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Identification of the novel mutation m.5658T>C in the mitochondrial tRNA(Asn) gene in a patient with myopathy, bilateral ptosis and ophthalmoparesis.Darunavir and ritonavir total and unbound plasmatic concentrations in HIV-HCV-coinfected patients with hepatic cirrhosis compared to those in HIV-monoinfected patientsLimb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene.Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndrome.Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy.Identification of androgen-regulated genes in mouse kidney by representational difference analysis and random arbitrarily primed polymerase chain reactionSex steroid regulation and identification of different transcription units of the SA gene in mouse kidney
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Q34572607-D10D558B-3D91-4D4F-8D58-1D9CFE049BFFQ36158135-BD6CFAB1-DC17-48E2-B435-A1129E7B10A6Q36789599-C25D08A3-14CD-4876-8C68-13BF75EE4C6EQ39080558-6392360C-22C7-4EAF-B183-563C0BF1984EQ55059717-14730B9D-BEF6-49BE-AFBA-C4E100B194D7Q74117421-03BD7012-453C-481B-94BB-E63779742C0EQ80961255-0091382B-3042-452C-BDFA-F5F143401621
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description
researcher
@en
wetenschapper
@nl
name
Maria Jesus Melià
@en
Melià MJ
@nl
type
label
Maria Jesus Melià
@en
Melià MJ
@nl
altLabel
Melià MJ
@en
prefLabel
Maria Jesus Melià
@en
Melià MJ
@nl
P106
P31
P496
0000-0002-6497-7289