61. BBS4: Bardet-Biedl Syndrome 4(Protein Catalog) - [Abnova Corporation] Protein Catalog ‡ For research use only, not for resale. BBS4 bardetbiedl syndrome 4. Human recombinant protein (Wheat Germ). http://www.abnova.com.tw/Content/en/Product/ProdCata.asp?ID=H00000585-P01

62. OMIM - #209900 BARDET-BIEDL SYNDROME; BBS 209900 bardetbiedl syndrome; BBS. Alternative titles; symbols. BARDET 30 MEDLINE Neighbors. bardet-biedl syndrome 1. Beales et al. (1997 http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=209900

63. Entrez PubMed Click here to read Identification of a novel bardetbiedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?holding=npg&cmd=Retrieve&db=PubMed

64. Bardet-Biedl Syndrome From Linkspider UK Health Directory Directory Topic bardetbiedl syndrome assoicated to Health. National Library of Medicine - A summary of bardet-biedl syndrome and a list of major features. http://linkspider.co.uk/Health/ConditionsandDiseases/NeurologicalDisorders/Brain

Match » -All words -Any word -Exact text Search » The Web Jobs / Vacancy Images / Photos FTP / Downloads United Kingdom United States of America Argentina Austria Australia Bangladesh Belgium Bolivia Brazil Bulgaria Canada Chile China Cuba Cyprus Czech Republic Czechoslovakia Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Ghana Greece Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Jordan Kenya Kuwait Latvia Lithuania Luxembourg Malaysia Malta Mexico Moldavia Monaco Morocco Mozambique Nepal Netherlands New Zealand Nicaragua Nigeria North Korea Norway Pakistan Panama Paraguay Peru Philippines Poland Portugal Qatar Romania Russian Federation Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates Uruguay Venezuela Yemen Yugoslavia Zambia Zimbabwe Ranking » On (no duplicate) Off (allow duplicate) Add my Site Toolbar Affiliates Directory Topic Bardet-Biedl Syndrome assoicated to Health Directory Tree: Top Health Conditions and Diseases Neurological Disorders ... Brain Diseases : Bardet-Biedl Syndrome ( See Also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders National Library of Medicine - A summary of Bardet-Biedl syndrome and a list of major features.

65. Ask NOAH About: The Eye The Aniridia Network Anopthalmia Movements Online Aphakia - Texas School for the Blind and Visually Impaired bardet-biedl syndrome bardet-biedl syndrome http://www.noah-health.org/english/illness/eye/eye.html

Ask NOAH About: The Eye Common Eye Health Topics Care and Treatment Basic Eye Information Basic Anatomy Normal Vision Optical Illusions ... Social Resources Related Concern Information Resources Eye Care Special Concerns Clinical Trials and New Medications Enucleation and Orbital Implants Eye Health and Safety ... Research Common Eye Health Topics Basic Eye Information Anatomy Eye Anatomy - Phillips Eye Institute Physical Structures of the Eye - Univ of Pennsylvania Glossary - Boston University Glossary of Eye Terminology - Methodist Health Care System, Houston TX (also in Spanish The Eyes (Complete Home Medical Guide/Columbia University Heredity of Eye Color - McGraw Hill How We See Things That Move - Howard Hughes Medical Institute, Chevy Chase, MD ... What Is the Blind Spot? - Serendip Normal Vision 20/20 Vision - American Optometric Association (AOA) Find good habits for good eyes - American Association of Retired Persons Infants' Vision - American Optometric Association (AOA) Your School-age Child's Eyes - American Optometric Association (AOA) ... Vision Changes During Pregnancy - BabyZone Optical Illusions Fading Dot - The Exploratorium, San Francisco CA

66. »»Reviews For Bardet-Biedl Syndrome«« bardetbiedl syndrome Reviews. Related Subjects Brain_Diseases More Pages bardet-biedl syndrome Page 1 2 3. Search site for a Book Review. http://www.booksunderreview.com/Health/Conditions_and_Diseases/Neurological_Diso

Bardet-Biedl Syndrome Reviews Related Subjects: More Pages: Bardet-Biedl Syndrome Page 1 Book reviews for "Bardet-Biedl Syndrome" sorted by average review score: Sindrome de Fatiga Cronica Published in Paperback by Editorial Libra (30 July, 1994) Authors: Jorge, Dr Escalante, Dr Jorge Octavio Escalante, and Doctor Jorge Octavio Escalante Amazon base price: Average review score: A VECES SOSPECHO QUE, COMO EN EL CASO DE LOS VIRUS DE LAS COMPUTARODORAS, ALGUIEN O VARIOS SERES MONSTRUOSOS JUEGAN CON NUESTRA VIDA DESDE LOS LABORATORIOS MEDICOS... De otra manera,¿C“MO TE EXPLICAS LA EPIDEMIA DE EPIDEMIAS? Y LA FASTIGA CRONICA ESTA CAUSADA POR EL VIRUS DE EPSTEIN BARR... Y NO EXISTIA... Pero esa LA PUEDES DETECTAR Y COMBATIR..NO DEJES QUE SE TE CONFUNDA CON DEPRESION, O QUE UN MEDICO IGNORANTE LA CALIFIQUE COMO TAL... PREVENTE ! ESTAMOS VIVIENDO EN LA "ERA DE LAS EPIDEMIAS ": Primero, EL SIDA Luego, EL ‰BOLA AHORA, LA PULMONA ATPICA Pero todo el tiempo, como agazapado en la oscuridad, EL SFC (Sindrome de Fatiga Cr³nica ), que da±a tanto PORQUE NO SE DETECTA FCILMENTE...Y QUE CRECE DA POR DIA COMO TODO LOS ORIGINADO POR UN VIRUS! Es el caso de la Pulmon­a At­pica, que se confunde con una bronquitis o una gripa fuerte... En el caso de la Fatiga Cr³nica, tenemos el recurso de ESTE ESTUPENDO LIBRO QUE NOS MUESTRA LOS SNTOMAS Y EL CAMINO A SEGUIR..

67. MGI 2.98 - Marker Detail 2.98. Gene Detail, Symbol Name ID, Bbs7 bardetbiedl syndrome 7 MGI1918742, Nomenclature History. Synonyms, 8430406N16Rik. Map position, http://www.informatics.jax.org/searches/accession_report.cgi?id=MGI:1918742

68. PillSupplier.com - Conditions And Diseases/Neurological Disorders/Brain Diseases Category bardetbiedl syndrome. HOME Conditions and Diseases/Neurological Disorders/Brain Diseases/bardet-biedl syndrome. Links Laurence http://www.pillsupplier.com/dir/432/

Category: Bardet-Biedl Syndrome HOME ABOUT US ORDER STATUS BMI CALCULATOR ... CONTACT US Prescription Drugs Diet Pills Adipex Bontril Didrex ... Login Conditions and Diseases/Neurological Disorders/Brain Diseases/Bardet-Biedl Syndrome Links: Laurence-Moon-Bardet-Biedl Syndrome Network [rate it] [review it] Raises public awareness of the Laurence-Moon Bardet-Biedl syndrome and serves as a place for parents of LMBBS children to meet and exchange ideas. National Library of Medicine [rate it] [review it] A summary of Bardet-Biedl syndrome and a list of major features. NORD - Bardet Biedl Syndrome [rate it] [review it] Offers a general discussion along with further resources. Readers Digest Health [rate it] [review it] Bardet-Biedl syndrome: General information and resources. The CaF Directory [rate it] [review it] Information about Laurence-moon-bardet-biedl syndrome, its symptoms and inheritance patterns. UMDS: LMBBS [rate it] [review it] Information for health-care professionals involved in the care of Laurence-Moon-Bardet-Biedl Syndrome patients and for parents or relatives seeking education on the syndrome. Search Looking for something in particular?

69. MKKS CM010920, 32, ATTgATG, Ile-Met, bardet-biedl syndrome, 1. CM002360, 52, GGT-GAT, Gly-Asp, bardet-biedl syndrome, 3. CM002361, 57, aACC-GCC, Thr-Ala, bardet-biedl syndrome, 4. http://www.uwcm.ac.uk/uwcm/mg/ns/1/9860197.html

MKKS Nucleotide substitutions (missense / nonsense) Accession Number Codon Nucleotide Amino acid Phenotype Reference ATTg-ATG Ile-Met Bardet-Biedl syndrome TAT-TGT Tyr-Cys McKusick-Kaufman syndrome GGT-GAT Gly-Asp Bardet-Biedl syndrome aACC-GCC Thr-Ala Bardet-Biedl syndrome tCAT-TAT His-Tyr McKusick-Kaufman syndrome tCAG-TAG Gln-Term Bardet-Biedl syndrome CGT-CTT Arg-Leu Bardet-Biedl syndrome aTCA-CCA Ser-Pro Bardet-Biedl syndrome gGCA-TCA Ala-Ser McKusick-Kaufman syndrome TATg-TAA Tyr-Term Bardet-Biedl syndrome CTT-CCT Leu-Pro Bardet-Biedl syndrome GAC-GCC Asp-Ala Bardet-Biedl syndrome aATA-GTA Ile-Val Bardet-Biedl syndrome GGA-GAA Gly-Glu Bardet-Biedl syndrome TGT-TCT Cys-Ser Bardet-Biedl syndrome gTCT-GCT Ser-Ala Bardet-Biedl syndrome CGT-CAT Arg-His Bardet-Biedl syndrome References 1 - Beales (2001) Am J Hum Genet 2 - Stone (2000) Nat Genet ... Hum Genet HGMD

70. Mutations In The Worm Orthologue Of The Bardet-Biedl Syndrome Gene BBS7 Produce Program Nr 414C Mutations in the worm orthologue of the bardetbiedl syndrome gene BBS7 produce sensory neuron dysfunction. Mark http://genetics.faseb.org/genetics/Celegans/2003abs/f414C.htm

Program Nr: Mutations in the worm orthologue of the Bardet-Biedl Syndrome gene BBS7 produce sensory neuron dysfunction. Mark Audeh , Mike Reardon, Stephen R. Wicks. Biology, Boston College, Chestnut Hill, MA. Bardet-Biedl Syndrome is a rare genetic disorder characterized by progressive retinal degeneration similar to retinitis pigmentosa. Patients can also suffer from obesity, polydactyly, hypogenitalism, mental retardation and renal malformations. In humans, the gene BBS7 has been implicated in this disorder. The BBS7 gene is an orthologue of C. elegans gene Y75B8A.12. osm-12 was isolated in screens for worms defective osmotic avoidance while retaining an intact amphid organ, as determined by dye filling. We have adapted the osmotic avoidance assay developed by Jim Thomas in order to further characterize the Osm-12 phenotype. Weve cloned osm-12 . It corresponds to the BBS7 orthologue Y75B8A.12. Notably, osm-12 has an RFX-box in the proximal promoter, and this element has been shown to drive expression of target genes in sensory neurons. To verify this predicted expression pattern, we are generating antibodies to OSM-12, and are injecting a GFP transcriptional fusion of the osm-12 promoter.

71. ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page Version pour Impression, MALADIE bardet-biedl, syndrome de, Maladie(s) incluse(s) bardet-biedl type 1, syndrome de bardet-biedl http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=110

72. ORPHANET® : Bardet-Biedl, Syndrome De bardet-biedl type 2, syndrome de; bardet-biedl type 3, syndrome de; http://www.orpha.net/static/FR/bardetbiedl.html

Accès à la base de données Orphanet Bardet-Biedl, syndrome de Accès direct aux détails Alias Bardet-Biedl type 1, syndrome de Bardet-Biedl type 2, syndrome de Bardet-Biedl type 3, syndrome de Bardet-Biedl type 4, syndrome de Bardet-Biedl type 5, syndrome de Bardet-Biedl type 6, syndrome de Bardet-Biedl type 7, syndrome de Résumé Le syndrome de Bardet-Biedl est une maladie génétique autosomique récessive qui associe une obésité, une rétinite pigmentaire, une hexadactylie postaxiale, un hypogénitalisme, une atteinte rénale et un retard mental très variable et souvent modéré. Le traitement est uniquement symptomatique. Il existe une grande hétérogénéité génétique puisque 8 gènes responsables de cette affection ont été localisés ; 6 de ces gènes sont identifiés. Le diagnostic prénatal par la biologie moléculaire ou par la biochimie n'est réalisable que si la mutation d'un cas index a été identifiée ; ces tests ne sont cependant pas effectués en pratique courante. *Auteur : Pr D. Bonneau (octobre 2003)*. Texte(s) long(s) http://www.orpha.net/data/patho/FR/fr-BBS.pdf

73. Bardet-Biedl, Syndrome : Arborescences MeSH Translate this page bardet-biedl, syndrome arborescences MeSH. Menu général CISMeF. Vous pouvez aussi consulter toutes les arborescences des mots http://www.chu-rouen.fr/navimesh/B/navibardetbiedlsyndrome.html

Bardet-Biedl, syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF système nerveux, maladies système nerveux central, maladies encéphalopathies hypothalamus, maladies ... Zellweger, syndrome 07 janvier 2004 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

74. Syndrome Of Bardet-Biedl bardetbiedl s syndrome. Health has no price Obesidad.net is educational Visit us continually. You bardet-biedl S syndrome. Bardet http://www.obesidad.net/english2002/disorder9.shtml

Bardet-Biedl's syndrome Health has no price Obesidad.net is educational Visit us continually. You will always find new advice for your health. Recommend this site. Recommend this site to a friend or relative who may find it helpful BARDET-BIEDL'S SYNDROME Bardet-Biedl's syndrome is a hereditary disease that affects many parts of the body. Obesity, the pygmentary retinitis (night blindness and the progressive loss of the peripheral vision), the mental delay, the hypogonadism, the renal damage and the polydactylia (fingers extra in the feet), define the characteristics of Bardet-Biedl's syndrome. INHERITANCE Two forms have been identified: Bardet-Biedl's syndrome 1, which does not have relation with the chromosome 16. Bardet-Biedl's syndrome 2, that has relation with the chromosome 16. Bardet-Biedl's syndrome is transmitted genetically across the families by inheritance autosomic recessive. In this type of inheritance, both parents are called carriers, they have a gene of the syndrome paired with a normal gene. Each of his children have at the time a possibility of 25% (or an opportunity in four) of inheriting both Bardet-Biedl's genes (one of every father) necessary to cause this disease. The carriers are healthy because only they have a copy of the gene. At this moment, it is impossible to determine if someone is a carrier of Bardet-Biedl's syndrome but until the birth of an affected child.

75. BARDET-BIEDL (LAURENCE-MOON-BARDET-BIEDL) SYNDROME Features Listed For bardetbiedl (LAURENCE-MOON-bardet-biedl) syndrome. McKusick 209900. Abnormal liver (including function); Biliary http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?154

76. Sindrome Laurence Moon Bardet Biedl Syndrome Bambi Sindrome Laurence Moon Bardet Biedl syndrome Bambi http://antares.fastnet.it/enti/bambi/sindrome-laurence-moon-bardet-biedl.htm

Sindrome di Laurence Moon Bardet Biedl Laurence Moon Bardet Biedl http://www.rpitalia.org/riabilitazione_sanpaolo.htm http://www.5mcc.com/SUMMARY/0519.html http://www.lmbbs.org.uk http://home.talkcity.com/OceanBlvd/iamahawkfan/bardetbeidlsyndrome.html ... http://rarediseases.about.com/health/rarediseases/cs/bardetbiedlsynd/index.h tm http://www.patient.co.uk/illness/l/laurence_moon_bbs.html http://hjem.get2net.dk/ole_jorgensen http://www.healthfinder.gov/text/docs/doc04525.htm http://www.laurushealth.com/Library/HealthGuide/SelfHelp/_followlink.asp?sgm ... http://www.bis.med.jhmi.edu/Dan/kidbase/bardetbiedl/bardetbiedl-help.html BAMBI -INFORMAZIONI SULLE MALATTIE RARE DEI BAMBINI- E' ON LINE DAL 1997 E-mail ruffelli@tin.it

77. Ingenta: Article Summary -- Prenatal Diagnosis Of Bardet-Biedl Syndrome By Targe Prenatal diagnosis of Bardet–Biedl syndrome by targeted secondtrimester sonography Ultrasound in Obstetrics Gynecology April 2001, vol. 17, no. 4, pp. http://www.ingenta.com/isis/searching/ExpandTOC/ingenta?issue=pubinfobike://bsc/

78. Laurence Moon Bardet Biedl Syndrome Lauurence Moon Bardet Biedl syndrome Resources, international support groups, clinics, genetic counselors and geneticists http://www.kumc.edu/gec/support/laurmoon.html

Laurence Moon Bardet Biedl Syndrome Laurence Moon Bardet Biedl Syndrome Network Laurence-Moon-Bardet-Biedl Syndrome , Canada Laurence-Moon-Bardet-Biedl Syndrome (LMBBS) , Molecular and Medical Genetics, Prince Philip Research Laboratories, Guy's Hospital London Laurence-Moon Syndrome , Pediatric Database (PEDBASE) Laurence-Moon-Bardet-Biedl (LMBB) , Senter for sjeldne sykdommer og syndromer Smågruppesenteret på Rikshospitalet Centre for Rare Disorders Laurence-Moon-Bardet-Biedl Society , United Kingdom Bardet-Biedl Laurence-Moon Syndrome , Belgium or Dutch LMBBS discussion group,(Laurence Moon Baardet-Beidl Syndrome) , Australia Syndrome de Laurence-Moon-Bardet-Biedl France Laurence-Moon Syndrome , Online Mendelian Inheritance in Man (OMIM) #245800 Bardet-Biedl Syndrome (BBS) , Online Mendelian Inheritance in Man (OMIM) Laurence Moon , signs of condition, Orphanet Laurence-Moon-Bardet-Biedl Syndrome , WideSmiles Also See: National organizations information on genetic conditions or birth defects Information for siblings and family members , genetic conditions Vision Impairment / Blindness Resources To locate a genetic counselor or clinical geneticist in your area: Professional Genetics Societies Genetic clinics, centers, departments

79. Bardet Biedl Syndrome (BBS) Links to information and resources for Laurence Moon syndrome/Bardet Biedl syndrome, a genetic disorder of chromosomes 16, 3, and 15. Foundation Fighting Blindness Bardet Biedl. Good information http://rarediseases.about.com/cs/bardetbiedlsynd

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Home Essentials ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Bardet Biedl Syndrome/Laurence Moon Synd Guide picks A genetic disorder of chromosomes 16, 3, and 15 which causes progressive blindness, obesity, extra fingers and toes, and mental retardation. Howard Hughes Medical: Bardet Biedl Article on the discovery of the gene for Bardet Biedl Syndrome, from the Howard Hughes Medical Institute. Laurence-Moon-Bardet-Biedl Society Site provides information, news, research, and support for Laurence Moon Bardet Biedl Syndrome. NORD: Bardet Biedl Syndrome Brief definition of Bardet Biedl Syndrome, from the National Organization for Rare Disorders (NORD). NORD: Laurence Moon Syndrome Brief definition of Laurence Moon Syndrome, from the National Organization for Rare Disorders (NORD).

80. Laurence Moon/Bardet Biedl Syndrome Laurence Moon/ Bardet Biedl syndrome. LMBBS Home page This page is aimed primarily at medical and healthcare professionals involved http://www.lowvision.org/laurence_moon.htm

Laurence Moon/ Bardet Biedl Syndrome LMBBS Home page This page is aimed primarily at medical and health-care professionals involved in the care of LMBBS patients and also for parents or relatives wishing to know more about the syndrome and the implications for those affected. LMBBS Home page This page is aimed primarily at medical and health-care professionals involved in the care of LMBBS patients and also for parents or relatives wishing to know more about the syndrome and the implications for those affected.

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