A. Errami

发表

Discovery of high-grade REE-Nb-Fe mineralization associated with calciocarbonatite in south Morocco

U. Schwarz-Schampera, M. Sitnikova, M. Bau, 2020 .

Brca2 (XRCC11) Deficiency Results in Radioresistant DNA Synthesis and a Higher Frequency of Spontaneous Deletions

R. Kanaar, P. V. van Buul, J. Essers, 2002, Molecular and Cellular Biology.

Evidence for genetic heterogeneity in D‐2‐hydroxyglutaric aciduria

B. Maranda, J. Abdenur, S. Korman, 2010, Human mutation.

A new X-ray sensitive CHO cell mutant of ionizing radiation group 7,XR-C2, that is defective in DSB repair but has only a mild defect in V(D)J recombination.

D. Gell, A. Friedl, P. Lohman, 2000, Mutation research.

First evidence for Cambrian rift-related magmatism in the West African Craton margin: The Derraman Peralkaline Felsic Complex

A. Michard, F. Bea, P. Montero, 2016 .

MLPA diagnostics of complex microbial communities: relative quantification of bacterial species in oral biofilms.

W. Crielaard, R. V. van Spanning, J. T. ten Cate, 2008, Journal of microbiological methods.

Contrasting SHRIMP U–Pb zircon ages of two carbonatite complexes from the peri-cratonic terranes of the Reguibat Shield: Implications for the lateral extension of the West African Craton

A. Cambeses, F. Bea, P. Montero, 2016 .

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2

Hans Joenje, Bing Xia, Weidong Wang, 2007, Nature Genetics.

Epigenetic events of disease progression in head and neck squamous cell carcinoma.

J. Schouten, M. Benninger, A. Nygren, 2006, Archives of otolaryngology--head & neck surgery.

Petrogenesis of Derraman Peralkaline granite (Oulad Dlim Massif, West African Craton Margin, Morocco): New constraints from zircon Hf and O isotopic compositions

F. González-Lodeiro, A. Cambeses, F. Bea, 2018, Comptes Rendus Geoscience.

Detailed analysis of 22q11.2 with a high density MLPA probe set

T. Shaikh, J. Biegel, J. Vorstman, 2008, Human mutation.

Genetic subtyping of Fanconi anemia by comprehensive mutation screening

G. Pals, N. Ameziane, H. Joenje, 2008, Human mutation.

MS-MLPA: an attractive alternative laboratory assay for robust, reliable, and semiquantitative detection of MGMT promoter hypermethylation in gliomas

P. Wesseling, J. Jeuken, A. Sijben, 2007, Laboratory Investigation.

Screening for large mutations of the NF2 gene

M. Tatagiba, L. Kluwe, V. Mautner, 2005, Genes, chromosomes & cancer.

Ku86 defines the genetic defect and restores X-ray resistance and V(D)J recombination to complementation group 5 hamster cell mutants

G. Chu, E. Hendrickson, M. Zdzienicka, 1996, Molecular and cellular biology.

Methylation-Specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences

J. Schouten, Q. Waisfisz, N. Ameziane, 2005, Nucleic acids research.

Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA)

V. Mcconnell, A. Donaldson, T. Lourenço, 2013, BMC Medical Genetics.

Screening of congenital heart disease patients using multiplex ligation‐dependent probe amplification: Early diagnosis of syndromic patients

T. Werge, J. Schouten, N. Tommerup, 2012, American journal of medical genetics. Part A.

Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancer.

Philippe Thuillier, Abdellatif Errami, J. Cain, 2006, Cancer research.

Hypermethylation of the FANCC and FANCL Promoter Regions in Sporadic Acute Leukaemia

Q. Waisfisz, D. Reinhardt, C. Zwaan, 2008, Cellular oncology : the official journal of the International Society for Cellular Oncology.

A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy

T. Obata, H. Osaka, K. Kurosawa, 2010, Journal of Inherited Metabolic Disease.

Identification of genomic deletions of the APC gene in familial adenomatous polyposis by two independent quantitative techniques.

H. Grönberg, G. Kanter-Smoler, E. Holmberg, 2004, Genetic testing.

XR-C1, a new CHO cell mutant which is defective in DNA-PKcs, is impaired in both V(D)J coding and signal joint formation

Stephen P. Jackson, Mitsuo Oshimura, Paul H. M. Lohman, 1998, Nucleic Acids Res..

Concurrent methylation of promoters from tumor associated genes predicts outcome in acute myeloid leukemia

Quinten Waisfisz, Johannes Berkhof, Abdellatif Errami, 2008, Leukemia & lymphoma.

Discovery of antiskarn-hosted strategic metal mineralization in the Upper Cretaceous Twihinate carbonatite intrusion (West African Craton Margin, Moroccan Sahara)

M. Jébrak, G. Levresse, F. Bigot, 2022, Ore Geology Reviews.

A single amino acid substitution in DNA-PKcs explains the novel phenotype of the CHO mutant, XR-C2.

M. Zdzienicka, W. Wang, K. Meek, 2002, Nucleic Acids Research.

Molecular and biochemical characterization of new X-ray-sensitive hamster cell mutants defective in Ku80.

B. Morolli, P. Lohman, A. Errami, 1998, Nucleic acids research.

Lack of large genomic deletions in BRIP1, PALB2, and FANCD2 genes in BRCA1/2 negative familial breast cancer

Q. Waisfisz, H. Meijers-Heijboer, M. Adank, 2009, Breast Cancer Research and Treatment.

An overview of L‐2‐hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype–phenotype study

D. Zafeiriou, J. Celli, J. D. den Dunnen, 2010, Human mutation.

Sequential gene promoter methylation during HPV-induced cervical carcinogenesis

J. Schouten, C. Meijer, P. Snijders, 2007, British Journal of Cancer.

Clinical and histomolecular endometrial tumor characterization of patients at-risk for Lynch syndrome in South of Brazil

J. Prolla, H. Bock, M. Saraiva-Pereira, 2010, Familial Cancer.