Chromosome 9

Common Name(s)

Chromosome 9

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 9" for support, advocacy or research.

Chromosome 9 Disorder Advocates

Changing the world one chromosome and one hope at a time. We are your voice and your direction if ever you feel speechless or lost.

Last Updated: 3 Aug 2016

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General Support Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 9" for support, advocacy or research.

Chromosome 9 Disorder Advocates

Changing the world one chromosome and one hope at a time. We are your voice and your direction if ever you feel speechless or lost.

http://www.facebook.com/9qdeletion

Last Updated: 3 Aug 2016

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General Support Organizations

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General Resources

46,XY,del(9)(q31.2q33.1)

Single case chromosome disorder in 9

Updated 27 Nov 2013

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Chromosome 9" returned 194 free, full-text research articles on human participants. First 3 results:

High-resolution mapping of a novel rat blood pressure locus on chromosome 9 to a region containing the Spp2 gene and colocalization of a QTL for bone mass.
 

Author(s): Ying Nie, Sivarajan Kumarasamy, Harshal Waghulde, Xi Cheng, Blair Mell, Piotr J Czernik, Beata Lecka-Czernik, Bina Joe

Journal: Physiol. Genomics. 2016 06;48(6):409-19.

 

Through linkage analysis of the Dahl salt-sensitive (S) rat and the spontaneously hypertensive rat (SHR), a blood pressure (BP) quantitative trait locus (QTL) was previously located on rat chromosome 9. Subsequent substitution mapping studies of this QTL revealed multiple BP QTLs ...

Last Updated: 31 Dec 1969

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B-cell Acute Lymphoblastic Leukemia With t(9;22)(q34;q11) Translocation and Clonal Divergence Through ider(22) Chromosome and t(13;17)(q14;q25) Translocation.
 

Author(s): Juan Pablo Meza-Espinoza, Enrique Jhonatan Romo Martínez, Lilia Aguilar López, Verónica Judith Picos Cárdenas, María Teresa Magaña Torres, Juan Ramón González García

Journal: Ann Lab Med. 2016 Mar;36(2):185-7.

 

Last Updated: 31 Dec 1969

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Pericentric Inversion of Human Chromosome 9 Epidemiology Study in Czech Males and Females.
 

Author(s): A Šípek, A Panczak, R Mihalová, L Hrčková, E Suttrová, V Sobotka, P Lonský, N Kaspříková, V Gregor

Journal: Folia Biol. (Praha). 2015 ;61(4):140-6.

 

Pericentric inversion of human chromosome 9 [inv(9)] is a relatively common cytogenetic finding. It is largely considered a clinically insignificant variant of the normal human karyotype. However, numerous studies have suggested its possible association with certain pathologies, e.g., ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Chromosome 9" returned 4 free, full-text review articles on human participants. First 3 results:

Insights into the pathogenic mechanisms of Chromosome 9 open reading frame 72 (C9orf72) repeat expansions.
 

Author(s): Tiffany W Todd, Leonard Petrucelli

Journal: J. Neurochem.. 2016 Aug;138 Suppl 1():145-62.

 

The identification of a hexanucleotide repeat expansion in a non-coding region of C9orf72 as a major cause of both frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) drastically changed the field of research on both of these conditions. Yet, despite the vast amount ...

Last Updated: 31 Dec 1969

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Double jeopardy from a single translocation: deletions of the derivative chromosome 9 in chronic myeloid leukemia.
 

Author(s): Brian J P Huntly, Anthony Bench, Anthony R Green

Journal: Blood. 2003 Aug;102(4):1160-8.

 

Chronic myeloid leukemia (CML) is characterized by formation of a BCR-ABL fusion gene, usually as a consequence of the Philadelphia (Ph) translocation between chromosomes 9 and 22. Recently the development of new fluorescence in-situ hybridization (FISH) techniques has allowed identification ...

Last Updated: 31 Dec 1969

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Understanding Clinical Phenotype and Collecting Biomarker Samples in C9ORF72 ALS
 

Status: Recruiting

Condition Summary: C9ORF72 Amyotrophic Lateral Sclerosis (ALS)

 

Last Updated: 5 Jan 2017

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Nivolumab and Dasatinib in Treating Patients With Relapsed or Refractory Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia
 

Status: Recruiting

Condition Summary: B Acute Lymphoblastic Leukemia With t(9;22)(q34;q11.2); BCR-ABL1; Recurrent Adult Acute Lymphoblastic Leukemia; Recurrent Childhood Acute Lymphoblastic Leukemia; Refractory Adult Acute Lymphoblastic Leukemia; Refractory Childhood Acute Lymphoblastic Leukemia

 

Last Updated: 6 Sep 2017

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Imatinib Mesylate and Combination Chemotherapy in Treating Patients With Newly Diagnosed Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia
 

Status: Recruiting

Condition Summary: Acute Lymphoblastic Leukemia; B Acute Lymphoblastic Leukemia With t(9;22)(q34.1;q11.2); BCR-ABL1; BCR-ABL1 Fusion Protein Expression; Minimal Residual Disease; Philadelphia Chromosome Positive; T Acute Lymphoblastic Leukemia; Untreated Adult Acute Lymphoblastic Leukemia; Untreated Childhood Acute Lymphoblastic Leukemia

 

Last Updated: 6 Sep 2017

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