-142(2013) · Mapped (7)

Activities of endogenous antioxidant enzymes in the cerebrospinal fluid and the hippocampus after transient forebrain ischemia in rat.

Danielisova V., Gottlieb M., Nemethova M., Burda J.

J. Neurol. Sci. 253:61-65(2007) · Mapped (1)

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