Results 151 to 160 of about 10,211 (221)

A Review of Contributing Factors to Heart Failure: Genetic, Lifestyle, and Environmental Influences. [PDF]

J Pharm Bioallied Sci
Thotakura B, Vidya S, Sheena KS, Roy DD, Prabhu K, Jones S.   +5 more
europepmc   +1 more source

Study of the meiotic segregation of chromosome 7 with a paracentric inversion in spermatosoa of a heterozygous carrier. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Antonova MM, Yurchenko DA, Markova ZG, Shilova NV.   +3 more
europepmc   +1 more source

A genomic resource for medicinal plant research: chloroplast genome assembly and annotation of <i>Helicteres isora</i> L. [PDF]

Front Plant Sci
Sudarmono S, Nugroho A, Damayanti RU, Sudomo A, Lailaty IQ, Diantina S, Nugraheni YMMA, Palupi KD, Prameswari D.   +8 more
europepmc   +1 more source

Preliminary study of genetic variation in the CYP26B1 gene coding region in Bali cattle bulls. [PDF]

Open Vet J
Mulyati N, Noor RR, Jakaria J.
europepmc   +1 more source

Prokaryotic communities profiling of Indonesian hot springs using long-read Oxford Nanopore sequencing. [PDF]

BMC Res Notes
Wirajana IN, Ariantari NP, Shyu DJH, Vaghamshi N, Antaliya K, Dudhagara P.   +5 more
europepmc   +1 more source

Genetika frontotemporalnih demencija

Frontotemporalna demencija (FTD) je progresivni neurodegenerativni poremećaj koji prvenstveno zahvaća frontalne i temporalne režnjeve mozga dovodeći do značajnih promjena u osobnosti, ponašanju i govoru. To je drugi najčešći uzrok demencije s ranim početkom koji tipično pogađa osobe između 45. i 65. godine života. Etiologija FTD-a je vrlo heterogena, a
openaire   +1 more source

Familial translocation between chromosomes 3 and 10: meiotic segregation, diagnostics and clinical features of chromosomal imbalance. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Vozilova AV, Tarasova AS, Ivanov EA, Pushkarev VP, Nalyotova NI, Pobedinskaya AI, Sabitova AS, Shilova NV.   +7 more
europepmc   +1 more source

Selecting stable rice mutants with linear mixed models (LMM) and stability indexes. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Sharifi P, Ebadi AA, Hallajian MT, Aminpanah H.   +3 more
europepmc   +1 more source

Heparan sulfate in cerebrospinal fluid as a biomarker to assess disease severity and for treatment monitoring in patients with Mucopolysaccharidosis Type II: a position statement. [PDF]

Orphanet J Rare Dis
Giugliani R, de Siqueira ACM, Santos ES, Leão EKEA, Carvalho GDS, Santos MLSF, Raskin S, Martins AM.   +7 more
europepmc   +1 more source

Genetika retinitis pigmentose

Retinitis pigmentosa (RP) is a group of inherited retinal dystrophies characterized by progressive degeneration of photoreceptors, primarily rods and later cones. The disease typically presents with night blindness, narrowing of the visual field, and in advanced stages, severe vision loss.
openaire   +1 more source