Rechercher
Results
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WDR11
WDR11 OMIM 606417 Located at chromosome 10q26.12 E ncodes the WD repeat-containing protein 11, a member of the WD repeat-containing protein family. WD repeats are approximately 30- to 40-amino acid domains that are involved in protein-protein interactions. WDR11 comprises 29 exons and the correspond
chuv.ch/en/hhn/hhn-home/research/gene-curation/wdr11
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Training
Training TRAINING AND EDUCATION A key objective of the Training activities is to provide mentoring and career development opportunities for young investigators to develop the next generation of leaders in the field of Reproductive Medicine and the Neurosciences. Current Training Activites include: S
chuv.ch/en/hhn/hhn-home/neuroendocrine-control-of-reproduction/training
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Donate
Donate
chuv.ch/en/hhn/hhn-home/neuroendocrine-control-of-reproduction/donate
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Learn about GnRH deficiency / Kallmann syndrome
Learn about GnRH deficiency / Kallmann syndrome What is GnRH deficiency? A Brief Overview GnRH deficiency can occur in a number of different conditions and are classed collectively as hypogonadotropic hypogonadism (HH). One type of GnRH deficiency that occurs in conjunction with a lack of sense of s
chuv.ch/en/hhn/hhn-home/patients/learn-about-gnrh-deficiency-kallmann-syndrome
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Patient Resources
Patient Resources Other patients know what it is like to live with congenital hypogonadotropic hypogonadism (CHH, and Kallmann syndrome) on a day-to-day basis. It can be helpful to have contact with these patients to receive support and also to provide support. Below you will find several links to p
chuv.ch/en/hhn/hhn-home/patients/patient-resources
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Our Basic Scientists
Our Basic Scientists Meet our Basic Scientists Our COST Action includes international scientists who apply varied approaches to explore GnRH biology. These investigators utliize genetics studies, cell-based systems and animal models to better understand puberty and reproduction. Click on a picture t
chuv.ch/en/hhn/hhn-home/research/our-basic-scientists
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Patient Registry
Patient Registry Purposes of the registry are: To share information about patients in order to facilitate collaboration for funding, research and publications To create systematic phenotyping of GnRH deficient patients Patient Registry Charter To receive a copy of the Charter please contact Andrew D
chuv.ch/en/hhn/hhn-home/research/patient-registry
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Genetic Research Centres
Genetic Research Centres More that 20 genes have been associated with GnRH deficiency, yet these genes only identify genetics causes of GnRH deficiency in about 50% of cases. Several research centres across Europe are working actively to discover new genes associated with GnRH deficiency (including
chuv.ch/en/hhn/hhn-home/research/genetic-research-centres
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Join a research study
Join a research study There are several online sites for finding research studies involving patients with GnRH deficiency (including those with Kallman syndrome): COST participants conducting research studies on GnRH deficiency are listed to the LEFT. You can contact the investigators directly from
chuv.ch/en/hhn/hhn-home/patients/join-a-research-study
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Gene Curation
Gene Curation We are working in the field of human genetics to develop a comprehensive listing of all the known mutations among the genes associated with GnRH deficiency. A number of participants in our COST Action are helping to curate this ever-changing list. Genes Curators CHD7 Catherine Dodé Nel
chuv.ch/en/hhn/hhn-home/research/gene-curation