Andrej Nikosjkov

Publikationer
Populärvetenskap och samverkan

Artiklar

Article: MOLECULES. 2022;27(7):2350

Non-Peptide Opioids Differ in Effects on Mu-Opioid (MOP) and Serotonin 1A (5-HT_1A) Receptors Heterodimerization and Cellular Effectors (Ca²⁺, ERK 1/2 and p38) Activation

Radoi V; Jakobsson G; Palada V; Nikosjkov A; Druid H; Terenius L; Kosek E; Vukojevic V
Article: NATURE GENETICS. 2019;51(12):1723-1731

WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating

Scholz BA; Sumida N; de Lima CDM; Chachoua I; Martino M; Tzelepis I; Nikoshkov A; Zhao H; Mehmood R; Sifakis EG; Bhartiya D; Gondor A; Ohlsson R
Article: INTERNATIONAL JOURNAL OF ONCOLOGY. 2015;46(1):107-112

Expression pattern of the PRDX25 RAB1A, RAB1B, RAB5A and RAB25 genes in normal and cancer cervical tissues

Nikoshkov A; Broliden K; Attarha S; Sviatoha V; Hellstrom A-C; Mints M; Andersson S
Article: PLOS ONE. 2012;7(5):e37429

Automated solid-phase subcloning based on beads brought into proximity by magnetic force.

Hudson EP; Nikoshkov A; Uhlen M; Rockberg J
Article: DIABETES-METABOLISM RESEARCH AND REVIEWS. 2011;27(5):470-479

Stability of mitochondrial DNA against reactive oxygen species (ROS) generated in diabetes

Savu O; Sunkari VG; Botusan IR; Gruenler J; Nikoshkov A; Catrina S-B
Article: ELECTROMAGNETIC BIOLOGY AND MEDICINE. 2011;30(2):80-85

Effects of a low-intensity electromagnetic field on fibroblast migration and proliferation

Sunkari VG; Aranovitch B; Portwood N; Nikoshkov A
Article: EPIGENETICS. 2011;6(4):405-409

Epigenetic DNA methylation in the promoters of the Igf1 receptor and insulin receptor genes in db/db mice

Nikoshkov A; Sunkari V; Savu O; Forsberg E; Catrina S-B; Brismar K
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2008;105(2):786-791

Opioid neuropeptide genotypes in relation to heroin abuse: Dopamine tone contributes to reversed mesolimbic proenkephalin expression

Nikoshkov A; Drakenberg K; Wang X; Horvath MC; Keller E; Hurd YL
Article: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 2006;351(2):383-386

p53 splice variants generated by atypical mRNA processing confer complexity of p53 transcripts in the human brain.

Nikoshkov A; Hurd YL
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2006;103(20):7883-7888

μ opioid receptor A118G polymorphism in association with striatal opioid neuropeptide gene expression in heroin abusers

Drakenberg K; Nikoshkov A; Horvath MC; Fagergren P; Gharibyan A; Saarelainen K; Rahman S; Nylander I; Bakalkin G; Rajs J; Keller E; Hurd YL
Article: FASEB JOURNAL. 2005;19(9):1543-1545

Prodynorphin transcripts and proteins differentially expressed and regulated in the adult human brain

Nikoshkov A; Hurd YL; Yakovleva T; Bazov I; Marinova Z; Cebers G; Pasikova N; Gharibyan A; Terenius L; Bakalkin G
Article: CLINICAL AND EXPERIMENTAL IMMUNOLOGY. 2003;107(2):341-346

21-hydroxylase autoantibodies in adult patients with endocrine autoimmune diseases are highly specific for Addison's disease. Belgian Diabetes Registry.

Falorni A; Laureti S; Nikoshkov A; Picchio ML; Hallengren B; Vandewalle CL; Gorus FK; Tortoioli C; Luthman H; Brunetti P; Santeusanio F
Article: CLINICAL ENDOCRINOLOGY. 2001;54(6):827-834

A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility

Giwercman YL; Nikoshkov Å; Byström B; Pousette A; Arver S; Wedell A
Article: HUMAN MOLECULAR GENETICS. 2000;9(14):2149-2158

Insulin-degrading enzyme identified as a candidate diabetes susceptibility gene in GK rats

Fakhrai-Rad H; Nikoshkov A; Kamel A; Fernström M; Zierath JR; Norgren S; Luthman H; Galli J
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2000;66(2):453-460

A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-q26.

Ciccarese M; Pacifico A; Tonolo G; Pintus P; Nikoshkov A; Zuliani G; Fellin R; Luthman H; Maioli M
Article: HORMONE RESEARCH IN PAEDIATRICS. 2000;53(2):83-88

Response to treatment in patients with partial androgen insensitivity due to mutations in the DNA-binding domain of the androgen receptor

Giwercman YL; Nikoshkov A; Lindsten K; Byström B; Pousette Å; Knudtzon J; Alm J; Wedell A
Article: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 1999;257(2):384-390

Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21)

Lajic S; Nikoshkov A; Holst M; Wedell A
Article: JOURNAL OF IMMUNOLOGY. 1999;162(4):2422-2426

A conformation-dependent epitope in Addison's disease and other endocrinological autoimmune diseases maps to a carboxyl-terminal functional domain of human steroid 21-hydroxylase

Nikoshkov A; Falorni A; Lajic S; Laureti S; Wedell A; Lernmark Å; Luthman H
Article: HUMAN GENETICS. 1998;103(4):529-531

Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome

Giwercman YL; Nikoshkov A; Lindsten K; Bystrom B; Pousette A; Chibalin AV; Arvidsson S; Tiulpakov A; Semitcheva TV; Peterkova V; Hagenfeldt K; Ritzen EM; Wedell A
Article: GENOMICS. 1998;49(3):401-410

Structure and transcription regulation of the human insulin-like growth factor binding protein 4 gene (IGFBP4)

Zazzi H; Nikoshkov A; Hall K; Luthman H
Article: JOURNAL OF BIOLOGICAL CHEMISTRY. 1998;273(11):6163-6165

Naturally occurring mutants of human steroid 21-hydroxylase (P450c21) pinpoint residues important for enzyme activity and stability

Nikoshkov A; Lajic S; Vlamis-Gardikas A; Tranebjaerg L; Holst M; Wedell A; Luthman H
Article: HUMAN GENETICS. 1997;99(6):704-709

A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction

Lajic S; Levo A; Nikoshkov A; Lundberg Y; Partanen J; Wedell A
Article: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 1997;82(1):194-199

Synergistic effect of partially inactivating mutations in steroid 21-hydroxylase deficiency

Nikoshkov A; Lajic S; Holst M; Wedell A; Luthman H
Article: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 1995;80(9):2752-2755

HIGH DIAGNOSTIC-ACCURACY FOR IDIOPATHIC ADDISONS-DISEASE WITH A SENSITIVE RADIOBINDING ASSAY FOR AUTOANTIBODIES AGAINST RECOMBINANT HUMAN 21-HYDROXYLASE

FALORNI A; NIKOSHKOV A; LAURETI S; GRENBACK E; HULTING AL; CASUCCI G; SANTEUSANIO F; BRUNETTI P; LUTHMAN H; LERNMARK A
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Corrigendum: NATURE GENETICS. 2020;52(11):1265

WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating (vol 51, pg 1723, 2019)

Scholz BA; Sumida N; de Lima CDM; Chachoua I; Martino M; Tzelepis I; Nikoshkov A; Zhao H; Mehmood R; Sifakis EG; Bhartiya D; Gondor A; Ohlsson R

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