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biomedicina slovenica |
"CONNEXINS" : 13
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Pfarrer Christiane; Bridger Philip S.; Leiser Rudolf
Demonstration of connexins in cell cultures of bovine placenta
2007 ►
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Holzer Lukas A; Cör Andrej; Holzer Gerold
Expression of gap junction proteins connexins 26, 30, and 43 in Dupuytren's disease
2014 ►
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Galindo Ruth C; Ayllon Nieves; Strašek-Smrdel Katja; Avšič-Županc Tatjana
Gene expression profile suggests that pigs (Sus scrofa) are susceptible to Anaplasma phagocytophilum but control infection
2012 ►
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Fakin Ana; Zupan Andrej; Glavač Damjan; Hawlina M
Combination of retinitis pigmentosa and hearing loss caused by a novel mutation in PRPH2 and a known mutation in GJB2: importance for differential diagnosis of Usher syndrome
2012 ►
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Resnik Nataša; Veranič Peter
Cell junctions as membrane raft domains
2012 ►
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Battelino Saba; Rudolf Gorazd; Žargi Miha; Trebušak-Podkrajšek Katarina; Peterlin Borut
Connexin 26 (GJB2) and connexin 30 del(GJB6-D13S1830) mutations in Slovenians with prelingual non-syndromic deafness
2011 ►
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Rudolf Gorazd; Peterlin Borut
Genetska epidemiologija mutacij v genih GJB2 in GJB6 v populaciji prirojene senzorinevralne gluhosti v Sloveniji
2010 ►
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Zaputovic Sanja; Stanojevic Milan; Medica Igor; Peterlin Borut; Petrovic Oleg
Incidence of the 35delG/GJB2 mutation in low-risk newborns
2008 ►
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Battelino S; Žargi M; Repič-Lampret B
Gluhost in genetika - naše izkušnje s preiskavo gena GJB2 za koneksin 26
[Deafness and genetics - our experience with investigation of gene GJB2 for connexin 26]
2006 ►
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Medica Igor; Rudolf Gorazd; Prpić Igor; Stanojević Milan; Peterlin Borut
Incidence of the del35G/GJB2 mutation in Croatian newborns with hearing impairment
2005 ►
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Leonardis Lea; Zidar Janez; Peterlin Borut
Populacijska študija najpogostejših demielinizacijskih bolezni Charcot-Marie-Tooth v Sloveniji
[The most frequent types of demyelinative Charot-Marie-Tooth disease in Slovenia: a population-based study]
2003 ►
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Hatsell SJ; Kelsell DP
The diffuse palmoplantar keratodermas
2000 ►
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Leonardis L; Zidar J; Popović M; Timmerman V; Loefgren A; van Broeckhoven C; Butinar D
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family
2000 ►
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