Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Dysgénésie gonade")

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 96

  • Page / 4
Export

Selection :

  • and

Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systemsDIPIETROMARIA, Aurélie; BENAYOUN, Bérénice A; TODESCHINI, Anne-Laure et al.Human molecular genetics (Print). 2009, Vol 18, Num 17, pp 3324-3333, issn 0964-6906, 10 p.Article

Looks can be deceiving. CommentaryMATTHEWS, Kellie S.Obstetrics and gynecology (New York. 1953). 2007, Vol 109, Num 6, issn 0029-7844, 1449, 1462 [2 p.]Article

ABNORMAL SEX DETERMINATION AND DIFFERENTIATION IN MANBOCZKOWSKI K.1973; OBSTETR. AND GYNECOL.; U.S.A.; DA. 1973; VOL. 41; NO 2; PP. 310-314; BIBL. 28REF.Article

Swyer syndrome : presentation and outcomesMICHALA, L; GOSWAMI, D; CREIGHTON, S. M et al.BJOG (Oxford. Print). 2008, Vol 115, Num 6, pp 737-741, issn 1470-0328, 5 p.Article

MESURE DE LA CAPACITE DE LIAISON DE LA TRANSCORTINE DANS LE SYNDROME DE PSEUDOHERMAPHRODISME MALE AVEC FEMINISATION TESTICULAIRETREMBLAY RR; HO KIM MA; MIGEON CJ et al.1975; UN. MED. CANADA; CANADA; DA. 1975; VOL. 104; NO 3; PP. 411-413; ABS. ANGL.; BIBL. 10REF.Serial Issue

PITUITARY HORMONE SECRETION IN THE GENETICALLY MALE RAT PSEUDOHERMAPHRODITE = SECRETION D'HORMONE HYPOPHYSAIRE CHEZ LE RAT PSEUDOHERMAPHRODITE GENETIQUEMENT MALEGOLDMAN AS; ROOT AW; DUCKETT G et al.1975; J. ENDOCRINOL.; G.B.; DA. 1975; VOL. 64; NO 2; PP. 249-255; BIBL. 1 P.Article

Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivationBEYSEN, Diane; MOUMNE, Lara; VEITIA, Reiner et al.Human molecular genetics (Print). 2008, Vol 17, Num 13, pp 2030-2038, issn 0964-6906, 9 p.Article

Indications for familial screening and gonadectomy in patients with 46,XY gonadal dysgenesisDIMITRI, P; COHEN, M; WRIGHT, N et al.International journal of gynaecology and obstetrics. 2006, Vol 95, Num 2, pp 167-168, issn 0020-7292, 2 p.Article

A de novo phe67leu mutation in the SRY gene in a patient with complete 46,XY gonadal dysgenesisZENTENO, J. C; CARRANZA-LIRA, S; JIMENEZ, A. L et al.Journal of endocrinological investigation (Testo stampato). 2003, Vol 26, Num 11, pp 1117-1119, issn 0391-4097, 3 p.Article

A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretationDALGAARD, Marlene D; WEINHOLD, Nils; GIWERCMAN, Yvonne L et al.Journal of medical genetics. 2012, Vol 49, Num 1, pp 58-65, issn 0022-2593, 8 p.Article

Sexual Quality of Life of Individuals With Disorders of Sex Development and a 46,XY Karyotype: A Review of International ResearchSCHÖNBUCHER, Verena; SCHWEIZER, Katinka; RICHTER-APPELT, Hertha et al.Journal of sex and marital therapy. 2010, Vol 36, Num 3, pp 193-215, issn 0092-623X, 23 p.Article

High incidence of Y-chromosome microdeletions in gonadal tissues from patients with 45,X/46,XY gonadal dysgenesisALVAREZ-NAVA, Francisco; PUERTA, Herminia; SOTO, Marisol et al.Fertility and sterility. 2008, Vol 89, Num 2, pp 458-460, issn 0015-0282, 3 p.Article

Talla baja en varones con fenotipo normal y mosaicismo 45,X/46,XY = LOW STATURE IN MALES WITH NORMAL PHENOTYPE AND 45,X/46,XY MOSAICISMLARA OREJAS, E; GOLMAYO GAZTELU, L; NUNEZ ESTEVEZ, M et al.Anales de pediatria (2003. Ed. impresa). 2008, Vol 68, Num 2, pp 140-142, issn 1695-4033, 3 p.Article

A novel polyalanine expansion in FOXL2 : the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunctionNALLATHAMBI, Jeyabalan; MOUMNE, Lara; DE BAERE, Elfride et al.Human genetics. 2007, Vol 121, Num 1, pp 107-112, issn 0340-6717, 6 p.Article

Mutations in the Desert hedgehog (DHH) gene in patients with 46,XY complete pure gonadal dysgenesisCANTO, P; SÖDERLUND, D; REYES, E et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 9, pp 4480-4483, issn 0021-972X, 4 p.Article

Choix de sexe dans les dysgénésies gonadiques partielles XY (cas clinique) = Sex of rearing in 46,XY partial gonadal dysgenesis (case report)IRAQI, N; GAOUZI, A; BOUHAFS, M. A et al.Annales d'endocrinologie. 2010, Vol 71, Num 2, pp 117-120, issn 0003-4266, 4 p.Article

Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress : evidence for a regulatory imbalance induced by disease-causing mutationsBENAYOUN, Bérénice A; BATISTA, Frank; AUER, Jana et al.Human molecular genetics (Print). 2009, Vol 18, Num 4, pp 632-644, issn 0964-6906, 13 p.Article

Testicular dysgenesis syndrome: foetal origin of adult reproductive problemsWOHLFAHRT-VEJE, Christine; MAIN, Katharina M; SKAKKEBAEK, Niels Erik et al.Clinical endocrinology (Oxford. Print). 2009, Vol 71, Num 4, pp 459-465, issn 0300-0664, 7 p.Article

Génétique : Génétique et anomalies de la détermination sexuelle : Génétique et ReproductionMAITROT, Lorraine; RAVEL, Célia.Reproduction humaine et hormones. 2009, Vol 22, Num 1, pp 54-63, issn 0994-3919, 10 p.Article

Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological rolesL'HOTE, David; GEORGES, Adrien; TODESCHIN, Anne Laure et al.Human molecular genetics (Print). 2012, Vol 21, Num 14, pp 3264-3274, issn 0964-6906, 11 p.Article

Ascending aortic aneurysm in a patient with mixed gonadal dysgenesisBAKOTO, N; CORMAN, V; LEGROS, J. J et al.Annales d'endocrinologie. 2011, Vol 72, Num 1, pp 45-47, issn 0003-4266, 3 p.Article

Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian developmentMOUMNE, Lara; DIPIETROMARIA, Aurélie; BATISTA, Frank et al.Human molecular genetics (Print). 2008, Vol 17, Num 7, pp 1010-1019, issn 0964-6906, 10 p.Article

The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant allelesBENAYOUN, Bérénice A; CABURET, Sandrine; DIPIETROMARIA, Aurélie et al.Human molecular genetics (Print). 2008, Vol 17, Num 20, pp 3118-3127, issn 0964-6906, 10 p.Article

Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregationMOUMNE, Lara; FELLOUS, Marc; VEITIA, Reiner A et al.Human molecular genetics (Print). 2005, Vol 14, Num 23, pp 3557-3564, issn 0964-6906, 8 p.Article

Laparoscopic gonadectomy in paediatric and adolescent girls with intersex disordersESEGBONA, Gloria; CUTNER, Alfred; CUCKOW, Peter et al.BJOG (Oxford. Print). 2003, Vol 110, Num 2, pp 210-212, issn 1470-0328, 3 p.Article

  • Page / 4