A. Aissat

发表

Resveratrol rescues cAMP‐dependent anionic transport in the cystic fibrosis pancreatic cell line CFPAC1

A. Edelman, N. Hamdaoui, J. Fritsch, 2011, British journal of pharmacology.

Acquired spherocytosis due to somatic ANK1 mutations as a manifestation of clonal hematopoiesis in elderly patients

L. Garçon, B. Funalot, I. Radford‐Weiss, 2022, American journal of hematology.

Exome sequencing for diagnosis of congenital hemolytic anemia

N. Costedoat-Chalumeau, B. Funalot, F. Galactéros, 2020, Orphanet Journal of Rare Diseases.

Transcriptomic Signature of the CD24hiCD38hi Transitional B Cells Associated With an Immunoregulatory Phenotype in Renal Transplant Recipients

F. Pirenne, P. Grimbert, J. Cohen, 2016, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Targeting p16INK4a Promotes Lipofibroblasts and Alveolar Regeneration After Early Life Injury.

J. Tran van Nhieu, R. Epaud, M. Zysman, 2020, American journal of respiratory and critical care medicine.

COMMD1 modulates noxious inflammation in cystic fibrosis.

S. Moutéreau, A. Hinzpeter, S. le Gouvello, 2013, The international journal of biochemistry & cell biology.

Alternative Splicing of In‐Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies

L. Galietta, E. Girodon, E. Bieth, 2013, Human mutation.

New use for an old drug: COX‐independent anti‐inflammatory effects of sulindac in models of cystic fibrosis

R. Epaud, A. Hulin, S. Manin, 2016, British journal of pharmacology.

Phosphorylation of the Chaperone-Like HspB5 Rescues Trafficking and Function of F508del-CFTR

S. Simon, D. Rotin, X. Decrouy, 2020, International journal of molecular sciences.

Absolute and relative rate constants for the reactions of OH and Cl with pentanols

A. Mellouki, M. Cazaunau, V. Daële, 2013 .

Methylprednisolone pulse treatment improves ProSP‐C trafficking in twins with SFTPC mutation: An isoform story?

S. Simon, S. Finet, R. Epaud, 2020, British journal of clinical pharmacology.

Interstitial lung disease reveals 48,XXYY syndrome in a child

R. Epaud, B. Funalot, A. Aissat, 2019, Acta paediatrica.

Th‐17 Alloimmune Responses in Renal Allograft Biopsies From Recipients of Kidney Transplants Using Extended Criteria Donors During Acute T Cell–Mediated Rejection

P. Grimbert, P. Rémy, D. Saadoun, 2015, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Prenatal Ultrasound Suspicion of Cystic Fibrosis in a Multiethnic Population: Is Extensive CFTR Genotyping Needed?

B. Funalot, S. Whalen, V. Mirlesse, 2021, Genes.

Combined Computational–Experimental Analyses of CFTR Exon Strength Uncover Predictability of Exon‐Skipping Level

E. Girodon, C. Vasseur, M. Goossens, 2013, Human mutation.

Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation

G. Bouyer, L. Garçon, L. Kiger, 2021, American journal of hematology.

Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype

S. Simon, R. Epaud, X. Decrouy, 2017, European Journal of Human Genetics.

A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practice.

M. Claustres, R. Epaud, E. Girodon, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

COMMD1-Mediated Ubiquitination Regulates CFTR Trafficking

M. Goossens, N. Arous, A. Hinzpeter, 2011, PloS one.