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21 in total

Review 1. The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations.

Authors: Cecilia Martin; Ravikumar Balasubramanian; Andrew A Dwyer; Margaret G Au; Yisrael Sidis; Ursula B Kaiser; Stephanie B Seminara; Nelly Pitteloud; Qun-Yong Zhou; William F Crowley
Journal: Endocr Rev Date: 2010-10-29 Impact factor: 19.871

2. A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).

Authors: V Ventruto; A Cali; L Farina; B Festa; I Ricciardi; L Sebastio
Journal: J Med Genet Date: 1976-02 Impact factor: 6.318

Review 3. Isolated GnRH deficiency: a disease model serving as a unique prism into the systems biology of the GnRH neuronal network.

Authors: Ravikumar Balasubramanian; William F Crowley
Journal: Mol Cell Endocrinol Date: 2011-07-12 Impact factor: 4.102

4. Functional rescue of Kallmann syndrome-associated prokineticin receptor 2 (PKR2) mutants deficient in trafficking.

Authors: Dan-Na Chen; Yan-Tao Ma; Huadie Liu; Qun-Yong Zhou; Jia-Da Li
Journal: J Biol Chem Date: 2014-04-21 Impact factor: 5.157

5. Isolated pituitary gonadotrophin deficiency: gonadotrophin secretion after synthetic luteinizing hormone and follicle stimulation hormone-releasing hormone.

Authors: J C Marshall; P Harsoulis; D C Anderson; A S McNeilly; G M Besser; R Hall
Journal: Br Med J Date: 1972-12-16

Effect of purified luteinizing hormone releasing factor on normal and hypogonadotrophic anosmic men.

Review 1. The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations.

2. A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).

Review 3. Isolated GnRH deficiency: a disease model serving as a unique prism into the systems biology of the GnRH neuronal network.

4. Functional rescue of Kallmann syndrome-associated prokineticin receptor 2 (PKR2) mutants deficient in trafficking.

5. Isolated pituitary gonadotrophin deficiency: gonadotrophin secretion after synthetic luteinizing hormone and follicle stimulation hormone-releasing hormone.

6. Biochemical and MRI findings of Kallmann's syndrome.

7. Molecular basis for the Kallmann syndrome-linked fibroblast growth factor receptor mutation.

8. Kallmann syndrome.

9. Expression of the KAL gene in multiple neuronal sites during chicken development.

10. Early expression of the KAL gene during embryonic development of the chick.