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pro vyhledávání: '"Christine, Petit"'
Autor:
Davis, Tinsley H.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2017 Aug 01. 114(31), 8132-8134.
Externí odkaz:
https://www.jstor.org/stable/26487178
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hajer Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, CRYSTEL Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/d1f20ca9f1e041b5805610de30e16616
Autor:
Christine Petit
Les travaux de Christine Petit sur l’audition et la surdité héréditaire, de portée majeure pour les jeunes malentendants, devraient aussi améliorer la vie des seniors. La cochlée, organe sensoriel de l’audition, n’a plus de secret – ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::577a68ba8c308d0a1ac9ad2b54cee131
http://journals.openedition.org/lettre-cdf/3062
http://journals.openedition.org/lettre-cdf/3062
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hager Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, Crystel Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic etiologies. In Tunisia, HI underdiagnosis prevails, primarily due to limited access to com
Externí odkaz:
https://doaj.org/article/d53f3da42b5b4e8f9503ec02796dd375
Autor:
PETIT, CHRISTINE
Publikováno v:
Fonction Crédit Magazine. 2023, Issue 93, p70-71. 2p.
Le Prix Kavli, prix international en neurosciences de l’Académie norvégienne des sciences et des lettres a été décerné en 2018 à Christine Petit, professeur titulaire de la chaire Génétique et physiologie cellulaire. Il récompense son «
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=openedition_::9dd3fe44c513ef78c5dede6b8602fd62
http://journals.openedition.org/lettre-cdf/4425
http://journals.openedition.org/lettre-cdf/4425
Autor:
Frank Zimmermann
Publikováno v:
Physical Review Special Topics. Accelerators and Beams, Vol 16, Iss 5, p 050001 (2013)
Externí odkaz:
https://doaj.org/article/aa2b3c2048bd432b893baa8f9ebad112
Akademický článek
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Autor:
Tinsley H. Davis
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 114(31)
Over the last 20 years, geneticist and neurobiologist Christine Petit has written the canticle of the cochlea from scratch, revealing the long-shrouded machinery of the auditory system molecule by molecule. Along the way, she has identified more than
Autor:
Christine Petit
Publikováno v:
La lettre du Collège de France. :79
Christine Petit’s work on hearing and hereditary deafness, of major importance for hearing-impaired young people, should also improve the life of the elderly. The cochlea, the sensory organ of hearing, is virtually an open book for Christine Petit,