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Results: 1-15 |
Results: 15
Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome
Authors: Chavez, B Mendez, JP Ulloa-Aguirre, A Larrea, F Vilchis, F
Citation: B. Chavez et al., Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome, J HUM GENET, 46(10), 2001, pp. 560-565
A novel homozygous mutation in the second transmembrane domain of the gonadotrophin releasing hormone receptor gene
Authors: Soderlund, D Canto, P de la Chesnaye, E Ulloa-Aguirre, A Mendez, JP
Citation: D. Soderlund et al., A novel homozygous mutation in the second transmembrane domain of the gonadotrophin releasing hormone receptor gene, CLIN ENDOCR, 54(4), 2001, pp. 493-498
Changes in the biological: immunological ratio of basal and GnRH-releasable FSH during the follicular, pre-ovulatory and luteal phases of the human menstrual cycle
Authors: Zarinan, T Olivares, A Soderlund, D Mendez, JP Ulloa-Aguirre, A
Citation: T. Zarinan et al., Changes in the biological: immunological ratio of basal and GnRH-releasable FSH during the follicular, pre-ovulatory and luteal phases of the human menstrual cycle, HUM REPR, 16(8), 2001, pp. 1611-1618
Is there any physiological role for gonadotrophin oligosaccharide heterogeneity in humans? I. Gonadotrophins are synthesized and released in multiplemolecular forms. A matter of fact
Authors: Ulloa-Aguirre, A Timossi, C Mendez, JP
Citation: A. Ulloa-aguirre et al., Is there any physiological role for gonadotrophin oligosaccharide heterogeneity in humans? I. Gonadotrophins are synthesized and released in multiplemolecular forms. A matter of fact, HUM REPR, 16(4), 2001, pp. 599-604
Clinical expression and SRY gene analysis in XY subjects lacking gonadal tissue
Authors: Zenteno, JC Jimenez, AL Canto, P Valdez, H Mendez, JP Kofman-Alfaro, S
Citation: Jc. Zenteno et al., Clinical expression and SRY gene analysis in XY subjects lacking gonadal tissue, AM J MED G, 99(3), 2001, pp. 244-247
No evidence of mutations in the follicle-stimulating hormone receptor genein Mexican women with 46,XX pure gonadal dysgenesis
Authors: de la Chesnaye, E Canto, P Ulloa-Aguirre, A Mendez, JP
Citation: E. De La Chesnaye et al., No evidence of mutations in the follicle-stimulating hormone receptor genein Mexican women with 46,XX pure gonadal dysgenesis, AM J MED G, 98(2), 2001, pp. 125-128
Identification of missense mutations in the SRD5A2 gene from patients withsteroid 5 alpha-reductase 2 deficiency
Authors: Vilchis, F Mendez, JP Canto, P Lieberman, E Chavez, B
Citation: F. Vilchis et al., Identification of missense mutations in the SRD5A2 gene from patients withsteroid 5 alpha-reductase 2 deficiency, CLIN ENDOCR, 52(3), 2000, pp. 383-387
Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA
Authors: Jimenez, AL Kofman-Alfaro, S Berumen, J Hernandez, E Canto, P Mendez, JP Zenteno, JC
Citation: Al. Jimenez et al., Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA, AM J MED G, 93(5), 2000, pp. 417-420
A mutation in the 5 ' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism
Authors: Canto, P de la Chesnaye, E Lopez, M Cervantes, A Chavez, B Vilchis, F Reyes, E Ulloa-Aguirre, A Kofman-Alfaro, S Mendez, JP
Citation: P. Canto et al., A mutation in the 5 ' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism, J CLIN END, 85(5), 2000, pp. 1908-1911
A preponderance of circulating basic isoforms is associated with decreasedplasma half-life and biological to immunological ratio of gonadotropin-releasing hormone-releasable luteinizing hormone obese men
Authors: Castro-Fernandez, C Olivares, A Soderlund, D Lopez-Alvarenga, JC Zambrano, E Veldhuis, JD Ulloa-Aguirre, A Mendez, JP
Citation: C. Castro-fernandez et al., A preponderance of circulating basic isoforms is associated with decreasedplasma half-life and biological to immunological ratio of gonadotropin-releasing hormone-releasable luteinizing hormone obese men, J CLIN END, 85(12), 2000, pp. 4603-4610
Renal abnormalities in patients with Kallmann syndrome
Authors: Zenteno, JC Mendez, JP Maya-Nunez, G Ulloa-Aguirre, A Kofman-Alfaro, S
Citation: Jc. Zenteno et al., Renal abnormalities in patients with Kallmann syndrome, BJU INT, 83(4), 1999, pp. 383-386
Scant XYqh- testicular cells with normal SRY was enough to differentiate bilateral testes in a 45,X/46,XYqh- patient
Authors: Mendez, JP Canto, P Lopez, M de la Chesnaye, E Torres, L Chavez, B Ulloa-Aguirre, A Kofman-Alfaro, S
Citation: Jp. Mendez et al., Scant XYqh- testicular cells with normal SRY was enough to differentiate bilateral testes in a 45,X/46,XYqh- patient, EUR J OB GY, 87(2), 1999, pp. 159-162
An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis
Authors: Maya-Nunez, G Torres, L Ulloa-Aguirre, A Zenteno, JC Cuevas-Covarrubias, S Saavedra-Ontiveros, D Kofman-Alfaro, S Mendez, JP
Citation: G. Maya-nunez et al., An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis, CLIN ENDOCR, 50(2), 1999, pp. 157-162
Ascertainment and mutational studies of SRY in nine XY females
Authors: Graves, PE Davis, D Erickson, RP Lopez, M Kofman-Alfaro, S Mendez, JP Speer, IE
Citation: Pe. Graves et al., Ascertainment and mutational studies of SRY in nine XY females, AM J MED G, 83(2), 1999, pp. 138-139
Evidence for genetic heterogeneity in male pseudohermaphroditism due to leydig cell hypoplasia
Authors: Zenteno, JC Canto, P Kofman-Alfaro, S Mendez, JP
Citation: Jc. Zenteno et al., Evidence for genetic heterogeneity in male pseudohermaphroditism due to leydig cell hypoplasia, J CLIN END, 84(10), 1999, pp. 3803-3806
Risultati: 1-15 |