Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1980 1
1981 3
1982 2
1983 4
1985 2
1986 1
1988 1
1990 1
1991 1
1993 2
1998 1
2001 1
2003 1
2005 1
2007 1
2008 1
2009 1
2013 1
2014 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

28 results

Results by year

Filters applied: . Clear all
Page 1
Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.
Jaglin XH, Poirier K, Saillour Y, Buhler E, Tian G, Bahi-Buisson N, Fallet-Bianco C, Phan-Dinh-Tuy F, Kong XP, Bomont P, Castelnau-Ptakhine L, Odent S, Loget P, Kossorotoff M, Snoeck I, Plessis G, Parent P, Beldjord C, Cardoso C, Represa A, Flint J, Keays DA, Cowan NJ, Chelly J. Jaglin XH, et al. Among authors: phan dinh tuy f. Nat Genet. 2009 Jun;41(6):746-52. doi: 10.1038/ng.380. Epub 2009 May 24. Nat Genet. 2009. PMID: 19465910 Free PMC article.
Deficit of suppressor T cells in active multiple sclerosis.
Bach MA, Phan-Dinh-Tuy F, Tournier E, Chatenoud L, Bach JF, Martin C, Degos JD. Bach MA, et al. Among authors: phan dinh tuy f. Lancet. 1980 Dec 6;2(8206):1221-3. doi: 10.1016/s0140-6736(80)92480-0. Lancet. 1980. PMID: 6108395
Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate.
Laumonnier F, Holbert S, Ronce N, Faravelli F, Lenzner S, Schwartz CE, Lespinasse J, Van Esch H, Lacombe D, Goizet C, Phan-Dinh Tuy F, van Bokhoven H, Fryns JP, Chelly J, Ropers HH, Moraine C, Hamel BC, Briault S. Laumonnier F, et al. Among authors: phan dinh tuy f. J Med Genet. 2005 Oct;42(10):780-6. doi: 10.1136/jmg.2004.029439. J Med Genet. 2005. PMID: 16199551 Free PMC article.
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes.
Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Phan Dinh Tuy F, Chelly J, Morris HD, Riegler J, Lythgoe MF, Arkell RM, Loreni F, Flint J, Pavan WJ, Keays DA. Watkins-Chow DE, et al. Among authors: phan dinh tuy f. PLoS Genet. 2013;9(1):e1003094. doi: 10.1371/journal.pgen.1003094. Epub 2013 Jan 31. PLoS Genet. 2013. PMID: 23382688 Free PMC article.
Protein kinases in normal human blood cells.
Phan Dinh Tuy F, Henry J, Rosenfeld C, Kahn A. Phan Dinh Tuy F, et al. Am J Hematol. 1983 Sep;15(2):105-15. doi: 10.1002/ajh.2830150202. Am J Hematol. 1983. PMID: 6613983
Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus.
Nosten-Bertrand M, Kappeler C, Dinocourt C, Denis C, Germain J, Phan Dinh Tuy F, Verstraeten S, Alvarez C, Métin C, Chelly J, Giros B, Miles R, Depaulis A, Francis F. Nosten-Bertrand M, et al. Among authors: phan dinh tuy f. PLoS One. 2008 Jun 25;3(6):e2473. doi: 10.1371/journal.pone.0002473. PLoS One. 2008. PMID: 18575605 Free PMC article.
Protein kinases in human leukemic cells.
Phan-Dinh-Tuy F, Henry J, Boucheix C, Perrot JY, Rosenfeld C, Kahn A. Phan-Dinh-Tuy F, et al. Am J Hematol. 1985 Jul;19(3):209-18. doi: 10.1002/ajh.2830190302. Am J Hematol. 1985. PMID: 3860003
Characterization of human red blood cell tyrosine kinase.
Phan-Dinh-Tuy F, Henry J, Kahn A. Phan-Dinh-Tuy F, et al. Biochem Biophys Res Commun. 1985 Jan 16;126(1):304-12. doi: 10.1016/0006-291x(85)90606-0. Biochem Biophys Res Commun. 1985. PMID: 3882086
Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency.
Kappeler C, Dhenain M, Phan Dinh Tuy F, Saillour Y, Marty S, Fallet-Bianco C, Souville I, Souil E, Pinard JM, Meyer G, Encha-Razavi F, Volk A, Beldjord C, Chelly J, Francis F. Kappeler C, et al. Among authors: phan dinh tuy f. J Comp Neurol. 2007 Jan 10;500(2):239-54. doi: 10.1002/cne.21170. J Comp Neurol. 2007. PMID: 17111359
28 results