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master_table - The Jackson Laboratory
KO - tm semicircular canal defects [253] Ntf3 neurotrophin 3 6 61 KO - tm hair cell innervation [86, 92, 99] Ntn1 netrin 1 U - KO - tm semicircular canal formation; homozygous lethal [270] Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 13 36 KO - tm hair cell innervation [98, 276] - homozygous lethal Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 7 39 KO - tm hair cell...
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M:\Printing\Categories\Adrenergics\adrenrevpdf1.cdr
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author: janec
updated: 23/11/2002
matching:
langer syndrom chromosom
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600500.DOC
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author: Sean
updated: 09/02/2006
matching:
langer chromosom region
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MMCC Results / April 1998
Illinois] Proteins 30, 113-135 (1998) The HMG-box portion of several chromosomal proteins binds to the minor groove of bent DNA and is thought to facilitate binding of other transcription factors to repress or facilitate gene expression.
Langer.
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COL2A1 Recombinant Protein (P01)-Abnova Corporation
Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type.
author: Abnova
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Bachem_UG_01_d
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author: birki.onevision
updated: 17/03/2006
matching:
langer syndrom
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M:\Printing\Categories\Adrenergics\adrenrevpdf1.cdr page 4
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author: janec
updated: 23/11/2002
matching:
langer syndrom
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Accelrys: Scientific References: Accelrys Staff Papers 2000 - present
Laggner, C., Schieferer, C., Fiechtner, B., Poles, G., Hoffmann, R., Glossmann, H., Langer, T., Moebius, F., Discovery of High Affinity Ligands of sigma1 receptor, ERG2 and EBP by Pharmacophore Modeling and Virtual Screening J.
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600300.DOC
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author: KBOMYSOA
updated: 09/02/2006
matching:
langer chromosom
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Microsoft Word - BMS216CERev03.doc
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author: hummel
updated: 22/12/2005
matching:
langer chromosom
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Microsoft Word - BMS216_INSTRev06.doc
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author: hummel
updated: 07/10/2005
matching:
langer chromosom
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Microsoft Word - BMS216_Rev05.doc
...
author: jaksits
updated: 30/09/2005
matching:
langer chromosom
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Microsoft Word - 216MST_Rev04.doc
...
author: jaksits
updated: 10/06/2005
matching:
langer chromosom
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Microsoft Word - BMS216INSTCERev04.doc
...
author: jaksits
updated: 10/02/2005
matching:
langer chromosom
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CECR5 Recombinant Protein (P01)-Abnova Corporation
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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WHSC2 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4.
This gene is mapped to the 165 kb WHS critical region, and may play a role in the phenotype of the WHS or Pitt-Rogers-Danks syndrome.
author: Abnova
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TSSC1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer.
Alignment of this gene to genomic sequence data suggests that this gene may reside on chromosome 2 rather than chromosome 11.
author: Abnova
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SHMT1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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ATXN2 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes.
ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders.
author: Abnova
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NOS2A Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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LLGL1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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NSD1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome.
One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorac domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11.
author: Abnova
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NCOR1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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SREBF1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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GNB1L Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes.
The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye ...
author: Abnova
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