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A novel mutation in the anti-müllerian hormone gene as cause of persistent müllerian duct syndrome.
- Published in:
- 2001
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- Publication type:
- journal article
GnRH Transactivates Human AMH Receptor Gene via Egr1 and FOXO1 in Gonadotrope Cells.
- Published in:
- Neuroendocrinology, 2019, v. 108, n. 2, p. 65, doi. 10.1159/000494890
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- Publication type:
- Article
The Bone Morphogenetic Protein 15 Up-Regulates the Anti-Müllerian Hormone Receptor Expression in Granulosa Cells.
- Published in:
- 2016
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- Publication type:
- journal article
Subcellular and Molecular Mechanisms Regulating Anti-Müllerian Hormone Gene Expression in Mammalian and Nonmammalian Species.
- Published in:
- DNA & Cell Biology, 2004, v. 23, n. 9, p. 572, doi. 10.1089/1044549041939232
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- Publication type:
- Article
Different patterns of anti-Müllerian hormone expression, as related to DMRT1, SF-1, WT1, GATA-4, Wnt-4, and Lhx9 expression, in the chick differentiating gonads.
- Published in:
- Developmental Dynamics, 2002, v. 225, n. 3, p. 221, doi. 10.1002/dvdy.10153
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- Publication type:
- Article
Early expression of AMH in chicken embryonic gonads precedes testicular SOX9 expression.
- Published in:
- Developmental Dynamics, 1998, v. 212, n. 4, p. 522, doi. 10.1002/(SICI)1097-0177(199808)212:4<522::AID-AJA5>3.0.CO;2-J
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- Publication type:
- Article
Nathalie Josso, MD, PhD, 1934–2022.
- Published in:
- Hormone Research in Paediatrics, 2024, v. 97, n. 2, p. 211, doi. 10.1159/000531768
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- Publication type:
- Article
Anti-Müllerian Hormone Recruits BMPR-IA in Immature Granulosa Cells.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081551
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- Publication type:
- Article
Genome-Wide High-Resolution aCGH Analysis of Gestational Choriocarcinomas.
- Published in:
- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029426
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- Publication type:
- Article
Lack of androgen receptor expression in Sertoli cells accounts for the absence of anti-Mullerian hormone repression during early human testis development.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Autosomal Recessive Segregation of a Truncating Mutation of Anti-Müllerian Type II Receptor in a Family Affected by the Persistent Müllerian Duct Syndrome Contrasts with Its Dominant Negative Activity in Vitro.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 9, p. 4390, doi. 10.1210/jcem.86.9.7839
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- Publication type:
- Article
Clinical aspects and molecular genetics of the persistent Müllerian duct syndrome.
- Published in:
- Clinical Endocrinology, 1997, v. 47, n. 2, p. 137, doi. 10.1046/j.1365-2265.1997.2411044.x
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- Publication type:
- Article
Role of type I receptors for anti-Müllerian hormone in the SMAT-1 Sertoli cell line.
- Published in:
- Oncogene, 2005, v. 24, n. 31, p. 4984, doi. 10.1038/sj.onc.1208686
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- Publication type:
- Article
Persistent Müllerian Duct Syndrome: A Rare But Important Etiology of Inguinal Hernia and Cryptorchidism.
- Published in:
- Sexual Development, 2019, v. 13, n. 5/6, p. 264, doi. 10.1159/000510466
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- Publication type:
- Article
The Persistent Müllerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases.
- Published in:
- Sexual Development, 2017, v. 11, n. 3, p. 109, doi. 10.1159/000475516
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- Publication type:
- Article
A novel mutation in the AMHR2 gene, resulting in persistent Müllerian duct syndrome presenting with bilateral cryptorchidism and obstructed inguinal hernia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2023, v. 36, n. 9, p. 890, doi. 10.1515/jpem-2023-0245
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- Publication type:
- Article
Persistent Müllerian duct syndrome associated with genetic defects in the regulatory subunit of myosin phosphatase.
- Published in:
- 2022
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- Publication type:
- journal article
Loss of LH-induced down-regulation of anti-Mullerian hormone receptor expression may contribute to anovulation in women with polycystic ovary syndrome.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Loss of LH-induced down-regulation of anti-Müllerian hormone receptor expression may contribute to anovulation in women with polycystic ovary syndrome.
- Published in:
- Human Reproduction, 2013, v. 28, n. 3, p. 762, doi. 10.1093/humrep/des460
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- Publication type:
- Article
Altered p16 and Bcl-2 Expression Reflects Pathologic Development in Hydatidiform Moles and Choriocarcinoma.
- Published in:
- Pathology & Oncology Research, 2013, v. 19, n. 2, p. 217, doi. 10.1007/s12253-012-9572-2
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- Publication type:
- Article
La série québécoise du nouveau millénaire : une sérietélé distinctive.
- Published in:
- Alternative Francophone, 2015, v. 1, n. 8, p. 1
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- Publication type:
- Article
A mutation inactivating the distal SF1 binding site on the human anti-Müllerian hormone promoter causes persistent Müllerian duct syndrome.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 19, p. 3211, doi. 10.1093/hmg/ddz147
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- Publication type:
- Article
Mutations of the AMH Type II Receptor in Two Extended Families with Persistent Müllerian Duct Syndrome: Lack of Phenotype/Genotype Correlation.
- Published in:
- Hormone Research in Paediatrics, 2012, v. 77, n. 5, p. 291, doi. 10.1159/000338343
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- Publication type:
- Article
Differential expression of E-cadherin, β-catenin, and Lewis x between invasive hydatidiform moles and post-molar choriocarcinomas.
- Published in:
- Virchows Archiv: European Journal of Pathology, 2013, v. 462, n. 6, p. 653, doi. 10.1007/s00428-013-1427-z
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- Publication type:
- Article
Differential expression of E-cadherin, β-catenin, and Lewis x between invasive hydatidiform moles and post-molar choriocarcinomas.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Natural mutations of the anti-Müllerian hormone type II receptor found in persistent Müllerian duct syndrome affect ligand binding, signal transduction and cellular transport.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 16, p. 3002, doi. 10.1093/hmg/ddp238
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- Publication type:
- Article
Unexpected mosaicism of R201H-GNAS1 mutant-bearing cells in the testes underlie macro-orchidism without sexual precocity in McCune–Albright syndrome.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3538, doi. 10.1093/hmg/ddl430
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- Publication type:
- Article
Anti-Müllerian Hormone: A Valuable Addition to the Toolbox of the Pediatric Endocrinologist.
- Published in:
- International Journal of Endocrinology, 2013, p. 1, doi. 10.1155/2013/674105
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- Publication type:
- Article
Anti-Müllerian Hormone and Its Clinical Use in Pediatrics with Special Emphasis on Disorders of Sex Development.
- Published in:
- International Journal of Endocrinology, 2013, p. 1, doi. 10.1155/2013/198698
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- Publication type:
- Article
Novel anti-mullerian hormone mutation revealed by haematospermia in a 60-year-old patient.
- Published in:
- Clinical Endocrinology, 2011, v. 74, n. 3, p. 404, doi. 10.1111/j.1365-2265.2010.03903.x
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- Publication type:
- Article
A 27 Base-Pair Deletion of the Anti-Müllerian Type Ii Receptor Gene is the Most Common Cause of the Persistent MüLlerian Duct Syndrome.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 9, p. 1269, doi. 10.1093/hmg/5.9.1269
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- Publication type:
- Article
Molecular genetics of the persistent Müllerian duct syndrome: a study of 19 families.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 1, p. 125
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- Publication type:
- Article