Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Houssine Azeddoug"'
Autor:
Fatiha Salmi, Fatima Maachi, Amal Tazzite, Rachid Aboutaib, Jamal Fekkak, Houssine Azeddoug, Hassan Jouhadi
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0254101 (2021)
Prostate cancer is the most common male cancer in Morocco. Although sporadic forms account for a large proportion of patients, familial forms of prostate cancer are observed in 20% of cases and about 5% are due to hereditary transmission. Indeed, ger
Externí odkaz:
https://doaj.org/article/f267dd16896d42109772f469e8b5d099
Autor:
Sellama Nadifi, Asmâa Naim, Hassan Jouhadi, Abdellatif Benider, Houssine Azeddoug, Amal Tazzite
Publikováno v:
BMC Research Notes
Background BRCA1 and BRCA2 genes explain a large part of hereditary breast cancer. Several studies have shown that BRCA1 and BRCA2 tumors exhibit some specific morphological and immunohistochemical characteristics. The aim of our study is to compare
Autor:
Hanane Bellayou, Mohamed Abdou Rafai, Houssine Azeddoug, Ilham Slassi, Sellama Nadifi, Mehdi Karkouri, Khalil Hamzi
Publikováno v:
Journal of Biomedicine and Biotechnology
Journal of Biomedicine and Biotechnology, Vol 2009 (2009)
Journal of Biomedicine and Biotechnology, Vol 2009 (2009)
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive disorders caused by mutations of the DMD gene located at Xp21. In DMD patients, dystrophin is virtually absent; whereas BMD patients have 10% to 40% of the n
Publikováno v:
Hearing Research. 210:80-84
Deafness is a heterogeneous disorder showing different pattern of inheritance and involving a multitude of different genes. Mutations in the gene, GJB2 Gap junction type 1), encoding the gap junction protein connexin-26 on chromosome 13q11 may be res
Autor:
Sellama Nadifi, M. M. de Pancorbo, Maite Alvarez-Alvarez, Houssine Azeddoug, Faiza Chbel, C Martı́nez-Bouzas, M.-J. Rodriguez-Tojo
Publikováno v:
Russian Journal of Genetics. 39:1184-1190
Alu elements are the largest family of short tandem interspersed elements (SINEs) in human who have arisen to a copy number with an excess of 500 000 copies per haploid human genome and mobilize through an RNAse polymerase III derived transcript in a
Publikováno v:
European Journal of Plant Pathology. 108:155-162
The coat protein gene and part of the intergenic region of the RNA 3 of several isolates of Citrus variegation virus (CVV) producing either infectious variegation or crinkly leaf symptoms were amplified by RT-PCR, cloned and sequenced. Some isolates
Autor:
Abdelkarim Belkebir, Houssine Azeddoug
Publikováno v:
Microbiological research. 168(2)
Most of type II restriction endonucleases show an absolute requirement for divalent metal ions as cofactors for DNA cleavage. While Mg 2+ is the natural cofactor other metal ions can substitute it and mediate the catalysis, however Ca 2+ (alone) only
Autor:
Houssine Azeddoug, Abdelkarim Belkebir
Publikováno v:
ISRN Biochemistry
Requirement of divalent cations for DNA cleavage is a general feature of type II restriction enzymes with the exception of few members of this group. A new type II restriction endonuclease has been partially purified from Lactococcus lactis KLDS4. Th
Autor:
Hakima Yahia, Redouane Boulouiz, Adil Laouina, Faiza Chbel, Brahim El Houate, Houssine Azeddoug
Publikováno v:
Forensic science international. Genetics. 5(1)
Allele frequencies and population data for 17 Y-STR loci included in the AmpFlSTR ® Y-filer™ PCR amplification kit (Applied Biosystems, Foster City, USA), that permit the simultaneous amplification of all the markers included in the actually used
Autor:
M. Benomar, Anwar Benomar, Abdelilah Laraqui, Rachid Benzidia, Seddik Fellat, Abdenbi Bendris, Abdellatif Allami, Nizar El Kadiri, Houssine Azeddoug, N. Bennouar, Amal El Jaffali
Publikováno v:
Journal of Biomedicine and Biotechnology
Journal of Biomedicine and Biotechnology, Vol 2007 (2007)
Journal of Biomedicine and Biotechnology, Vol 2007 (2007)
Increased plasma total homocysteine (tHcy) levels have been shown to be a risk factor for coronary artery disease (CAD). The common methylenetetrahydrofolate reductase C677T (MTHFR C677T) polymorphism has been reported to be a strong predictor of mil