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ZAP-70 Ab-1(clone 2F3.2)
1, Issue 2: featuring Gowna€™s article on SP1 and SP3, IHC Standardization, and more Comprehensive Breast Panel available now.
Mouse Monoclonal Antibody Description: Mutations in ZAP-70 gene results in a form of Severe Combined Immunodeficiency Syndrome (SCID) in humans.
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p57 Kip2^ Ab-7
The gene encoding human p57Kip2 is located on chromosome 11p15.5, a region implicated in both sporadic cancers, Wilm's tumor, and Beckwith-Wiedemann syndrome (BWS), a cancer syndrome, making it a tumor suppressor candidate.
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p57 Kip2^ Ab-6
The gene encoding human p57Kip2 is located on chromosome 11p15.5, a region implicated in both sporadic cancers, Wilm's tumor, and Beckwith-Wiedemann syndrome (BWS), a cancer syndrome, making it a tumor suppressor candidate.
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p57 Kip2^ Ab-3
The gene encoding human p57Kip2 is located on chromosome 11p15.5, a region implicated in both sporadic cancers, Wilm's tumor, and Beckwith-Wiedemann syndrome (BWS), a cancer syndrome, making it a tumor suppressor candidate.
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Microphthalmia (Transcription Factor) (MiTF).
1, Issue 2: featuring Gowna€™s article on SP1 and SP3, IHC Standardization, and more Comprehensive Breast Panel available now.
The mutation of Mi causes Waardenburg Syndrome type II in humans.
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Microphthalmia (Transcription Factor) (MiTF) Ab-2
1, Issue 2: featuring Gowna€™s article on SP1 and SP3, IHC Standardization, and more Comprehensive Breast Panel available now.
The mutation of Mi causes Waardenburg Syndrome type II in humans.
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Microphthalmia (Transcription Factor) (MiTF) Ab-1
The mutation of Mi causes Waardenburg Syndrome type II in humans.
Microphthalmia (Transcription Factor) (MiTF) Ab-1 Microphthalmia (Transcription Factor) (MiTF) Ab-1 antibody, IHC, immunohistology antibody, IHC, immunohistology.
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Amyloid A4 / Amyloid Beta.
1, Issue 2: featuring Gowna€™s article on SP1 and SP3, IHC Standardization, and more Comprehensive Breast Panel available now.
Beta amyloid deposits are also detected in Lewy-body dementia, Downa€™s syndrome, amyloidosis (Dutch type) and in the Guam Parkinson-Dementia complex.
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Amyloid A4 / Amyloid Beta Ab-1
Beta amyloid deposits are also detected in Lewy body dementia, Downa€™s syndrome, amyloidosis (Dutch type) and in the Guam Parkinson-Dementia complex.
Amyloid A4 / Amyloid Beta Ab-1 Amyloid A4 / Amyloid Beta Ab-1 antibody, IHC, immunohistology antibody, IHC, immunohistology.
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14.3.3 gamma Ab-2
1, Issue 2: featuring Gowna€™s article on SP1 and SP3, IHC Standardization, and more Comprehensive Breast Panel available now.
In Alzheimera€™s disease and Down syndrome level of 14.3.3 gamma in brain increases significantly.
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Lab Vision Corporation, a part of Thermo Fisher Scientific
PTM TM : an integrated solution for any Autostainer for dewaxing and HIER Literature Catalog Brochures & Flyers Articles & References -Tutorial Center -- -Search:- - - Account Login - View Shopping Cart ZAP-70 Ab-1(clone 2F3.2) Click here to view IVD datasheet Mouse Monoclonal Antibody Description: Mutations in ZAP-70 gene results in a form of Severe Combined Immunodeficiency ...
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Lab Vision Corporation, a part of Thermo Fisher Scientific
1, Issue 2: featuring Gowna€™s article on SP1 and SP3, IHC Standardization, and more Comprehensive Breast Panel available now.
Beta amyloid deposits are also detected in Lewy-body dementia, Downa€™s syndrome, amyloidosis (Dutch type) and in the Guam Parkinson-Dementia complex.
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http://www.jax.org/alstrom/slo98/thumb1.html
Supporting those affected by AlstrA¶m Syndrome --- General information --- AlstrA¶m Syndrome International -------•- About ASI -------•- What's New at ASI -------•- ASI Conferences -------•- How you can help -------•- Countries Served by ASI -------•- Board of Directors -------•- Scientific Advisory Board --- For Families -----...
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Alstroem Syndrome International Family Conference and Clinic Ontario, Canada 2001
Home 1 2 TD class=tableborderzero width="33%"> 1 2 3 TD class=tableborderzero width="33%"> 4 5 6 TD class=tableborderzero width="33%"> 7 8 9 TD class=tableborderzero width="33%"> 10 11 12 Home 1 2 Return to Third International Alstrom Syndrome Reunion.
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Second International Alstroem Syndrome Reunion Snapshots
Supporting those affected by AlstrA¶m Syndrome --- General information --- AlstrA¶m Syndrome International -------•- About ASI -------•- What's New at ASI -------•- ASI Conferences -------•- How you can help -------•- Countries Served by ASI -------•- Board of Directors -------•- Scientific Advisory Board --- For Families -----...
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First International Alstrom Syndrome Reunion
TD class=tableborderzero width="33%"> 1 2 3 TD class=tableborderzero width="33%"> 4 5 6 TD class=tableborderzero width="33%"> 7 8 9 TD class=tableborderzero width="33%"> 10 - 11 - Home - General Information - Alstr A¶m Syndrome International For Families - For Professionals Last Modified: October 31, 2008-- First International Alstrom Syndrome Reunion First...
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- - The Jackson Laboratory
By testing DNA samples of patients with Alstroem syndrome and comparing them to samples from the general human population, the scientists isolated a gene, ALMS1, which is mutated in the Alstroem patients.- The function of the protein encoded by ALMS1- remains unclear.
Statistically, if two adults each have one mutated gene, there is a 1-in-4 likelihood that a child of...
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- The Jackson Laboratory
Genetic resources & information JAX® Mice and Services Find JAX ® Mice Ordering information JAX ® Services Technical support & literature Animal health & genetic quality Research affiliates program Shortcuts for researchers Mouse Genome Informatics (MGI) Search for JAX® Mice Mouse Phenome Database More resources International Mouse Strain Resources (IMSR) Knockout...
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2002 Archived Media Releases - The Jackson Laboratory
2007 News Archive 2006 News Archive 2005 News Archive 2004 News Archive 2003 News Archive 2002 News Archive 2002 Archived Media Releases - December 2002 New Mouse Genome Sequence Draft Means Boost for Jackson Laboratory Research November 2002 Jackson Laboratory Summer Student Competes at MIT September 2002 Jackson Laboratory researchers identify a gene implicated in oxidative stress...
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Spontaneous mutations characterized by the MMR - The Jackson Laboratory
- Gene/Allele Symbol Allele Name ank progressive ankylosis Ap3b1-pe- pearl Ap3d-mh- mocha Ar-Tfm- testicular feminization Atp7a-Mo-br- brindled Atp7b-tx-J- toxic milk Jackson Cacna1a-tg- tottering Cacnb4-lh- lethargic Cdh23-v-2J- waltzer 2 Jackson Chx10-or-J- ocular retardation Jackson Clcn1-adr-mto- myotonia Cln6-nclf- neuronal ceroid lipofuscinosis Col1a2-oim- osteogenesis...
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New Gene Mutations - The Jackson Laboratory
Mutation Symbol Mutation Name Gene Symbol Phenotype Chr bdd bulging disc disease skeletal 2 Trl Trembler-like neurological 11 trls-2J tremor and reduced lifespan 2 Jackson neurological 10 agil-2J agitans-like 2 Jackson neurological 14 twi-5J twitcher 5 Jackson Galc neurological 12 Mfs mutant fur is striped skin and hair 13 fsq flying squirrel neurological 10 dkd darkened dorsal skin...
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The Jackson Laboratory media and museum collection: Videotape - The Jackson Laboratory
'96 - Channel 5 boxed 76-51 Made in Maine - TJL - WCBB - TV 10 boxed 77-52 Genes and cancer 1993 - - - boxed 78-53 - - - Interior of mouse rooms In house boxed 79-54 The mouse as a model organism 1995 Shirley Tishman (1995) - - boxed 80-55 Obesity research at TJL - Ed Leiter - CBS- boxed 81-56 Ob Gene - - Various clips, 2nd copy - boxed 82-57 Annual Meeting 1993 - - In house...
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- The Jackson Laboratory
rd3 was proposed as a candidate gene for orthology to human USH2A (OMIM 276901), which causes a mild form of Usher syndrome deafness.
Gene Mouse Chromosome Human Chromosome Retinal ONL disappear by Strains rd3 1 1q32 4 RBF/DnJ; Rb4Bnr/DnJ; RBJ/DnJ; IN30/Rk Back to genetic resources In this section Eye Mutant Resource Retinal degeneration genes Cataracts Other Mouse...
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Mutations Causing Inner Ear Dysfunction - The Jackson Laboratory
(2006) PLoS Genet 2:Epub Eya1 eyes absent 1 homolog (Drosophila) 1 10 bor branchio-oto-renal syndrome homolog sp, tm inner ear development Johnson et al.
Ush2a Usher syndrome 2A homolog (human) 1 106 KO targeted inactivation tm outer hair cell loss in basal cochlea Liu et al.
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Genetic modifiers of hearing - The Jackson Laboratory
and Noben-Trauth, K., The Mass1(frings) mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC, Genomics, 85 (2005) 582-90.
and Roux, A.F., A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?, Eur J Hum Genet, 10 (2002) 72-6.
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