P. de Mazancourt

发表

Allele-Specific Amplification for the Diagnosis of Autosomal Recessive Spinal Muscular Atrophy

L. Viollet, Claire Ravard-Goulvestre, C. Boucly, 1999, Clinical chemistry and laboratory medicine.

A splicing donor site point mutation in intron 6 of the plasmin inhibitor (α2 antiplasmin) gene with heterozygous deficiency and a bleeding tendency

P. de Mazancourt, M. Dechavanne, M. Hanss, 2003, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

An integrated sample-in-answer-out microfluidic chip for rapid human identification by STR analysis.

James P Landers, Luc Chassagne, Anchi Tsuei, 2014, Lab on a chip.

Identification and localization of G protein subunits in human spermatozoa.

P. de Mazancourt, L. Weinstein, J. Hall, 1999, Molecular human reproduction.

Identification and localization of netrin-4 and neogenin in human first trimester and term placenta.

P. de Mazancourt, P. Rozenberg, M. Dakouane-Giudicelli, 2012, Placenta.

Discrepancies between forensic identification kits explained by a laser power supply shutdown.

P. de Mazancourt, Sylvaine Siméon, Catherine Puech, 2006, Forensic science international.

False homozygosities at various loci revealed by discrepancies between commercial kits: implications for genetic databases.

P. de Mazancourt, Magali Delamoye, C. Duverneuil, 2004, Forensic science international.

Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria

P. de Mazancourt, T. Mirault, A. Fischer, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

Thrombin generation in patients with factor XI deficiency and clinical bleeding risk

P. de Mazancourt, C. Négrier, Y. Dargaud, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

Genetic Polymorphisms Influence the Ovarian Response to rFSH Stimulation in Patients Undergoing In Vitro Fertilization Programs with ICSI

P. de Mazancourt, M. Benahmed, F. Vialard, 2012, PloS one.

[A case of dysfibrinogenemia without hemorrhagic diathesis or thromboembolism linked to a new mutation p.H103N in fibrinogen γ chain].

P. de Mazancourt, T. Lecompte, M. Hanss, 2013, Annales de biologie clinique.

Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes

P. de Mazancourt, M. Samama, H. Erdem, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Polymorphisms of human placental alkaline phosphatase are associated with in vitro fertilization success and recurrent pregnancy loss.

J. Gris, P. de Mazancourt, P. Laissue, 2014, The American journal of pathology.

Characterization of a severe hypofibrinogenemia induced by alteplase in two patients thrombolysed for stroke.

N. Nighoghossian, P. de Mazancourt, L. Derex, 2013, Thrombosis research.

Adiponectin and reproduction.

P. de Mazancourt, M. Dieudonné, E. Dos Santos, 2012, Vitamins and hormones.

cAMP-positive regulation of angiotensinogen gene expression and protein secretion in rat adipose tissue.

P. de Mazancourt, M. Dieudonné, Y. Giudicelli, 2004, American journal of physiology. Endocrinology and metabolism.

Androgen regulation and site specificity of angiotensinogen gene expression and secretion in rat adipocytes.

P. de Mazancourt, Y. Giudicelli, V. Serazin-Leroy, 2000, American journal of physiology. Endocrinology and metabolism.

Effects of adiponectin on human trophoblast invasion.

P. de Mazancourt, M. Dieudonné, E. Dos Santos, 2010, The Journal of endocrinology.

Differences in type II, IV, V and VI adenylyl cyclase isoform expression between rat preadipocytes and adipocytes.

P. de Mazancourt, Y. Giudicelli, V. Serazin-Leroy, 2001, Biochimica et biophysica acta.

Mutant α-Subunit of the G Protein G12 Activates Proliferation and Inhibits Differentiation of 3T3-F442A Preadipocytes.

P. de Mazancourt, Y. Giudicelli, M. Morot, 1998, Endocrinology.

G proteins in adipocytes and preadipocytes: characterization, subcellular distribution, and potential roles for Gi2 and/or Gi3 in the control of cell proliferation.

P. de Mazancourt, Y. Giudicelli, P. Goldsmith, 1996, Cellular signalling.

Adiponectin promotes syncytialisation of BeWo cell line and primary trophoblast cells

P. de Mazancourt, M. Dieudonné, M. Leneveu, 2010, Reproductive biology and endocrinology : RB&E.

Adiponectin and leptin systems in human endometrium during window of implantation.

P. de Mazancourt, M. Dieudonné, E. Dos Santos, 2012, Fertility and sterility.

Hypoxia-inducible factor 1 controls the expression of the uncoordinated-5-B receptor, but not of netrin-1, in first trimester human placenta.

P. de Mazancourt, N. Alfaidy, V. Studer, 2011, The International journal of developmental biology.

Antiproliferative and proapoptotic effects of bisphenol A on human trophoblastic JEG-3 cells.

P. de Mazancourt, M. Dieudonné, E. Dos Santos, 2011, Reproductive toxicology.

Involvement of estrogen-related receptor-γ and mitochondrial content in intrauterine growth restriction and preeclampsia.

P. de Mazancourt, M. Dieudonné, E. Dos Santos, 2015, Fertility and sterility.

Does glucocorticoid deprivation promote the expression of adenosine receptor-sites stimulating adenylate cyclase in rat adipocyte membranes?

P. de Mazancourt, Y. Giudicelli, N. R. Thotakura, 1982, Biochemical and biophysical research communications.

Two novel fibrinogen variants found in patients with pulmonary embolism and their families

P. de Mazancourt, M. Dechavanne, M. Hanss, 2003, Journal of thrombosis and haemostasis : JTH.

Semi-quantitative RT-PCR for comparison of mRNAs in cells with different amounts of housekeeping gene transcripts.

P. de Mazancourt, Y. Giudicelli, V. Serazin-Leroy, 1998, Molecular and cellular probes.

A Simple RFLP-Based Method for HFE Gene Multiplex Amplification and Determination of Hereditary Hemochromatosis-Causing Mutation C282Y and H63D Variant with Highly Sensitive Determination of Contamination

P. de Mazancourt, J. Rabès, Ludmilla OGOUMA-AWORET, 2020, BioMed research international.

X‐chromosome inactivation in female patients with Fabry disease

A. Hagège, P. de Mazancourt, O. Dubourg, 2016, Clinical genetics.

Rapid and sensitive high-performance liquid chromatographic method for simultaneous determination of retinol, alpha-tocopherol, 25-hydroxyvitamin D3 and 25-hydroxyvitamin D2 in human plasma with photodiode-array ultraviolet detection.

P. de Mazancourt, J. Alvarez, P. D. Mazancourt, 2001, Journal of chromatography. B, Biomedical sciences and applications.

Structural analysis of the impact of a novel androgen receptor gene mutation in two adult patients with mild androgen insensitivity syndrome

S. Mercier, P. de Mazancourt, Y. Péréon, 2020, Andrologia.

Different sensitivity of von Clauss reagents for the diagnosis of dysfibrinogenemia

P. de Mazancourt, M. Vasse, P. van Dreden, 2019, European journal of haematology.

Guanine nucleotide‐ and GTP‐dependent N6‐phenylisopropyladenosine stimulation of the membrane‐bound cyclic AMP high affinity phosphodiesterase in rat brain

P. de Mazancourt, Y. Giudicelli, 1984, FEBS letters.

Guanine nucleotides and adenosine ‘Ri’‐site analogues stimulate the membrane‐bound low‐K m cyclic AMP phosphodiesterase of rat adipocytes

P. de Mazancourt, Y. Giudicelli, 1984, FEBS letters.

An unusual clinical presentation of factor XIII deficiency and issues relating to the monitoring of factor XIII replacement therapy

P. de Mazancourt, C. Négrier, P. Gaucherand, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Prolactin treatment increases GLUT2 but not the G protein subunit content in cell membranes from cultured neonatal rat islets

P. de Mazancourt, A. Boschero, E. Carneiro, 1994, FEBS letters.

Evidence for a defect in the number of beta-adrenergic receptors and in the adenylate cyclase responsiveness to guanine nucleotides in fat cells after adrenalectomy.

P. de Mazancourt, Y. Giudicelli, N. R. Thotakura, 1982, Biochimica et biophysica acta.

Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) Programs

P. de Mazancourt, E. Dos Santos, F. Vialard, 2014, PloS one.

P. de Mazancourt, M. Dieudonné, E. Dos Santos, 2012, Placenta.

A comparative study of two methods of dental pulp extraction for genetic fingerprinting.

P. de Mazancourt, F. Tilotta, P. Brousseau, 2010, Forensic science international.

TWEAK Appears as a Modulator of Endometrial IL-18 Related Cytotoxic Activity of Uterine Natural Killers

J. Foidart, C. Munaut, P. de Mazancourt, 2011, PloS one.

Tumor necrosis factor-like weak inducer of apoptosis (TWEAK)/fibroblast growth factor inducible-14 might regulate the effects of interleukin 18 and 15 in the human endometrium.

P. de Mazancourt, V. Sérazin, G. Chaouat, 2010, Fertility and sterility.

Prothrombin Suresnes: a case of homozygous F299V mutation responsible for hypodysprothrombinemia.

P. de Mazancourt, D. François, D. Vignon, 2006, Haematologica.

The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (AαCys36Gly, AαCys36Arg and AαCys45Tyr) confirms the role of N-terminal Aα disulfide bonds in protein assembly and secretion

P. Morange, P. de Mazancourt, J. Abgrall, 2011, Haematologica.

High level expression of transfected G protein αi3 subunit is required for plasma membrane targeting and adenylyl cyclase inhibition in NIH 3T3 fibroblasts

S. Hermouet, P. de Mazancourt, M. Farquhar, 1992 .

Y-STR DNA amplification as biological evidence in sexually assaulted female victims with no cytological detection of spermatozoa.

P. de Mazancourt, M. Durigon, G. Lorin de la Grandmaison, 2002, Forensic science international.

Rat preadipocyte adenylyl cyclase: influence of fat localization and androgenic status.

P. de Mazancourt, Y. Giudicelli, D. Lacasa, 1994, Biochimica et biophysica acta.

A Bβ 14 Arg → Cys fibrinogen variant in a patient with thrombotic complications (fibrinogen St‐Germain III)

P. de Mazancourt, E. de Raucourt, G. Meyer, 2006, Journal of thrombosis and haemostasis : JTH.

The 'relics of Joan of Arc': a forensic multidisciplinary analysis.

E. Willerslev, P. de Mazancourt, J. Poupon, 2010, Forensic science international.

Morphine and 6-acetylmorphine concentrations in blood, brain, spinal cord, bone marrow and bone after lethal acute or chronic diacetylmorphine administration to mice.

P. de Mazancourt, J. Alvarez, M. Durigon, 2007, Forensic science international.

Skeletal remains presumed submerged in water for three years identified using PCR-STR analysis.

P. de Mazancourt, M. Durigon, M. Leterreux, 2002, Journal of forensic sciences.

A High‐Performance Liquid Chromatography Method with Photodiode‐Array UV Detection for Therapeutic Drug Monitoring of the Nontricyclic Antidepressant Drugs

P. de Mazancourt, J. Alvarez, G. L. de la Grandmaison, 2003, Therapeutic drug monitoring.

A case of lethal hypophosphatasia providing new insights into the perinatal benign form of hypophosphatasia and expression of the ALPL gene

P. de Mazancourt, I. Brun-Heath, E. Mornet, 2007, Clinical genetics.

A rapid and sensitive high-performance liquid chromatography method for determination of embutramide (a Tanax or T61 component) in human blood with photodiode-array UV detection.

B. Mathieu, P. de Mazancourt, J. Alvarez, 2004, Journal of analytical toxicology.

Simultaneous determination of thirteen beta-blockers and one metabolite by gradient high-performance liquid chromatography with photodiode-array UV detection.

P. de Mazancourt, J. Alvarez, Magali Delamoye, 2004, Forensic science international.

Genome wide expression profile in human HTR-8/Svneo trophoblastic cells in response to overexpression of placental alkaline phosphatase gene.

P. de Mazancourt, M. Dieudonné, G. Meurice, 2011, Placenta.

A sequence variation in the promoter of the placental alkaline phosphatase gene (ALPP) is associated with allele-specific expression in human term placenta.

P. de Mazancourt, M. Dieudonné, I. Brun-Heath, 2010, Placenta.

A simplified method for the detection of Y chromosome microdeletions in infertile men using a multiplex sequence-tagged site-based amplification.

C. Boucly, B. Mathieu, P. de Mazancourt, 2002, Genetic testing.

Case report: Meiotic segregation in spermatozoa of a 46,X,t(Y;10)(q11.2;p15.2) fertile translocation carrier.

J. Roume, P. de Mazancourt, F. Vialard, 2009, Reproductive biomedicine online.

Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles

P. de Mazancourt, I. Brun-Heath, D. Fauvert, 2009, BMC Medical Genetics.

Childhood hypophosphatasia due to a de novo missense mutation in the tissue-nonspecific alkaline phosphatase gene.

P. de Mazancourt, I. Brun-Heath, E. Mornet, 2005, The Journal of clinical endocrinology and metabolism.

Preimplantation Factor (PIF) Promotes Human Trophoblast Invasion1

P. de Mazancourt, M. Dieudonné, F. Vialard, 2014, Biology of reproduction.

Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.

E. Chouery, A. Mégarbané, P. de Mazancourt, 2007, American journal of human genetics.

Array Comparative Genomic Hybridization in Prenatal Diagnosis: Another Experience

J. Roume, P. de Mazancourt, V. Sérazin, 2009, Fetal Diagnosis and Therapy.

Characterization and Expression of Netrin-1 and Its Receptors UNC5B and DCC in Human Placenta

P. de Mazancourt, Y. Giudicelli, M. Dakouane-Giudicelli, 2010, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Inhibition of human placental endothelial cell proliferation and angiogenesis by netrin-4.

S. Brouillet, P. de Mazancourt, N. Alfaidy, 2015, Placenta.

Use of Genotypic Identification by sodA Sequencing in a Prospective Study To Examine the Distribution of Coagulase-Negative Staphylococcus Species among Strains Recovered during Septic Orthopedic Surgery and Evaluate Their Significance

P. de Mazancourt, P. Trieu-Cuot, J. Gaillard, 2005, Journal of Clinical Microbiology.

Use of sodA sequencing for the identification of clinical isolates of coagulase-negative staphylococci.

P. de Mazancourt, P. Trieu-Cuot, J. Gaillard, 2004, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

Fibrinogen Poissy II (&ggr;N361K): a novel dysfibrinogenemia associated with defective polymerization and peptide B release

P. de Mazancourt, Y. Giudicelli, J. Alvarez, 2003, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

P. de Mazancourt, P. Calès, S. Michalak, 2007, Journal of thrombosis and haemostasis : JTH.

Fibrinogen Saint-Germain II: Hypofibrinogenemia due to heterozygous γ N345S mutation

P. de Mazancourt, E. de Raucourt, S. Brennan, 2005, Thrombosis and Haemostasis.

A new electrophoretic variant of fibrinogen associated with venous thromboembolism, fibrinogen Bordeaux Aα Arg439→Cys

C. Vergnes, P. de Mazancourt, M. Hanss, 2008, Journal of thrombosis and haemostasis : JTH.

DNA analysis using an integrated microchip for multiplex PCR amplification and electrophoresis for reference samples.

James P Landers, Luc Chassagne, Brian E Root, 2014, Analytical chemistry.

A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy.

P. Gejman, P. de Mazancourt, L. Weinstein, 1992, Genomics.

A novel LC-ESI-MS-MS method for sensitive quantification of colchicine in human plasma: application to two case reports.

P. de Mazancourt, J. Alvarez, I. Etting, 2006, Journal of analytical toxicology.

Study of the diagnostic value of iron in fresh water drowning.

P. de Mazancourt, J. Alvarez, M. Durigon, 2006, Forensic science international.

Role of factor VIII on activated protein C resistance ratio in inflammatory diseases

P. de Mazancourt, Y. Giudicelli, M. Denninger, 1996, British journal of haematology.

Inhibition of adenylate cyclase activity by galanin in rat insulinoma cells is mediated by the G-protein Gi3.

P. de Mazancourt, L. Weinstein, P. Goldsmith, 1994, The Biochemical journal.

Multiplex amplification of mitochondrial DNA for human and species identification in forensic evaluation.

P. de Mazancourt, M. Durigon, M. Leterreux, 1999, Forensic science international.

Severe prekallikrein deficiencies due to homozygous C529Y mutations.

P. de Mazancourt, M. Horellou, J. Conard, 2007, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Recurrent thromboembolism in a patient with beta-thalassemia major associated with double heterozygosity for factor V R506Q and prothrombin G20210A mutations.

P. de Mazancourt, E. de Raucourt, C. Veyssier-Belot, 2002, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Netrins and Their Roles in Placental Angiogenesis

P. de Mazancourt, N. Alfaidy, M. Dakouane-Giudicelli, 2014, BioMed research international.

Partial atlE Sequencing of Staphylococcus epidermidis Strains from Prosthetic Joint Infections

M. Le Moal, P. de Mazancourt, P. Hoffmeyer, 2009, Journal of Clinical Microbiology.

Successful Pregnancy under Fibrinogen Substitution with Heparin and Aspirin in a Woman with Dysfibrinogenemia Revealed by Placental Abruption

J. Gris, P. de Mazancourt, M. Hanss, 2018, Thrombosis and Haemostasis.

Characterization of combined factor VII and factor XI deficiencies

P. de Mazancourt, E. de Raucourt, F. Quélin, 2008, Haemophilia.

Prospective analysis of factor XI deficiencies in the Marseilles area identified four novel mutations among 12 consecutive unrelated families

P. Morange, P. de Mazancourt, C. Frère, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Trophoblast syncytialisation necessitates mitochondrial function through estrogen-related receptor-γ activation.

P. de Mazancourt, M. Dieudonné, E. Dos Santos, 2015, Molecular human reproduction.

EG-VEGF controls placental growth and survival in normal and pathological pregnancies: case of fetal growth restriction (FGR)

S. Brouillet, P. de Mazancourt, M. Dieudonné, 2012, Cellular and Molecular Life Sciences.

Netrins and Their Roles in Placental Angiogenesis

P. de Mazancourt, N. Alfaidy, M. Dakouane-Giudicelli, 2014, BioMed Research International.

Effects of 17beta-estradiol on preadipocyte proliferation in human adipose tissue: Involvement of IGF1-R signaling.

B. Mignotte, P. de Mazancourt, M. Dieudonné, 2010, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Fibrinogen Paris IX: a case of symptomatic hypofibrinogenemia with Bβ Y236C and Bβ IVS7‐1G→C mutations

P. de Mazancourt, J. Conard, V. Mathieux, 2006, Journal of thrombosis and haemostasis : JTH.

Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders

P. de Mazancourt, C. Biron-Andréani, E. de Raucourt, 2023, European journal of haematology.

Is primary prophylaxis required in afibrinogenemia?

P. de Mazancourt, V. Gay, B. Polack, 2010, Transfusion.

Forensic and police identification of "X" bodies. A 6-years French experience.

P. de Mazancourt, P. Charlier, G. L. de la Grandmaison, 2011, Forensic science international.

Functional Fibrinolysis Assays Reveal Different Mechanisms underlying Plasminogen Dysfunction in Ligneous Conjunctivitis

P. de Mazancourt, E. de Raucourt, B. Ho-Tin-Noé, 2020, Thrombosis and Haemostasis.

Fibrinogen Saint-Germain I: a case of the heterozygous Aα GLY 12 → VAL fibrinogen variant

P. de Mazancourt, E. de Raucourt, J. Alvarez, 2002, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Allele frequencies and haplotypes of eight Y-short tandem repeats in Bantu population living in Central Africa.

M. Lecerf, P. de Mazancourt, L. Bélec, 2007, Forensic science international.

Molecular characterization of a novel mutation in the factor XIII a subunit gene associated with a severe defect: importance of prophylactic substitution.

P. Morange, C. Boucly, P. de Mazancourt, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Molecular characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis

P. Morange, P. de Mazancourt, C. Frère, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

Drug stability testing to support clinical feasibility investigations for intrathecal baclofen-clonidine admixture.

P. de Mazancourt, E. Chartier-Kastler, P. Denys, 2004, Journal of pain and symptom management.

Next Generation Sequencing and Association Studies in Familial Nonmedullary Thyroid Carcinoma: Let’s Choose Appropriate Controls

P. de Mazancourt, L. Groussin, J. Ropers, 2017, European Thyroid Journal.

A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder

R. Carlier, P. de Mazancourt, K. Bénistan, 2021, Clinical case reports.

Classical Ehlers–Danlos syndrome with severe kyphoscoliosis due to a novel pathogenic variant of COL5A2

R. Carlier, P. de Mazancourt, K. Bénistan, 2022, Clinical case reports.

A severe case of PLOD1 ‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report

X. Jeunemaître, P. de Mazancourt, K. Bénistan, 2023, Clinical case reports.

Four novel FXI gene mutations in three factor XI- deficient patients

P. de Mazancourt, E. de Raucourt, F. Quélin, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Liquid chromatography/photodiode array detection for determination of strychnine in blood: a fatal case report.

P. de Mazancourt, J. Alvarez, G. L. de la Grandmaison, 2004, Forensic science international.

Polymorphism of the Cell Wall-Anchoring Domain of the Autolysin-Adhesin AtlE and Its Relationship to Sequence Type, as Revealed by Multilocus Sequence Typing of Invasive and Commensal Staphylococcus epidermidis Strains

P. de Mazancourt, J. Gaillard, P. Piriou, 2006, Journal of Clinical Microbiology.

A case of afibrinogenemia associated with A-alpha chain gene compound heterozygosity (HUMFIBRA c.[4110delA]+[3200+1G>T])

P. de Mazancourt, S. Claeyssens, M. Dreyfus, 2007, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K).

P. de Mazancourt, E. de Raucourt, B. Guillet, 2005, Haematologica.

The high frequency of sperm aneuploidy in klinefelter patients and in nonobstructive azoospermia is due to meiotic errors in euploid spermatocytes.

P. de Mazancourt, F. Vialard, J. Selva, 2012, Journal of andrology.

Differential modulation of the adenylate cyclase/cyclic AMP stimulatory pathway by protein kinase C activation in rat adipose tissue and isolated fat cells. Influence of collagenase digestion.

C. Darimont, P. de Mazancourt, J. Giot, 1991, Biochemical pharmacology.

A comparative study of two methods of dental pulp extraction for genetic fingerprinting.

P. de Mazancourt, F. Tilotta, P. Brousseau, 2010, Forensic Science International.

A focus on dominant negative variants in a series of 170 heterozygous FXI‐deficient patients

P. de Mazancourt, C. Biron-Andréani, E. de Raucourt, 2023, Haemophilia : the official journal of the World Federation of Hemophilia.

Reinvestigation of unidentified causative variants in FXI‐deficient patients: Focus on gene segment deletions

P. de Mazancourt, A. Harroche, S. Castet, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.