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Profil bibliographique

P. Coullin

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

25Publications signalées
765Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Chromosomal and Genetic VariationsGlycosylation and Glycoproteins ResearchGestational Trophoblastic Disease StudiesPrenatal Screening and DiagnosticsGenomic variations and chromosomal abnormalities

Les publications récentes

Accès ouvert 2012 article OpenAlex

Les môles hydatiformes partielles au Maroc : étude épidémiologique et clinique

Houssine Boufettal, P. Coullin, S. Mahdaoui, Mohammed Noun et autres

This retrospective study reviewed cases of partial hydatidiform mole (PHM) diagnosed at the University Hospital in Casablanca from 2000 to 2010 in order to examine the epidemiological, clinical, therapeutic and progressive pathological factors associated with PHM. All PHM cases confirmed clinically and …

Maroc, fr (code pays fourni par la source)

6 citations Eastern Mediterranean Health Journal
2010 article OpenAlex

The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta

M. Noguer-Dance, Sayeda N Abu-Amero, Mohamed Al-Khtib, Antoine Lefevre et autres

Imprinted genes play crucial roles in mammalian development and disruption of their expression is associated with many human disorders including tumourigenesis; yet, the actual number of imprinted genes in the human genome remains a matter of debate. Here, we report on the …

fr (code pays fourni par la source)

335 citations Human Molecular Genetics
Accès ouvert 2009 article OpenAlex

NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation

C. Deveault, J. H. Qian, Wafaa Chebaro, Qiang Ao et autres

Human Molecular Genetics 2009 18(5): 888–897; doi:10.1093/hmg/ddn418 The authors would like to apologise for he following errors in the above article: The correct affiliation for Amira Mehio is Department of Pathology, McGill University Health Center, Montreal H3G 1A4, Canada In Table 1 …

33 citations Human Molecular Genetics
2008 article OpenAlex

Swine centromeric DNA repeats revealed by primed in situ (PRINS) labeling

Claire Rogel-Gaillard, H�l�ne Hayes, P. Coullin, P. Chardon et autres

In swine, distinct centromeric satellite DNA families have been described that correspond to either all the metacentric chromosomes except the Y (Mc1) or all the acrocentric chromosomes (Ac2). Using primed in situ (PRINS) labeling, we show here that primers derived from various …

Maroc, fr (code pays fourni par la source)

20 citations Cytogenetics and Cell Genetics
2006 article OpenAlex

High promoter hypermethylation frequency of p14/ARF in supratentorial PNET but not in medulloblastoma

M M Inda, J Muñoz, P. Coullin, Didier Fauvet et autres

AIMS: Medulloblastoma (MB) is the most common primitive neuroectodermal tumour (PNET) of the central nervous system. Although supratentorial PNET (sPNET) and MB are histologically similar, their clinical behaviour differs, sPNET being more aggressive than MB. The aim of this study was to …

fr, es (code pays fourni par la source)

28 citations Histopathology
Accès ouvert 2003 article OpenAlex

Cytogenetics, conserved synteny and evolution of chicken fucosyltransferase genes compared to human

P. Coullin, Richard P. M. A. Crooijmans, Valérie Fillon, Rosella Mollicone et autres

Fucosyltransferases appeared early in evolution, since they are present from bacteria to primates and the genes are well conserved. The aim of this work was to study these genes in the bird group, which is particularly attractive for the comprehension of the …

fr, nl (code pays fourni par la source)

6 citations Cytogenetic and Genome Research

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