Marie-Paule Algros

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Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.

Sophie Valleix, Florence Niel, +5 authors Bernadette Kantelip
American journal of human genetics
2006

Congenital primary aphakia (CPA) is a rare developmental disorder characterized by the absence of lens, the development of which is normally induced during the 4th-5th wk of human embryogenesis. This… (More)

Discordances in Estrogen Receptor Status, Progesterone Receptor Status, and HER2 Status Between Primary Breast Cancer and Metastasis

Elsa Curtit, Virginie Nerich, +9 authors Xavier Pivot
The oncologist
2013

BACKGROUND The primary aim of this retrospective study was to investigate intraindividual correlation of estrogen receptor (ER) status, progesterone receptor (PR) status, and HER2 status between… (More)

Expression of E-cadherin and alpha-, beta-, gamma-catenins in patients with bladder cancer: identification of gamma-catenin as a new prognostic marker of neoplastic progression in T1 superficial…

Anne Clairotte, Isabelle Lascombe, +5 authors Bernadette Kantelip
American journal of clinical pathology
2006

Loss of intercellular adhesion facilitates tumor invasion. To clarify the relation between altered expression of cell adhesion molecules and progression of T1 superficial bladder tumors, 101 cases… (More)

The autophagy GABARAPL1 gene is epigenetically regulated in breast cancer models

Eric Hervouet, Aurore Claude-Taupin, +9 authors Michaël Boyer-Guittaut
BMC Cancer
2015

The GABARAP family members (GABARAP, GABARAPL1/GEC1 and GABARAPL2 /GATE-16) are involved in the intracellular transport of receptors and the autophagy pathway. We previously reported that GABARAPL1… (More)

Relevance of p185 HER-2/neu oncoprotein quantification in human primary breast carcinoma

Laurent Bermont, Marie-Paule Algros, M Baron, Gérard L. Adessi
Breast Cancer Research and Treatment
2000

The c-erbB-2 proto-oncogene encodes a transmembrane protein tyrosine kinase receptor of 185 kDa (p185) and has been associated with several types of human cancers. In human breast cancer,… (More)

Expression of E-Cadherin and α-, β-, γ-Catenins in Patients With Bladder Cancer Identification of γ-Catenin as a New Prognostic Marker of Neoplastic Progression in T 1 Superficial Urothelial Tumors

Anne Clairotte, Isabelle Lascombe, +5 authors Bernadette Kantelip
2005

Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.

Nadine Magy, Sophie Valleix, +5 authors J. L. Dupond
Amyloid : the international journal of…
2002

A French family in which three individuals had familial amyloid polyneuropathy (FAP) was investigated. The proband presented cardiomyopathy with atrial arrhythmia and then developed axonal… (More)

[Familial infantile myofibromatosis].

Eve Puzenat, Stamatina Marioli, +5 authors François Aubin
Annales de dermatologie et de venereologie
2009

BACKGROUND Infantile myofibromatosis (IM) is the most common fibrous disorder of infancy and childhood. It is characterized by congenital tumours of the skin, striated muscle, bones and viscera. Most… (More)

[Economic assessment of the routine use of Oncotype DX® assay for early breast cancer in Franche-Comte region].

Virginie Nerich, Elsa Curtit, +13 authors Xavier Pivot
Bulletin du cancer
2014

Oncotype DX® has been validated as quantifying the likelihood of distant recurrence at 10 years and overall chemotherapy benefit in patients with estrogen-receptor-positive and HER-2-negative early… (More)

[Small intestinal stromal tumors with skenoid fibers. Clinicopathological study of three cases].

Marie-Paule Algros, Frédéric Ringenbach, Gabriel Viennet, P-O Denue, Bernadette Kantelip, Georges André Mantion
Annales de chirurgie
2003

Gastrointestinal stromal tumours (Gist) are mesenchymal tumour with uncertain prognosis occurring in the gastrointestinal tract wall. For clinicians, these tumours raise two problems: to establish… (More)

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