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    * Latest "Sequence-tagged-site-(STS)" in the News * 

 

 

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Novel Y-chromosomal microdeletions associated with non-obstructive azoospermia uncovered by high throughput sequencing of sequence-tagged sites (STSs)  Nature.com

Y-chromosomal microdeletion (YCM) serves as an important genetic factor in non-obstructive azoospermia (NOA). Multiplex polymerase chain reaction (PCR) is ...

Molecular mapping: Genetic and physical maps.  Science 2.0

Genome:A genome is all the DNA in anorganism, including its genes.• Comparative Sequence Sizes (Bases)• Escherichia coli(bacterium) genome 4.6 Million.

Copy number variation and microdeletions of the Y chromosome linked genes and loci across different categories of Indian infertile males  Nature.com

We analyzed 34 azoospermic (AZ), 43 oligospermic (OS), and 40 infertile males with normal spermiogram (INS) together with 55 normal fertile males (NFM) from ...

Defining and Evaluating a Core Genome Multilocus Sequence Typing Scheme for Genome-Wide Typing of Clostridium difficile  Journal of Clinical Microbiology

Clostridium difficile, recently renamed Clostridioides difficile, is the most common cause of antibiotic-associated nosocomial gastrointestinal infections worldwide ...

Whole-Genome Sequence Analysis of Streptococcus pneumoniae Strains That Cause Hospital-Acquired Pneumonia Infections  Journal of Clinical Microbiology

Streptococcus pneumoniae colonizes the nasopharyngeal mucus in healthy individuals and can cause otitis media, pneumonia, and invasive pneumococcal ...

Whole-Genome Sequencing of Recent Listeria monocytogenes Isolates from Germany Reveals Population Structure and Disease Clusters  Journal of Clinical Microbiology

Listeria monocytogenes causes foodborne outbreaks with high mortality. For improvement of outbreak cluster detection, the German consiliary laboratory for ...

HDAC Inhibitors Can Partially Reverse Genetic Signature Linked to FA, Study Shows  Friedreich's Ataxia News

Analysis shows that Friedreich's ataxia is linked to a genetic signature that can be partially reversed by HDAC inhibitors (HDACi).

Gene Therapy Approach in Early Tests Shows Potential to Raise Frataxin Protein Levels in Cells  Friedreich's Ataxia News

Read about a gene therapy approach that significantly increased frataxin protein production in cells of Friedreich's ataxia patients in preclinical tests.

Inhibition of FAST-1 Molecule May Have Therapeutic Potential in Friedreich’s Ataxia, Study Confirms  Friedreich's Ataxia News

A study supports the hypothesis that inhibition of FAST-1, a naturally produced RNA molecule, may have potential for the treatment of Friedreich's ataxia.

Ultrafast manipulation of mirror domain walls in a charge density wave  Science Advances

Domain walls (DWs) are singularities in an ordered medium that often host exotic phenomena such as charge ordering, insulator-metal transition, ...

Large Interruptions in GAA Repeats are Rare Among FA Patients, Study Finds  Friedreich's Ataxia News

Large interruptions of GAA repeats in the frataxin (FXN) gene are very rare among patients with Friedreich's ataxia (FA), a study has found. However, when these ...

Case Report Describes Early FA Onset in Boy with Rare Gene Mutation  Friedreich's Ataxia News

A new case report describes a 7-year-old boy with Friedreich's ataxia (FA) who has a particularly early age of disease onset and an extremely rare type of ...

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STS - Wikipedia
This disambiguation page lists articles associated with the title STS. If an internal link led you here, you may wish to change the link to point directly to the intended article.

STS — Wikipédia
Sigles de 2 caractères Sigles de 3 caractères Sigles de 4 caractères Sigles de 5 caractères Sigles de 6 caractères Sigles de 7 caractères Sigles de 8 caractères

Contig - Wikipedia
A contig (from contiguous) is a set of overlapping DNA segments that together represent a consensus region of DNA. In bottom-up sequencing projects, a contig refers to overlapping sequence data (reads); in top-down sequencing projects, contig refers to the overlapping clones that form a physical map of the genome that is used to guide sequencing and assembly.

NCBI BLAST < Sequence Similarity Searching < EMBL-EBI
BLAST stands for Basic Local Alignment Search Tool.The emphasis of this tool is to find regions of sequence similarity, which will yield functional and evolutionary clues about the structure and function of your sequence.

OMIM Entry - * 601513 - FIBROBLAST GROWTH FACTOR 12; FGF12
By Southern blot hybridization of genomic DNA from rodent/human hybrid cell lines containing individual human chromosomes, Smallwood et al. (1996) demonstrated that the human FHF1 (also symbolized FGF12), FHF2 (), FHF3 (), and FHF4 genes are located on chromosomes 3, X, 17, and 13, respectively.They found that a sequence tagged site (STS) that encompassed 1 exon of FHF3 was derived from human ...

유전학 용어 정리 [펌] : 네이버 블로그
G bands(G 밴드): 염색체 분석시 트립신 처리후 김자(Giemsa)로 염색하여 나타나는 염색체상의 명.암의 교차 띠. gamete(배우자): 반수체의 염색체수를 가진 웅성 생식세포인 정자나 자성 생식 세포인 난자. gene map(유전자지도): 자신의 위치를 지도위에서 표현하듯, 유전자의 염색체 상의 위치를 나타낸 ...

Biology Dictionary - S - Macroevolution.net
sarcoma /sar-KŌM-ə/ n. Cancer of muscle or connective tissue.Specific types of sarcomas are named for the types of tissue from which they arise (e.g., angiosarcoma, chondrosarcoma, hemangiosarcoma, leiomyosarcoma, liposarcoma, lymphangiosarcoma, osteosarcoma, rhabdomyosarcoma). sarcomere /SARK-ə-meer/ n. The sarcomere is the fundamental unit of muscle structure.

OMIM Entry - * 114240 - CALPAIN 3; CAPN3
The CAPN3 gene encodes calpain-3. The calpains, or calcium-activated neutral proteases (EC 3.4.22.17), are nonlysosomal intracellular cysteine proteases.Mammalian calpains are heterodimers composed of a ubiquitous 80-kD large subunit (e.g., CAPN1, 114220 and CAPN2, 114230) and a common small 30-kD subunit (CAPNS1; 114170).CAPN3 is a muscle-specific large subunit (Sorimachi et al., 1989).

GLOSSARY OF MEDICAL AND MOLECULAR GENETICS
This French / English glossary of medical and molecular genetics is intended for students in human and biological sciences as well as medical and para-medical personnel.

The DDBJ/ENA/GenBank Feature Table Definition | INSDC
The DDBJ/ENA/GenBank Feature Table: Definition Version 10.8 December 2018 DNA Data Bank of Japan, Mishima, Japan. EMBL-EBI, European Nucleotide Archive, Cambridge, UK.


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