Results for allele translation from English to Maltese

allele
allel

patients with ugt1a1 allele
pazjenti bl-allel ugt1a1

this cyp2a6*4 allele is uncommon in the caucasian population.
dan l-allel ta' cyp2a6*4 mhux komuni fil-popolazzjoni kawkasi.

hla-a*3101 allele- european descent and japanese populations
allele hla-a*3101- popolazzjonijiet ta’ oriġini ewropea u Ġappuniża

female ovine animals carrying at least one arr allele and no vrq allele.
annimali ovini nisa li jġorru mill-inqas allel arr wieħed u ebda allel vrq.

the presence of hla-b*1502 allele in other ethnicities is negligible.
il-preżenza ta’ allel ta’ hla-b*1502 f’etniċitajiet oħrajn hija negliġibbli.

carriers of the slco1b1 gene c.521t>c allele have lower oatp1b1 activity.
trasportaturi tal-ġene slco1b1 c.521t>c allele għandhom attività oatp1b1 iktar baxxa.

the frequency of the hla-a*3101 allele varies widely between ethnic populations.
il-frekwenza tal-allele hla-a*3101 tvarja ħafna bejn popolazzjonijiet etniċi.

abacavir should not be used in patients known to carry the hla-b*5701 allele.
abacavir ma għandux jintuża f’pazjenti li huma magħrufa li għandhom l-allel hla- b*5701.

the bmx thxid braf assay is an allele-specific pcr performed on dna extracted from ffpe tumour tissue.
l-analiżi ta’ braf thxid bmx hija pcr speċifika għall-allele mwettqa fuq dna estratt minn tessut tat-tumur ffpe.

however, some patients with a suspected abc hypersensitivity reaction may not have the hla-b*5701 allele.
madankollu, xi pazjenti b’reazzjoni ta’ sensittività eċċessiva ta’ abc suspettata jista’ jkun li ma jkollhomx l-allele hla-b*5701.

svr rates were comparable regardless of age, race, gender, il28b allele status, or baseline hcv rna level.
ir-rati ta’ svr kienu komparabbli irrispettivament mill- età, ir-razza, is-sess, l-istatus allele il28b, jew il-livell hcv rna fil-linja bażi.

svr rates were comparable regardless of hiv regimen, age, race, gender, il28b allele status, or baseline hcv rna level.
ir-rati ta’ svr kienu komparabbli irrispettivament mill-kors tal-hiv, l-età, ir-razza, is-sess, l-istatus allele il28b, jew il-livell ta’ hcv rna fil-linja bażi.

individuals who are 7/7 homozygous for the ugt1a1*28 allele are at increased risk for neutropenia from non-liposomal irinotecan.
l-individwi li huma 7/7 omożigoti għall-allel ugt1a1*28 huma f’riskju akbar għal newtropenija minn irinotecan mhux lipożomali.

hla-a*3101 allele has a prevalence of 2 to 5% in european populations and about 10% in japanese population.
l-allele hla-a*3101 għandu prevalenza ta’ 2 sa 5% fil-popolazzjonijiet ewropej u madwar 10% fil-popolazzjoni Ġappuniża.

in a small number of patients without a functional cyp2c19 allele, significantly increased voriconazole exposures are expected (see section 4.5).
f’għadd żgħir ta’ pazjenti mingħajr allele cyp2c19 funzjonali, hu mistenni li jkun hemm żieda sinifikattiva fl-esponimenti għal voriconazole (ara sezzjoni 4.5).

study 6 evaluated 69 patients who were 6 years of age or older; 53 (76.8%) of patients had the f508del mutation in the second allele.
studju 6 evalwa 69 pazjent li kellhom 6 snin jew aktar; 53 (76.8%) tal-pazjenti kellhom il-mutazzjoni f508del fit-tieni allele.

other alleles associated with absent or reduced metabolism are less frequent and include cyp2c19*4, *5,
alleli oħra assoċjati ma' metaboliżmu assenti jew imnaqqas huma anqas frekwenti u jinkludu cyp2c19*4,