United States News Beep
  • News Beep
  • Breaking News
  • Business
  • Entertainment
  • Health
  • Science
  • Sports
  • Technology
United States News Beep
United States News Beep
  • News Beep
  • Breaking News
  • Business
  • Entertainment
  • Health
  • Science
  • Sports
  • Technology

Browsing Tag

Human Genetics

46 posts
GGenetics
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)
Read More

Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)

  • September 6, 2025
Capone VP, Morello W, Taroni F, Montini G. Genetics of congenital anomalies of the kidney and urinary tract:…
GGenetics
Improving broad-spectrum resistance to clubroot disease with one gene
Read More

Improving broad-spectrum resistance to clubroot disease with one gene

  • September 5, 2025
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. This…
GGenetics
A multi-tissue single-cell expression atlas in cattle
Read More

A multi-tissue single-cell expression atlas in cattle

  • September 5, 2025
The scope of CattleCA After removing low-quality cells and doublets (Methods, Supplementary Fig. 1 and Supplementary Tables 1…
GGenetics
Molecular genetics and therapeutic development for GNE myopathy
Read More

Molecular genetics and therapeutic development for GNE myopathy

  • September 5, 2025
Yoshioka W, Noguchi S, Mori-Yoshimura M, Nishino I. Advances in understanding of the natural history, mechanism, extra-muscular manifestations…
GGenetics
DNA methylation influences human centromere positioning and function
Read More

DNA methylation influences human centromere positioning and function

  • September 4, 2025
This study complied with all relevant local ethical regulations. Approval for the use of ICF patients’ fibroblasts was…
GGenetics
A novel MCMDC2 variant causes meiotic arrest and non-obstructive azoospermia in a consanguineous Chinese family
Read More

A novel MCMDC2 variant causes meiotic arrest and non-obstructive azoospermia in a consanguineous Chinese family

  • September 2, 2025
Cerván-Martín M, Castilla JA, Palomino-Morales RJ, Carmona FD. Genetic landscape of nonobstructive azoospermia and new perspectives for the…
GGenetics
Chromatin dynamics of a large-sized genome provides insights into polyphenism and X0 dosage compensation of locusts
Read More

Chromatin dynamics of a large-sized genome provides insights into polyphenism and X0 dosage compensation of locusts

  • September 1, 2025
Chromosome-level assembly of the migratory locust We conducted genome sequencing on an adult female locust with a heterozygosity…
GGenetics
MYH2-associated myopathy caused by novel compound heterozygous mutations: a case report and literature review
Read More

MYH2-associated myopathy caused by novel compound heterozygous mutations: a case report and literature review

  • September 1, 2025
Morales PN, Coons AN, Koopman AJ, Patel S, Chase PB, Parvatiyar MS, et al. Post-translational modifications of vertebrate…
GGenetics
Epidemiological report and diagnostic approach used in the neuromuscular population of Liege, Belgium | Orphanet Journal of Rare Diseases
Read More

Epidemiological report and diagnostic approach used in the neuromuscular population of Liege, Belgium | Orphanet Journal of Rare Diseases

  • August 29, 2025
Laing NG. Genetics of neuromuscular disorders. Crit Rev Clin Lab Sci. 2012;49:33–48. CAS  PubMed  Google Scholar  Carey IM,…
GGenetics
Cross-biobank generalizability and accuracy of electronic health record-based predictors compared to polygenic scores
Read More

Cross-biobank generalizability and accuracy of electronic health record-based predictors compared to polygenic scores

  • August 27, 2025
Ethics declarations Patients and control participants in FinnGen provided informed consent for biobank research, based on the Finnish…
GGenetics
Clinical features and genetic analysis of A20 haploinsufficiency | Orphanet Journal of Rare Diseases
Read More

Clinical features and genetic analysis of A20 haploinsufficiency | Orphanet Journal of Rare Diseases

  • August 26, 2025
The A20 acts as a critical negative regulator of the NF-κB signaling pathway by suppressing inflammatory cascades through…
GGenetics
Precise modulation of BRG1 levels reveals features of mSWI/SNF dosage sensitivity
Read More

Precise modulation of BRG1 levels reveals features of mSWI/SNF dosage sensitivity

  • August 22, 2025
BRG1 binding exhibits a linear response to its dosage In mES cells, Brg1 encodes the major catalytic subunit…
United States News Beep
www.newsbeep.com