Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Gène homéotique")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 765

  • Page / 31
Export

Selection :

  • and

The rx-like homeobox gene (Rx-L) is necessary for normal photoreceptor developmentYI PAN; NEKKALAPUDI, Srivamsi; KELLY, Lisa E et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 10, pp 4245-4253, issn 0146-0404, 9 p.Article

Developmental evolution: new paradigms and paradoxesWRAY, G. A.Developmental genetics. 1994, Vol 15, Num 1, pp 1-6, issn 0192-253XArticle

Assignment of the human homologue of the Drosophila cut homoebox gene (CUTL1) to band 7q22 by fluorescence in situ hybridizationLEMIEUX, N; XIAO-XIANG ZHANG; DUFORT, D et al.Genomics (San Diego, Calif.). 1994, Vol 24, Num 1, pp 191-193, issn 0888-7543Article

Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular SyndromeSCHORDERET, Daniel F; NICHINI, Olivia; BOISSET, Gaëlle et al.American journal of human genetics. 2008, Vol 82, Num 5, pp 1178-1184, issn 0002-9297, 7 p.Article

BNP is a transcriptional target of the short stature homeobox gene SHOXMARCHINI, Antonio; HÄCKER, Beate; MARTTILA, Tiina et al.Human molecular genetics (Print). 2007, Vol 16, Num 24, pp 3081-3087, issn 0964-6906, 7 p.Article

Role of homeobox genes in normal mammary gland development and breast tumorigenesisHEXIN CHEN; SUKUMAR, Saraswati.Journal of mammary gland biology and neoplasia. 2003, Vol 8, Num 2, pp 159-175, issn 1083-3021, 17 p.Article

NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significanceBALLERINI, P; BUSSON, M; FASOLA, S et al.Leukemia. 2005, Vol 19, Num 3, pp 468-470, issn 0887-6924, 3 p.Article

The genesis and evolution of homeobox gene clustersGARCIA-FERNANDEZ, Jordi.Nature reviews. Genetics (Print). 2005, Vol 6, Num 12, pp 881-892, issn 1471-0056, 12 p.Article

The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retinaREICHMAN, Sacha; REDDY KALATHUR, Ravi Kiran; LEVEILLARD, Thierry et al.Human molecular genetics (Print). 2010, Vol 19, Num 2, pp 250-261, issn 0964-6906, 12 p.Article

Expression of the homeobox gene Pitx2 in neural crest is required for optic stalk and ocular anterior segment developmentEVANS, Amanda L; GAGE, Philip J.Human molecular genetics (Print). 2005, Vol 14, Num 22, pp 3347-3359, issn 0964-6906, 13 p.Article

Assignment1 of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mappingLEE-KIRSCH, M. A; ENGEL, K; PADITZ, E et al.Cytogenetics and cell genetics. 2001, Vol 92, Num 3-4, issn 0301-0171, p. 358Article

Gènes sélecteurs, identité des membres et latéralité chez les vertébrés : Développement et Évolution = Selector genes, limb identity and laterality in vertebrates : Development and EvolutionDROUIN, J.MS. Médecine sciences. 2000, Vol 16, Num 2, pp 181-185, issn 0767-0974Article

Assignment of SHOX2 (alias OG12x and SHOT) to human chromosome bands 3q25→q26.1 by in situ hybridizationDE BAERE, E; SPELEMAN, F; VAN ROY, N et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 3-4, pp 228-229, issn 0301-0171Article

A rational nomenclature for vertebrate homeobox (HOX) genesSCOTT, M. P.Nucleic acids research. 1993, Vol 21, Num 8, pp 1687-1688, issn 0305-1048Article

Tissu conjonctif de soutien et genèse des prolapsus = Connecrive tissue and prolapse genesisTREMOLLIERES, F.Gynécologie obstétrique & fertilité. 2010, Vol 38, Num 6, pp 388-393, issn 1297-9589, 6 p.Article

CDX2, a homeobox transcription factor, upregulates transcription of the p21/WAF1/CIP1 geneBAI, Yun-Qing; MIYAKE, Satoshi; IWAI, Takehisa et al.Oncogene (Basingstoke). 2003, Vol 22, Num 39, pp 7942-7949, issn 0950-9232, 8 p.Article

Vertebrate evolution: recent perspectives from fishAPARICIO, S.Trends in genetics (Regular ed.). 2000, Vol 16, Num 2, pp 54-56, issn 0168-9525Article

Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndromeLE GOFF, Carine; MAHAUT, Clémentine; MARLIN, Sandrine et al.Nature genetics. 2012, Vol 44, Num 1, pp 85-88, issn 1061-4036, 4 p.Article

HOMEOTIC MUTANTS AND THE ASSIMILATION OF DEVELOPMENTAL GENETICS INTO THE EVOLUTIONARY SYNTHESIS, 1915―1952 = Les mutants homéotiques et l'assimilation de la génétique du développement dans la théorie synthétique de l'évolution, 1915-1952DAVIS, Gregory K; DIETRICH, Michael R; JACOBS, David K et al.Transactions of the American philosophical society. 2009, Vol 99, Num 1, pp 133-154, issn 0065-9746, 22 p.Conference Paper

Préadaptation et biologie moléculaire : Vers un renouveau du concept ? = Preadaptation and molecular biology : a move towards a renewal of the concept ?LE GUYADER, H.Bulletin de la Société zoologique de France. 1996, Vol 121, Num 1, pp 39-44, issn 0037-962XConference Paper

Dinucleotide repeat polymorphism at the TENS and SCHOX1 loci in chickenKHATIB, H; SOLLER, M.Animal genetics (Print). 1994, Vol 25, Num 3, issn 0268-9146, p. 199Article

Localization of the OTF3 gene within the human MHC class I region by physical and meiotic mappingCROUAU-ROY, B; AMADOU, C; BOUISSOU, C et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 1, pp 241-243, issn 0888-7543Article

Deciphering the Hox code : clues to patterning branchial regions of the headHUNT, P; KRUMIAUF, R.Cell (Cambridge). 1991, Vol 66, Num 6, pp 1075-1078, issn 0092-8674Article

Eleven daughters of NANOGBOOTH, H. Anne F; HOLLAND, Peter W. H.Genomics (San Diego, Calif.). 2004, Vol 84, Num 2, pp 229-238, issn 0888-7543, 10 p.Article

Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1-p21.3GRIGORIOU, M; KASTRINAKI, M.-C; MODI, W. S et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 3, pp 550-555, issn 0888-7543Article

  • Page / 31