Ottolenghi C - Search Results

1

The INSL4 gene maps close to WI-5527 at 9p24.1-->p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome.

Veitia R, Laurent A, Quintana-Murci L, Ottolenghi C, Fellous M, Vidaud M, McElreavey K. Veitia R, et al. Among authors: ottolenghi c. Cytogenet Cell Genet. 1998;81(3-4):275-7. doi: 10.1159/000015045. Cytogenet Cell Genet. 1998. PMID: 9730618

2

A novel human gene, encoding a potential membrane protein conserved from yeast to man, is strongly expressed in testis and cancer cell lines.

Veitia RA, Ottolenghi C, Bissery MC, Fellous A. Veitia RA, et al. Among authors: ottolenghi c. Cytogenet Cell Genet. 1999;85(3-4):217-20. doi: 10.1159/000015296. Cytogenet Cell Genet. 1999. PMID: 10449901

3

The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain.

Ottolenghi C, Veitia R, Quintana-Murci L, Torchard D, Scapoli L, Souleyreau-Therville N, Beckmann J, Fellous M, McElreavey K. Ottolenghi C, et al. Genomics. 2000 Mar 1;64(2):170-8. doi: 10.1006/geno.2000.6121. Genomics. 2000. PMID: 10729223

4

Novel paralogy relations among human chromosomes support a link between the phylogeny of doublesex-related genes and the evolution of sex determination.

Ottolenghi C, Fellous M, Barbieri M, McElreavey K. Ottolenghi C, et al. Genomics. 2002 Mar;79(3):333-43. doi: 10.1006/geno.2002.6711. Genomics. 2002. PMID: 11863363

5

The human doublesex-related gene, DMRT2, is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript.

Ottolenghi C, Veitia R, Barbieri M, Fellous M, McElreavey K. Ottolenghi C, et al. Genomics. 2000 Mar 1;64(2):179-86. doi: 10.1006/geno.2000.6120. Genomics. 2000. PMID: 10729224

6

Deletions of 9p and the quest for a conserved mechanism of sex determination.

Ottolenghi C, McElreavey K. Ottolenghi C, et al. Mol Genet Metab. 2000 Sep-Oct;71(1-2):397-404. doi: 10.1006/mgme.2000.3060. Mol Genet Metab. 2000. PMID: 11001833 Review.

7

Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.

Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K. Ottolenghi C, et al. J Clin Endocrinol Metab. 2001 Jun;86(6):2465-9. doi: 10.1210/jcem.86.6.7539. J Clin Endocrinol Metab. 2001. PMID: 11397841

8

Testis determination in mammals: more questions than answers.

Veitia RA, Salas-Cortés L, Ottolenghi C, Pailhoux E, Cotinot C, Fellous M. Veitia RA, et al. Among authors: ottolenghi c. Mol Cell Endocrinol. 2001 Jun 20;179(1-2):3-16. doi: 10.1016/s0303-7207(01)00460-9. Mol Cell Endocrinol. 2001. PMID: 11420125 Review.

9

Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses.

Vialard F, Ottolenghi C, Gonzales M, Choiset A, Girard S, Siffroi JP, McElreavey K, Vibert-Guigue C, Sebaoun M, Joyé N, Portnoï MF, Jaubert F, Fellous M. Vialard F, et al. Among authors: ottolenghi c. J Med Genet. 2002 Jul;39(7):514-8. doi: 10.1136/jmg.39.7.514. J Med Genet. 2002. PMID: 12114486 Free PMC article. No abstract available.

10

The genomic structure of c14orf1 is conserved across eukarya.

Ottolenghi C, Daizadeh I, Ju A, Kossida S, Renault G, Jacquet M, Fellous A, Gilbert W, Veitia R. Ottolenghi C, et al. Mamm Genome. 2000 Sep;11(9):786-8. doi: 10.1007/s003350010148. Mamm Genome. 2000. PMID: 10967139

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

207 results

Search Page

Filters