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Kallmann Syndrome

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Recent Publications on Kallmann Syndrome:

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Testicular expressed genes are missing in familial X-Linked Kallmann syndrome due to two large different deletions in daughter's X chromosomes.
BACKGROUND: X-linked Kallmann syndrome (KS) is caused mainly by point...
17th July, 2008
Pediatric Endocrinology & Metabolic Unit, Soroka Medical University Horm Res. 2008;69(5):276-83. Epub 2008 Feb 6.
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Genetic control of pubertal timing.
PURPOSE OF REVIEW: Puberty is an important developmental and life stage...
16th July, 2008
Division of Pediatric Endocrinology, Rainbow Babies and Children's Curr Opin Pediatr. 2008 Aug;20(4):458-64.
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Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.
Idiopathic hypogonadotropic hypogonadism (IHH) with anosmia (Kallmann...
4th July, 2008
Harvard Center for Reproductive Endocrine Sciences and Reproductive J Clin Invest. 2008 Jul 1;.
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New genes controlling human reproduction and how you find them.
The neuroendocrine control of reproduction in all mammals is governed by a...
4th July, 2008
Boston, Massachusetts. Trans Am Clin Climatol Assoc. 2008;119:29-38.
Homozygous mutation in the prokineticin-receptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: Case Report.
Prokineticin 2 (Prok2) or prokineticin-receptor2 (Prok-R2) gene mutations...
4th July, 2008
Department of Clinical and Experimental Medicine and Surgery, Hum Reprod. 2008 Jul 1;.
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BioNews Results for Kallmann Syndrome:

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Researcher helping to pioneer medical therapy for Fragile X Syndrome presents latest findings
Firstscience.com:  Jul 19 2008 5:09AM Matching: syndrome
J&J found not liable in Motrin lawsuit
CNBC:  Jul 19 2008 4:49AM Matching: syndrome
Drug Company Found Not Liable in Girl's 'Motrin' Blindness
FOXNews.com:  Jul 19 2008 2:35AM Matching: syndrome
J&J found not liable in Motrin lawsuit
IT Business Net:  Jul 19 2008 2:11AM Matching: syndrome
CORRECTED: J&J found not liable in Motrin lawsuit
Yahoo! Canada:  Jul 19 2008 1:28AM Matching: syndrome
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Kallmann Syndrome Clinical Trials:

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A Study to Characterize Epidemiology, Clinical and Genetic Features of Kallmann Syndrome in Finland
Kallmann Syndrome

Kallmann Syndrome Patents:

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US Patent No.Title
5556786 Anhidrotic ectodermal dysplasia gene and method of detecting same
6235713 Vascular endothelial growth factor-D (VEGF-D) polypeptides
6251601 Simultaneous measurement of gene expression and genomic abnormalities using nucleic acid microarrays
6335170 Gene expression in bladder tumors
6465627 DAX-1 protein, methods for production and use thereof

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BioPortfolio Ltd. offers e-mail and postal lists for Kallmann Syndrome scientists - we have details of around 41 individuals working on Kallmann Syndrome .


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Wikipedia excerpt, where present, licenced under the GNU Free Documentation License. Resources from the NCBI applied. Selected MeSH subject headings created and maintained by the US NLM are used in conjunction with additional keywords. 2006-2008 MeSH.
 

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