The ontogeny of mullerian inhibiting substance in the gonads of the chicken†

Hutson, John M.; Ikawa, Hiromichi; Donahoe, Patricia K.

doi:10.1016/s0022-3468(81)80827-5

Cited by 104 publications

(44 citation statements)

References 12 publications

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“…In females, ovarian AMH expression is delayed, starting around birth in granulosa cells of primary follicles (Bézard et al, 1987). AMH has been cloned in chick (Carré-Eusèbe et al, 1996) and is also expressed in embryonic ovaries (Hutson et al, 1981). The function of AMH in the ovaries is unclear, although it may play a role in ovarian follicle maturation (Durlinger et al, 2001;McGee et al, 2001).…”

Section: Introductionmentioning

confidence: 99%

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

Oréal

Mazaud²,

Picard

et al. 2002

Developmental Dynamics

132

106

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In mammals, anti-Mü llerian hormone (AMH) is produced by Sertoli cells from the onset of testicular differentiation and by granulosa cells after birth. In birds, AMH starts to be expressed in indifferent gonads of both sexes at a similar level and is later upregulated in males. We previously demonstrated that, unlike in mammals, the onset of AMH expression occurs in chick embryo in the absence of SOX9. We looked for potential factors that might be involved in regulating AMH expression at different stages of chick gonad differentiation by comparing its expression pattern in embryos and young chicken with that of DMRT1, SF-1, WT1, GATA-4, Wnt-4, and

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Section: Introductionmentioning

confidence: 99%

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

Oréal

Mazaud²,

Picard

et al. 2002

Developmental Dynamics

132

106

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“…Anti-Müllerian activity has also been demonstrated in embryonic and adult chick ovary (Hutson, Ikawa and Donahoe, 1981). Bioactive AMH released by the granulosa cells has been purified from follicular fluid of mature bovine ovaries (Vigier et al, 1984) ; the synthesis of this ovarian AMH was located by radioimmunoassay and cytochemistry in granulosa cells by Vigier et al (1984) and Takahasi et al (1986).…”

mentioning

confidence: 98%

Anti-Müllerian hormone in sheep follicles

Bézard¹,

Vigier²,

Tran³

et al. 1988

Reprod. Nutr. Dévelop.

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“…Additional roles of MIS in male sexual development, however, have not been well characterized. In females, MIS production by the granulosa cells and presence in the follicular fluid of the postnatal ovary (Hutson et al, 1981;Vigier et al, 1984;Takahashi et al, 1986a;Necklaws et al, 1986) point to a role in female reproductive function (e.g. oocyte meiosis inhibition, see Takahashi et al, 1986b).…”

Section: Sexual Development and Mullerian-inhibiting Substance (Mis)mentioning

confidence: 99%

Transgenic strategies in reproductive endocrinology

Kelley

Johnson

Gwatkin

et al. 1993

Molecular Reproduction Devel

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The present discussion surveys some of the recently published studies utilizing transgenic strategies to address questions in reproductive endocrinology. Beginning with a brief introduction of the transgenic method itself, the following areas are covered: 1. Sexual development and Mullerian-inhibiting substance; 2. Hypogonadal mice and hypothalamic GnRH; 3. The GnRH neuron: generation of immortalized rare cell types; 4. Glycoprotein hormones: immortalized cells, development and evolution; 5. Growth hormone and reproduction; and, 6.Gestation and the insulin-like growth factors. In each section, the discussion attempts to be integrative with respect to the significance of the results to physiological, cellular and molecular biology. We believe this approach is appropriate, as transgenic science itself is necessarily an integration of all of these levels of investigation and participation from those working at all levels is needed. 0 1993 Wiley-Ltss, Inc.

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The ontogeny of mullerian inhibiting substance in the gonads of the chicken†

Cited by 104 publications

References 12 publications

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

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

Anti-Müllerian hormone in sheep follicles

Transgenic strategies in reproductive endocrinology

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