Ushbu ish iqtibos qilgan ishlar

25 ta ish

Ish: "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
Sharh maqola20093 iqtibos
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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
Maqola19972 iqtibos
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Isolation and properties of the FSH and LH-releasing hormone
Andrew V. Schally, Akira Arimura, Yukihiro Baba +5
Maqola19712 iqtibos
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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
Maqola19412 iqtibos
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Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2
Catherine Dodé, Luís Teixeira, Jacqueline Levilliers +15
Maqola20062 iqtibos
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Gonadotropin‐releasing hormone‐1 (GnRH‐1) is involved in tooth maturation and biomineralization
Jean D. R. Tiong, Thomas Locastro, Susan Wray
Maqola20072 iqtibos
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THE RELATION OF THE NERVOUS SYSTEM TO OVULATION AND OTHER PHENOMENA OF THE FEMALE REPRODUCTIVE TRACT
J. C. Hinsey
Maqola19372 iqtibos
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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
Maqola20082 iqtibos
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A Family with Hypogonadotropic Hypogonadism and Mutations in the Gonadotropin-Releasing Hormone Receptor
Nicolás de Roux, Jacques Young, Micheline Misrahi +4
Maqola19972 iqtibos
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The induction of ovulation in the rabbit, by electrical stimulation of the hypothalamo-hypophysial mechanism
G. W. Harris
Maqola19372 iqtibos
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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
Maqola19712 iqtibos
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The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
Renaud Legouis, Jean‐Pierre Hardelin, Jacqueline Levilliers +7
Maqola19912 iqtibos
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Clinical Manifestations of Impaired GnRH Neuron Development and Function
Hyung‐Goo Kim, Balasubramanian Bhagavath, Lawrence C. Layman
Sharh maqola20082 iqtibos
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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont +27
Maqola20032 iqtibos
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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
Maqola19912 iqtibos
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Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
Hyung‐Goo Kim, Ingo Kurth, Fei Lan +13
Maqola20082 iqtibos
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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
Maqola20082 iqtibos
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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
Maqola20032 iqtibos
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A STUDY OF THE MECHANISM WHEREBY COITUS EXCITES THE OVULATION-PRODUCING ACTIVITY OF THE RABBIT'S PITUITARY
Chandler McCuskey Brooks
Maqola19372 iqtibos
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Sarlavhasiz
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