lscancerdiag.com Report : Visit Site


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    Server:Apache/2...

    The main IP address: 84.34.147.33,Your server Finland,Helsinki ISP:Zoner Oy  TLD:com CountryCode:FI

    The description :toggle navigation home company team diagmmr research contact submit samples diagmmr® - diagnostics innovation our mission is to save lives through early detection of lynch syndrome with easy and accur...

    This report updates in 15-Jun-2018

Created Date:2013-06-23
Changed Date:2017-05-31

Technical data of the lscancerdiag.com


Geo IP provides you such as latitude, longitude and ISP (Internet Service Provider) etc. informations. Our GeoIP service found where is host lscancerdiag.com. Currently, hosted in Finland and its service provider is Zoner Oy .

Latitude: 60.169521331787
Longitude: 24.93544960022
Country: Finland (FI)
City: Helsinki
Region: Uusimaa
ISP: Zoner Oy

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HTTP Header Analysis


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Content-Encoding:gzip
Transfer-Encoding:chunked
Set-Cookie:3a2bf91d503c8bc61399473693888a1e=6hso5r673mlnt3v8hbkg5mg8d3; path=/; HttpOnly
Vary:User-Agent
Keep-Alive:timeout=2, max=100
Server:Apache/2
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ETag:http://www.lscancerdiag.com/
Pragma:no-cache
Cache-Control:no-cache
Date:Fri, 15 Jun 2018 12:59:39 GMT
Content-Type:text/html; charset=UTF-8

DNS

soa:ns1.zoner.fi. hostmaster.lscancerdiag.com. 2014020400 14400 3600 1209600 86400
ns:ns1.zoner.fi.
ns2.zoner.fi.
ipv4:IP:84.34.147.33
ASN:20569
OWNER:AINAIP-AS http:
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mx:MX preference = 10, mail exchanger = mailscanner02.zoner.fi.
MX preference = 10, mail exchanger = mailscanner01.zoner.fi.

HtmlToText

toggle navigation home company team diagmmr research contact submit samples diagmmr® - diagnostics innovation our mission is to save lives through early detection of lynch syndrome with easy and accurate diagnostic method. lynch syndrome one of the main single causes of colorectal and endometrial cancers, lynch syndrome, i.e. inherited mismatch repair (mmr) deficiency , is carried by up to 1/279 of the population * . inherited defect lynch syndrome (ls) is inherited with 50% probability within affected families. each year, there are 3.5 million new cancer cases within ls spectrum. individual risk individuals with inherited mmr deficiency have more than 70% risk of developing colorectal cancer , compared to 2% in the general population on a global scale. innovative solution the diagmmr ® method developed by ltd is a non-invasive test to detect ls carriers, enabling preventive care and helping save lives. company ltd is committed to reducing cancer mortality rates with a low-cost, simple diagnostic method that detects an inherited cancer-causing condition prior to cancer. our vision is to see diagmmr ® as a new global testing standard in ls diagnostics. lynch syndrome is the main cause of hereditary colorectal cancers and it also causes a broad spectrum of other tumors. with a significant proportion of the world’s population carrying the lynch syndrome mutation, there are potentially tens of millions under a severe risk for being affected by ls. our groundbreaking diagmmr ® assay is an easy functional test that can be used for diagnosis of mmr deficiency i.e. lynch syndrome (previously known as hereditary non­polyposis colorectal cancer; hnpcc). our mission is to save lives through an innovation that dramatically simplifies diagnostics of lynch syndrome by delivering predictive and accurate results with a fast, unique and cost-efficient method globally. team professor minna nyström (prev. nyström­-lahti), phd founder and chairman professor nyström is the leading inventor of diagmmr ® with more than 20 years of experience in the field of lynch syndrome research and has had an active role in both the identification of the ls related genes and mutations as well as the bettering of ls recognition through over 50 scientific publications in the field. prof. nyström is an active member of the international society for gastrointestinal hereditary tumours, insight. dr. minttu kansikas, phd r&d director dr. kansikas has worked on lynch syndrome research in prof. nyström ́s lab for over 9 years and is a co-inventor of diagmmr ® . her doctoral thesis, “recognizing lynch syndrome by dna mismatch repair deficiency” focused on pathogenicity assessment and interpretation of ls associated mutations and functional detection of reduced mismatch repair. mariann kasela, msc researcher msc kasela works as a researcher in ltd and specializes in the functional assessment of mmr proteins. she has broad experience in mmr research, cell culture and biotechnology. dr. jaana putula, phd researcher dr. putula has vast experience in cell culture and works to ensure the meticulous handling of patient samples from sampling to testing. in addition to coordinating the sample handling and running the cell culture processes, she assists with other processes of the diagmmr ® testing. niklas lahti cfo mr. lahti is responsible for managing the strategy and financials of the company and leads the commercialization of the diagmmr ® . he has experience from investment banking and other industries before joining ltd. dr. jukka kantelinen, phd laboratory director dr. kantelinen has worked on dna mismatch repair research in prof. nyström ́s lab for over 11 years. his doctoral thesis, “functional characterization of muts homologue mismatch repair proteins and their variants” focused on functional characterization of ls mutations and the key molecular components of the mmr mechanism. dr. laura vähätalo, phd production manager dr. vähätalo is responsible for the laboratory production of the diagmmr ® assay, as well as the interpretation and management of the results. in addition to the production management, she also specializes in the quantitative detection method. she has extensive experience in molecular biology techniques and biomedical research. anni moilanen, msc researcher msc moilanen works as a researcher in the team. her role is central in producing the molecular components used in diagmmr ® . she has broad experience in molecular biology techniques and also contributes to the cell culture processes and other functions of the lab. from sample to diagnosis diagmmr ® is designed to be a predictive diagnostic tool that enables preventive follow-up and counselling for affected mutation carriers who are at high risk for developing lynch syndrome related cancers. while current ls diagnosis relies on tumor studies, the quantitative diagmmr ® method allows carrier diagnosis based on a non-invasive tissue sample before the person has developed a cancer, without the knowledge and details of an inherited mutation. diagnostic benefits the diagmmr ® innovation has several outstanding benefits compared to the current diagnostic tools: diagmmr ® diagnoses lynch syndrome from a non-malignant tissue sample before tumors appear making it predictive instead of reactive. diagmmr ® is a fast single functional test replacing the current large array of tests. diagmmr ® delivers results that are easy to interpret. diagmmr ® costs less than current test panels, saving significantly in healthcare costs on a global scale. international lynch syndrome research inherited mmr deficiency, i.e. lynch syndrome, gives rise to a broad spectrum of tumors, especially colorectal and endometrial cancers, but also ovarian, gastric, urinary, small bowel, brain and bile duct/gallbladder cancers. the history of international lynch syndrome research can be traced back to 1895 and the discovery of a family cancer syndrome . the disease was characterized by henry t. lynch in 1966 and came to be known as hereditary nonpolyposis colorectal cancer (hnpcc), which in honour of dr. lynch’s findings, was later termed lynch syndrome. the molecular genetics era began in 1993 when a germline mmr gene mutation was identified as a cause of ls . currently lynch syndrome research is being actively carried out worldwide, with an approach that focuses on obtaining a deeper understanding of the molecular mechanism behind ls, enabling preventive diagnosis and personalized medical care. resources international society for gastrointestinal hereditary tumors (insight) is an international multidisciplinary, scientific organization with the mission to improve the quality of care of patients and their families with any condition resulting in hereditary gastrointestinal tumors. the inventors, scientific advisors, key collaborators, and ltd employees have actively participated in the activities of insight. finnish hnpcc is a group formed by leading finnish lynch syndrome researchers. the group is actively involved in several projects on the mmr mechanism and ls in collaboration with central university hospitals in finland. international agency for cancer research (iarc) is the specialized cancer agency of the world health organization. the objective of the iarc is to promote international collaboration in cancer research to adopt preventive measures and reduce cancer mortality. academic research root of diagmmr® the diagmmr ® innovation is based on more than 20 years of academic research at the university of helsinki, where the functional mmr assay research and development has resulted in 7 phds and 30 original peer-reviewed publications in the 2000's. diagmmr ® is an advanced application of an in vitro mmr assay used for the functional characterization of mmr gene mutations. publications nyström, m. & kansikas, m. (2017) predictive cancer diagnostics: ltd has developed diagmmr, an innovative method to detect cancer syndrome before cancers form. pan e

URL analysis for lscancerdiag.com


http://www.lscancerdiag.com//#contact
http://www.lscancerdiag.com/#team
http://www.lscancerdiag.com/
http://www.lscancerdiag.com/#diagmmr
http://www.lscancerdiag.com/#home
http://www.lscancerdiag.com/#research
http://www.lscancerdiag.com/#company
edition.pagesuite-professional.co.uk

Whois Information


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Domain Name: LSCANCERDIAG.COM
Registry Domain ID: 1810324505_DOMAIN_COM-VRSN
Registrar WHOIS Server: whois.joker.com
Registrar URL: http://www.joker.com
Updated Date: 2017-05-31T10:27:27Z
Creation Date: 2013-06-23T12:42:09Z
Registry Expiry Date: 2018-06-23T12:42:09Z
Registrar: CSL Computer Service Langenbach GmbH d/b/a joker.com
Registrar IANA ID: 113
Registrar Abuse Contact Email: [email protected]
Registrar Abuse Contact Phone: +49.21186767447
Domain Status: clientTransferProhibited https://icann.org/epp#clientTransferProhibited
Name Server: NS1.VERKKOTAIKURIT.FI
Name Server: NS2.VERKKOTAIKURIT.FI
DNSSEC: unsigned
URL of the ICANN Whois Inaccuracy Complaint Form: https://www.icann.org/wicf/
>>> Last update of whois database: 2017-10-14T11:52:49Z <<<

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  REGISTRAR CSL Computer Service Langenbach GmbH d/b/a joker.com

SERVERS

  SERVER com.whois-servers.net

  ARGS domain =lscancerdiag.com

  PORT 43

  TYPE domain

DOMAIN

  NAME lscancerdiag.com

  CHANGED 2017-05-31

  CREATED 2013-06-23

STATUS
clientTransferProhibited https://icann.org/epp#clientTransferProhibited

NSERVER

  NS1.VERKKOTAIKURIT.FI 84.34.166.22

  NS2.VERKKOTAIKURIT.FI 84.34.147.22

  REGISTERED yes

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