Ушбу иш иқтибос қилган ишлар

25 та иш

Иш: "The significance of the GNRH 1 gene polymorphism (rs 6185, rs1812594) in the development of idiopathic hypogonadotropic hypogonadism."

What controls the timing of puberty? An update on progress from genetic investigation
Zofia K. Z. Gajdos, Joel N. Hirschhorn, Mark R. Palmert
Шарҳ мақола20093 иқтибос
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Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene
Robert S. Jackson, John W.M. Creemers, Shinya Ohagi +5
Мақола19972 иқтибос
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Isolation and properties of the FSH and LH-releasing hormone
Andrew V. Schally, Akira Arimura, Yukihiro Baba +5
Мақола19712 иқтибос
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RELEASE OF LUTEINIZING HORMONE FROM THE ANTERIOR HYPOPHYSIS BY AN ACETYLCHOLINE-LIKE SUBSTANCE FROM THE HYPOTHALAMIC REGION
M. Taubenhaus, Samuel Soskin
Мақола19412 иқтибос
ABI
Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2
Catherine Dodé, Luís Teixeira, Jacqueline Levilliers +15
Мақола20062 иқтибос
ABI
Gonadotropin‐releasing hormone‐1 (GnRH‐1) is involved in tooth maturation and biomineralization
Jean D. R. Tiong, Thomas Locastro, Susan Wray
Мақола20072 иқтибос
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THE RELATION OF THE NERVOUS SYSTEM TO OVULATION AND OTHER PHENOMENA OF THE FEMALE REPRODUCTIVE TRACT
J. C. Hinsey
Мақола19372 иқтибос
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TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction
A. Kemal Topaloğlu, Frank Reimann, Metin Güçlü +12
Мақола20082 иқтибос
ABI
A Family with Hypogonadotropic Hypogonadism and Mutations in the Gonadotropin-Releasing Hormone Receptor
Nicolás de Roux, Jacques Young, Micheline Misrahi +4
Мақола19972 иқтибос
ABI
The induction of ovulation in the rabbit, by electrical stimulation of the hypothalamo-hypophysial mechanism
G. W. Harris
Мақола19372 иқтибос
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Purification, amino acid composition and N-terminus of the hypothalamic luteinizing hormone releasing factor (LRF) of ovine origin
Max S. Amoss, Roger Burgus, Richard E. Blackwell +3
Мақола19712 иқтибос
ABI
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
Renaud Legouis, Jean‐Pierre Hardelin, Jacqueline Levilliers +7
Мақола19912 иқтибос
ABI
Clinical Manifestations of Impaired GnRH Neuron Development and Function
Hyung‐Goo Kim, Balasubramanian Bhagavath, Lawrence C. Layman
Шарҳ мақола20082 иқтибос
ABI
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont +27
Мақола20032 иқтибос
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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
Brunella Franco, Silvana Guioli, Antonella Pragliola +13
Мақола19912 иқтибос
ABI
Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
Hyung‐Goo Kim, Ingo Kurth, Fei Lan +13
Мақола20082 иқтибос
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Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice
John Falardeau, W. C. Chung, Andrew Beenken +18
Мақола20082 иқтибос
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Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
Nicolás de Roux, Emmanuelle Génin, Jean‐Claude Carel +3
Мақола20032 иқтибос
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A STUDY OF THE MECHANISM WHEREBY COITUS EXCITES THE OVULATION-PRODUCING ACTIVITY OF THE RABBIT'S PITUITARY
Chandler McCuskey Brooks
Мақола19372 иқтибос
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Сарлавҳасиз
Бошқа2 иқтибос
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Сарлавҳасиз
Бошқа1 иқтибос
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Сарлавҳасиз
Бошқа1 иқтибос
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Сарлавҳасиз
Бошқа1 иқтибос
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Сарлавҳасиз
Бошқа1 иқтибос
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Сарлавҳасиз
Бошқа1 иқтибос
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