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         Fanconi Anemia:     more books (28)
  1. Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging (Monographs in Human Genetics) by D. Schindler, H. Hoehn, 2007-05-10
  2. Fanconi anemia: A handbook for families & their physicians by Lynn Frohnmayer, 2000
  3. Fanconi Anemia - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-28
  4. Fanconi Anemia: Clinical, Cytogenetic and Experimental Aspects
  5. Molecular Mechanisms Of Fanconi Anemia by Shamim I., Ph.D. Ahmad, 2004-11
  6. FANCONI ANEMIA, A HANDBOOK FOR FAMILIES & THEIR PHYSICIANS , SECOND EDITION
  7. Fanconi Anemia: A Handbook for Families and Their Physicians
  8. The interplay of Fanconi anemia proteins in the DNA damage response [An article from: DNA Repair] by X. Wang, A.D. D'Andrea,
  9. Fanconi anemia: An entry from Thomson Gale's <i>Gale Encyclopedia of Cancer, 2nd ed.</i> by Michelle, M.S., J.D. Johnson, 2006
  10. Fanconi Anemia Medical Guide by Qontro Medical Guides, 2008-07-09
  11. Chromosome 9 Gene Introduction: Traf2, Fancg, Tsc1, Fanconi Anemia, Complementation Group C, Ralgds, Steroidogenic Factor 1, Syk, Dnm1, Smarca2
  12. Dedicated to the core: Understanding the Fanconi anemia complex [An article from: DNA Repair] by A.M. Gurtan, A.D. D'Andrea, 2006-09-08
  13. New insights into the Fanconi anemia pathway from an isogenic FancG hamster CHO mutant [An article from: DNA Repair] by R.S. Tebbs, J.M. Hinz, et all 2005-01-02
  14. The Fanconi anemia pathway limits the severity of mutagenesis [An article from: DNA Repair] by J.M. Hinz, P.B. Nham, et all 2006-08-13

61. Cancer Spectrum Useful Links - Fanconi Anemia
Go To Home Useful Links Causes and Prevention Predisposing Conditions and Syndromes fanconi anemia. Useful Links fanconi anemia.
http://jncicancerspectrum.oupjournals.org/cgi/links/jnciplusLink;CAT_127
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Alerting Editorial Board About JNCI Search JNCI Other Journals ... Search Cancer Statistics Subscriptions Advertising About JNCI Cancer Spectrum Contact Us Go To: Home Useful Links Causes and Prevention Predisposing Conditions and Syndromes
Useful Links - Fanconi Anemia
Submit your suggestion for a Useful Link
Categories:
Web Sites:
Fanconi Anemia Mutation Database
An international collaborative database coordinated by Rockefeller University and Guy's Hospital . The site includes public and private databases, reference sequences, and related links. (USA)
Fanconi Anemia Research Fund
A non-profit organization founded in 1989 to promote research to find effective treatments for FA and to provide education and support. The Web site includes a handbook for families and their physicians, and science newsletters. (USA)

62. Fanconi Anemia, Anemia De Fanconi, Anemia Fanconi Picture
Topics to inquire for fanconi anemia, anemia de fanconi, anemia fanconi picture, anemia fanconi fund research. You can find more on fanconi anemia right now.
http://www.healthinquire.com/fanconi-anemia.html
Topics to inquire for fanconi anemia, anemia de fanconi, anemia fanconi picture, anemia fanconi fund research
Anemia de fanconi Anemia fanconi picture Anemia fanconi fund research Anemia aplastic fanconi
Inquire for fanconi anemia research and fanconi anemia portal List:
Fanconi Anemia Health Forums

Ask questions and chat with others on our health and wellness fourms.
Fairview-University Blood and Marrow Transplant (BMT) Services

University of Minnesota physicians perform blood and marrow transplant (BMT) treatments for metabolic disorders and anemias. Find out about referrals to the program.
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You can find more on: fanconi anemia right now.

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Fairview-University Blood and Marrow Transplant (BMT) Services
University of Minnesota physicians perform blood and marrow transplant (BMT) treatments for metabolic disorders and anemias. Find out about referrals to the program.

63. Ask NOAH About: Anemia
of Pediatrics Understanding Your Complete Blood Count National Institutes of Health (PDF File of 9 Pages) What is fanconi anemia and How is it Diagnosed?
http://www.noah-health.org/english/illness/blood/anemia.html
Ask NOAH About: Anemia
What is Anemia? Care and Treatment Information Resources Basic Descriptions
Anemia in Children
...
Organizations

What Is Anemia?
Basic Descriptions
About Anemia - KidsHealth
All About Anemia - Anemia Life Line
Anaemia Due to Red Cell Loss - BUPA
Anemia - KidsHealth ...
Anemia - Methodist Healthcare System, Houston TX (also in Spanish
Anemia: When Low Iron is the Cause - American Academy of Family Physicians (also in Spanish
Anemia, General - Mayo Clinic
Anemia in Young Women - InteliHealth
Anemias - ...
Women's Health: Anemia - American Institute of Preventive Medicine
Blood Basics
Blood - TeensHealth
Facts About Blood - Methodist Healthcare System, Houston TX
Introduction to Hematology - Puget Sound Blood Center
Red Blood Cells - Puget Sound Blood Center ...
Anemia in Pregnancy
Anemia in Children
About Anemia - KidsHealth
Anemia - KidsHealth
Aplastic Anemia - Lucile Packard Children's Hospital
Hemolytic Anemia - Lucile Packard Children's Hospital ...
Thalassemia
Anemia in Teens
Iron and Teens: A Guide to Anemia Prevention - Children's Hospital, Boston MA

64. ScienceJobs.com - Job Description - Sixteenth Annual International Fanconi Anemi
Job description, Position, Sixteenth Annual International fanconi anemia Scientific Symposium. Organization, The fanconi anemia Research Fund, Inc.
http://www.sciencejobs.com/list/ViewJob-cell3360.html
Home News Jobs Archive ... Subscribe Job description Position Sixteenth Annual International Fanconi Anemia Scientific Symposium Organization The Fanconi Anemia Research Fund, Inc. Location Cambridge, US Massachusetts Date Posted Mar 19 2004 Sixteenth Annual International Fanconi Anemia Scientific Symposium
Hyatt Regency Hotel, Cambridge, MA
October 14 - 17, 2004
Call for Abstracts

The Fanconi Anemia Research Fund, Inc., sponsors its symposium annually to advance the science relating to Fanconi anemia (FA). Sessions include Gene Discovery; Stem Cell Differentiation; Functions of FA Proteins; Solid Tumor Malignancies and Leukemia; Bone Marrow Transplantation; and Novel Therapies. Abstracts for oral or poster presentations must be submitted by June 14, 2004. To receive abstract submission or registration information, send e-mail to info@fanconi.org.
Pilot Study Awards for Research into Fanconi Anemia
The Fanconi Anemia Research Fund, Inc., (Fund) is seeking applications for basic or applied research into the pathogenesis and/or treatment of Fanconi anemia (FA). To develop urgently needed treatments for patients with this disease, a better understanding of molecular pathogenesis in FA is required.
FA is an autosomal recessive disease characterized by bone marrow failure, variable congenital anomalies, and a predisposition to acute myelogenous leukemia and certain epithelial malignancies. FA may have important implications for solid tumor malignancies, such as squamous cell head and neck, gastrointestinal, and gynecological cancers.

65. ScienceJobs.com - Job Description - Sixteenth Annual International Fanconi Anemi
Position, Sixteenth Annual International fanconi anemia Scientific Symposium. Organization, The fanconi anemia Research Fund, Inc.
http://www.sciencejobs.com/viewjob.action?job.id=cell3360&decorator=print

66. Health, Conditions And Diseases, Blood Disorders, Anemia: Fanconi
fanconi anemia Web An informational site for this disorder. fanconi anemia is an inherited anemia which leads to bone marrow failure (aplastic anemia).
http://www.combose.com/Health/Conditions_and_Diseases/Blood_Disorders/Anemia/Fan
Top Health Conditions and Diseases Blood Disorders ... Fanconi
Related links of interest:

67. CAGT - Fanconi Anemia
fanconi anemia. H8713; Phase I/II Study of Allogeneic Stem Cell Transplantation for Patients with Hematologic Malignancy, Using Haploidentical
http://www.bcm.tmc.edu/genetherapy/clinical/fanconi.html
Fanconi Anemia
H8713; Phase I/II Study of Allogeneic Stem Cell Transplantation for Patients with Hematologic Malignancy, Using Haploidentical Family Donors and Sub-Myeloablative Conditioning with Campath 1H: This protocol uses a monoclonal antibody, low dose chemotherapy and radiation in combination with haploidentical allogeneic stem cell transplantation to treat patients with hematologic malignancies who have already received a stem cell transplant or who also have other complications such as kidney, liver, or heart disease.
H8875; Matched Sibling Donor Stem Cell Transplantation for Fanconi Anemia: A Joint Protocol of the FARF and the NMDP: This protocol uses chemotherapy and radiation in combination with a matched allogeneic stem cell transplantation to treat children and adults with Fanconi Anemia.
H9938; CD45 (Yth-24 And Yth-54) and CD52 (Campath-1h) Monoclonal Antibody Conditioning Regimen for HLA-Identical Donor Stem Cell Transplantation of Patients with Fanconi Anemia: This protocol uses monoclonal antibodies in combination with a matched allogeneic stem cell transplantation to treat patients with Fanconi Anemia.

68. Jewish Genetic Diseases Program - What Is A Jewish Genetic Disease
fanconi anemia. fanconi anemia is a chronic blood disorder. Symptoms include Resources fanconi anemia Research Fund, Inc. (FARF) 1801
http://www.sbhcs.com/genetics/offer/fan.html

69. Fanconi Anemia Gene Nomenclature
HGNC Gene Family Nomenclature. fanconi anemia gene nomenclature Definition A fanconi anemia (FA) gene – when mutated at both alleles
http://www.gene.ucl.ac.uk/nomenclature/genefamily/fanconi.html
HGNC Gene Family Nomenclature
Fanconi anemia gene nomenclature Definition
A Fanconi anemia (FA) gene – when mutated at both alleles – causes Fanconi anemia, a rare autosomal recessive disease with diverse symptoms. Because the clinical symptoms vary considerably and/or may be absent altogether, the FA diagnosis depends on a positive chromosomal breakage test in which cells are exposed to a cross-linking agent such as diepoxybutane or mitomycin C. Please click to link below for details of approved symbols Note: an X-chromosome-linked form of FA has not been described in the literature, but can not be excluded theoretically. The gene symbols for FA genes carry the root FANC #, followed by a letter, to be assigned in alphabetical order in order of discovery. If a gene with an existing approved symbol is identified as a FA causing gene, the original gene symbol is usually maintained and an appropriate FANC # gene symbol may be assigned as an alias. Genes encoding proteins that are supposed to function in the FA pathway, but without any patients identified to date who carry mutations in these genes, will have symbols with the root FAAP (for Fanconi anemia associated protein) followed by a number. The number is assigned in order of discovery and reservation is made prior to publication (subject to gene sequence submission) with the HUGO Gene Nomenclature Committee.

70. Fanconi Anemia, Complementation Group D2
You are at Home » Proteins » fanconi anemia, complementation group D2. Suggest a Protein Molecule Authority. fanconi anemia, complementation group D2,
http://www.hprd.org/protein/01968
You are at: Home Proteins Fanconi anemia, complementation group D2
Fanconi anemia, complementation group D2 Cell cycle control protein Cell cycle control protein Cell cycle control protein Regulation of cell cycle Signal transduction ... EXTERNAL LINKS Gene Symbol : Molecular Weight (Da) : Gene Map Locus Localization Primary Nucleus Alternative Domains and Motifs Domains Motifs EXPRESSION Site of Expression Heart Brain Placenta Lung ... Intestine Please send any questions or comments about the Human Protein Reference Database to help@ibioinformatics.org
This is a joint project between: and

71. Fanconi Anemia Group G Protein
You are at Home » Proteins » fanconi anemia group G protein. fanconi anemia group G protein, DNA repair protein. DNA repair protein.
http://www.hprd.org/protein/04262
You are at: Home Proteins Fanconi anemia group G protein
Fanconi anemia group G protein DNA repair protein DNA repair protein Regulation of nucleobase, nucleoside, nucleotide and nucleic acid metabolism ALTERNATE NAMES DISEASES ... EXTERNAL LINKS Gene Symbol : FANCG Molecular Weight (Da) : Gene Map Locus Localization Primary Cytoplasm Alternative Nucleus Domains and Motifs Domains Motifs TPR TPR CC EXPRESSION Site of Expression Spleen Thymus Testis Please send any questions or comments about the Human Protein Reference Database to help@ibioinformatics.org
This is a joint project between: and

72. FANCONI ANEMIA - Meaning And Definition Of The Word
Search Dictionary fanconi anemia Dictionary Entry and Meaning. Medical Dictionary. Definition A rare and often fatal inherited
http://www.hyperdictionary.com/medical/fanconi anemia
English Dictionary Computer Dictionary Thesaurus Dream Dictionary ... Medical Dictionary
Search Dictionary:
FANCONI ANEMIA: Dictionary Entry and Meaning
Medical Dictionary Definition: A rare and often fatal inherited disease in which the bone marrow fails to produce red blood cells, white blood cells, platelets, or a combination of these cells. The disease may transform into myelodysplastic syndrome or leukemia. HOME ABOUT HYPERDICTIONARY

73. Fanconi Anemia (Type C), DNA Analysis
fanconi anemia (Type C), DNA Analysis. Number. Use. Identification of carrier and affected individuals for one mutation associated with fanconi anemia, type C.
http://www.labcorp.com/datasets/labcorp/html/chapter/mono/mg003300.htm
Fanconi Anemia (Type C), DNA Analysis Number CPT Related Information
  • Chromosome Analysis, Instability Syndrome
  • Synonyms Jewish Heritage, IVS+4 A-T Mutation Specimen Whole blood, amniotic fluid, or chorionic villus sample (submission of maternal blood is required for fetal testing) Volume 7 mL Minimum Volume 3 mL Container Lavender-stopper (EDTA) tube; sterile plastic conical tube or two confluent T25 flasks for fetal testing Storage Instructions Maintain specimen at room temperature. Causes for Rejection Frozen specimen; hemolysis; quantity not sufficient for analysis Use Identification of carrier and affected individuals for one mutation associated with Fanconi anemia, type C Limitations Methodology Allele-specific polymerase chain reaction (PCR) and gel electrophoresis References Genet Test , 1997, 1(1):27-33 (review).

    74. Cameron Goodrich's Support Site
    fanconi anemia (FA) is named for a Swiss pediatrician, Guido Fanconi. In 1927 Dr. Fanconi published his clinical observations on
    http://www.totalmayhem.net/cameron/whatisfanconi.htm
    Fanconi Anemia (FA) is named for a Swiss pediatrician, Guido Fanconi. In 1927 Dr. Fanconi published his clinical observations on brothers who had inherited various abnormal physical conditions, and also experienced bone marrow failure. These children suffered severe life-threatening aplastic anemia. Their blood systems could not successfully combat infection, fatigue, spontaneous hemorrhage, or bleeding. Recent research shows these discoveries:
    • FA is one of several deadly inherited anemias
      Both parents must be carriers of a recessive FA gene for their child to be born with this disorder. If both parents carry the recessive gene the chances are one in four that any of their children will inherit the disease.
      FA patients may have a variety of noticeable birth defects, ranging from minor to serious. These defects may affect every major system of the body. Other FA patients are free from any visible disorderother than the ultimate bone marrow failure.
      FA patients experience a high incidence of leukemia (10%-15%).

    75. Short Description Of Cell Lines. Pathology: Fanconi Anemia
    Version 4.200205, Short description of cell lines. Pathology fanconi anemia OMIM Home. By selecting the cell line name, you will
    http://www.biotech.ist.unige.it/cldb/pat32.html
    Version
    Short description of cell lines.
    Pathology: Fanconi anemia
    OMIM Home
    By selecting the cell line name , you will receive the detailed description of the cell line
    By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
    You can search any term of the list by using the 'Find' utility of your browser
    human, Caucasian
    fibroblast GGB
    BD-215
    ...
    By Beatrice...

    76. Short Description Of Cell Lines. Pathology: Fanconi Anemia, Type I *227650
    Version 4.200205, Short description of cell lines. Pathology fanconi anemia, type I *227650 OMIM record. By selecting the cell
    http://www.biotech.ist.unige.it/cldb/pat78.html
    Version
    Short description of cell lines.
    Pathology: Fanconi anemia, type I
    OMIM record
    By selecting the cell line name , you will receive the detailed description of the cell line
    By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
    You can search any term of the list by using the 'Find' utility of your browser
    human, Caucasian
    skin, fibroblast GEIMM
    By Beatrice...

    77. Hopkins Scientists Uncover Role Of Fanconi Anemia Genes In Pancreatic Cancer
    Hopkins Scientists Uncover Role of fanconi anemia Genes in Pancreatic Cancer. The genes have all been associated with fanconi anemia.
    http://www.hopkinsmedicine.org/press/2003/May/030514.htm
    May 14, 2003 MEDIA CONTACT: Valerie Matthews Mehl
    PHONE:
    E-MAIL: mehlva@jhmi.edu Hopkins Scientists Uncover Role of Fanconi Anemia Genes in Pancreatic Cancer
    Scientists at the Johns Hopkins Kimmel Cancer Center have identified three genes, long linked to a rare inherited disease known as Fanconi Anemia (FA), that now appear to play a role in many cases of pancreatic cancer. All of the genes identified, when functioning normally, are part of the DNA repair process. The work is reported in the May 15, 2003, issue of Cancer Research. "What we think we have is a new genetic cause of some cases, approximately 10 percent or more, of pancreatic cancers, one of the most lethal forms of cancer," according to Scott Kern, M.D., professor of oncology and pathology at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins and director of the study. The good news is that these genes offer new targets for improved treatment, he says. The genes have all been associated with Fanconi Anemia. Those affected are born with only a single normal copy of one or more of the genes. Though they do not develop FA, these people often develop pancreatic cancer, usually in their 40s and 50s, about a decade earlier than average age of onset, according to Kern. "The up side is that while these gene mutations cause a horrific disease, they may actually be the Achilles heel of the tumor and make these particular cancers more responsive to treatment," says Kern.

    78. :: Ez2Find :: Fanconi
    Web Sites, Adam Day Site Info - Translate - Open New Window Learn about a boy who passed away after a fight with fanconi anemia.
    http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
    Guide : Fanconi Global Metasearch
    Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode
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    ez2Find Home Directory Health Conditions and Diseases ... Anemia : Fanconi Related Categories Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders
    Web Sites

    79. NewScientistJobs.com - Job Description - Sixteenth Annual International Fanconi
    Position, Sixteenth Annual International fanconi anemia Scientific Symposium. Organization, The fanconi anemia Research Fund, Inc.
    http://www.newscientistjobs.com/list/ViewJob-cell3360.html
    Home News Jobs Archive ... Graduate Job description Position Sixteenth Annual International Fanconi Anemia Scientific Symposium Organization The Fanconi Anemia Research Fund, Inc. Location Cambridge, US Massachusetts Date Posted 19 Mar 2004 Sixteenth Annual International Fanconi Anemia Scientific Symposium
    Hyatt Regency Hotel, Cambridge, MA
    October 14 - 17, 2004
    Call for Abstracts

    The Fanconi Anemia Research Fund, Inc., sponsors its symposium annually to advance the science relating to Fanconi anemia (FA). Sessions include Gene Discovery; Stem Cell Differentiation; Functions of FA Proteins; Solid Tumor Malignancies and Leukemia; Bone Marrow Transplantation; and Novel Therapies. Abstracts for oral or poster presentations must be submitted by June 14, 2004. To receive abstract submission or registration information, send e-mail to info@fanconi.org.
    Pilot Study Awards for Research into Fanconi Anemia
    The Fanconi Anemia Research Fund, Inc., (Fund) is seeking applications for basic or applied research into the pathogenesis and/or treatment of Fanconi anemia (FA). To develop urgently needed treatments for patients with this disease, a better understanding of molecular pathogenesis in FA is required.
    FA is an autosomal recessive disease characterized by bone marrow failure, variable congenital anomalies, and a predisposition to acute myelogenous leukemia and certain epithelial malignancies. FA may have important implications for solid tumor malignancies, such as squamous cell head and neck, gastrointestinal, and gynecological cancers.

    80. Research On Fanconi Anemia
    fanconi anemia. Sectie Functionele Genoomanalyse. With the 1992 landmark publications by Manuel Buchwald s group in Toronto reporting
    http://www.med.vu.nl/kga/ondz_fanc.html
    Fanconi anemia Sectie Functionele Genoomanalyse With the 1992 landmark publications by Manuel Buchwald's group in Toronto reporting 4 complementation groups (in 7 FA patients) and expression cloning of the first FA gene ( FANCC ) we decided to embark on the genetic approach. Thus, after a 3-months sabbatical in Buchwald's laboratory (H.J.) a collaborative research line was initiated aiming at extended complementation studies and gene cloning. In addition, we initiated and participated in a EU-sponsored Concerted Action EUFAR (1994 -1996) which allowed us to establish a Cell Repository for cell material from FA patients diagnosed in European countries and elsewhere. This facility enabled us to carry out complementation analysis on patients from diverse ethnic backgrounds, which led to the recognition of 8 complementation groups, mapping of the FANCA gene and cloning of FANCA, FANCG, FANCF

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