Works matching IS 00221333 AND DT 2023 AND VI 102 AND IP 1

Results: 30

CRISPR-Cas9 F0 knockout approach using predesigned in vitro transcribed guide RNAs partially recapitulates Rx3 function in eye morphogenesis.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01408-4

By:

Wysocka, Emilia;
Gonicka, Agata;
Anbalagan, Savani

Publication type:

Article

Dual effect of methylene-tetrahydrofolate reductase and angiotensin-converting enzyme gene polymorphisms on the risk of acute ischemic stroke.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01425-x

By:

Karakus, Nevin;
Yigit, Serbulent;
Basol, Nursah;
Incealtin, Onur

Publication type:

Article

EMX2OS targeting IGF2BP1 represses Wilms' tumour stemness, epithelial–mesenchymal transition and metastasis.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01411-9

By:

Zhang, Hong-Mei;
Cui, Ming-Yu;
Chen, Zhi-Hong

Publication type:

Article

Is the fundamental pathology in Duchenne's muscular dystrophy caused by a failure of glycogenolysis–glycolysis in costameres?

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01410-w

By:

Nesari, Vishakha;
Balakrishnan, Suresh;
Nongthomba, Upendra

Publication type:

Article

Exome sequencing and microarray identified a novel large exonic deletion in SYT2 gene in an ultra-rare case with recessive CMS type 7.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01409-3

By:

Kumar, C. P. Ravi;
Tamhankar, Parag M.;
Manohar, Radhika;
Sharda, Sheetal;
Madhavilatha, G. K.;
Thenral, S. G.;
Nair, Sandhya;
Bojamma, A. K.

Publication type:

Article

Prevalence of congenital sucrase-isomaltase deficiency in Turkey may be much higher than the estimates.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01428-8

By:

Taskin, Didem Gulcu;
Civan, Hasret Ayyildiz;
SarI, Emine Ergül;
Altuntaş, Cansu;
Ersoy, Melike;
Tuncel, Tolga;
Onay, Hüseyin;
Selimoğlu, Ayşe

Publication type:

Article

Role of cryptic rearrangements of human chromosomes in the aetiology of schizophrenia.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01427-9

By:

Jurisova, Livia;
Solc, Roman

Publication type:

Article

Identification of fertility restorers for A<sub>2</sub> cytoplasm-based CGMS lines and development of short duration hybrids in pigeonpea (Cajanus cajan (L.) Millsp.)

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01426-w

By:

Ranjani, M. S.;
Jayamani, P.

Publication type:

Article

Association of ABCA1 R219K polymorphism and telomere length in a Chinese rural population: possible linking to systemic inflammation.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01424-y

By:

Liao, Shutan;
Zhou, Qing;
Zhang, Yang

Publication type:

Article

Distinct gene expression patterns of SOX2 and SOX2OT variants in different types of brain tumours.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01423-z

By:

Fouani, Youssef;
Gholipour, Akram;
Oveisee, Maziar;
Shahryari, Alireza;
Saberi, Hooshang;
Mowla, Seyed Javad;
Malakootian, Mahshid

Publication type:

Article

Population genetic structure and evolutionary demographic patterns of Phrynoderma karaavali, an edible frog species of Kerala, India.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01407-5

By:

Anoop, V. S.;
George, Sanil

Publication type:

Article

Mitochondrial markers differentiate two distinct phylogenetic groups in indigenous rice landraces of northeast India: an evolutionary insight.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01422-0

By:

Parida, Madhuchhanda;
Gouda, Gayatri;
Chidambaranathan, Parameswaran;
Umakanta, Ngangkham;
Katara, Jawahar Lal;
Sai, Cayalvizhi Balasubramania;
Samantaray, Sanghamitra;
Patra, Bhaskar Chandra;
Mohapatra, Trilochan

Publication type:

Article

Differential expression of the androgen receptor gene is correlated with CAG polymorphic repeats in patients with prostate cancer.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01421-1

By:

Irigoyen Arredondo, Martín;
Romero Quintana, José;
Arámbula Meraz, Eliakym;
Bergez Hernández, Fernando;
Luque Ortega, Fred;
Martínez Camberos, Alejandra;
Álvarez Arrazola, Marco;
Romo Martínez, Enrique;
Cedano Prieto, Dora;
Contreras Gutiérrez, José;
García Magallanes, Noemi

Publication type:

Article

Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01420-2

By:

Mohammadi, Sanaz;
Jafari Khamirani, Hossein;
Zoghi, Sina;
Dastgheib, Seyed Alireza;
Tabei, Seyed Mohammad Bagher;
Talebzadeh, Mahdieh;
Adibi, Mohammad Hossein;
Dianatpour, Mehdi

Publication type:

Article

Transcribed intergenic regions exhibit a lower frequency of nucleotide polymorphism than the untranscribed intergenic regions in the genomes of Escherichia coli and Salmonella enterica.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01418-w

By:

Beura, Pratyush Kumar;
Sen, Piyali;
Aziz, Ruksana;
Satapathy, Siddhartha Shankar;
Ray, Suvendra Kumar

Publication type:

Article

Identification of genetic polymorphism of the MBL2 gene and its association with clinical mastitis in Murrah buffaloes.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01419-9

By:

Shergojry, Shahid Ahmad;
Verma, Archana;
Ghani, Minerva;
Gupta, Ishwar Dayal;
Mir, Nazir Ahmad

Publication type:

Article

First detection of endopolyploidy in tapetal cells and chromosomal anomalies in meiocytes of Viola pilosa cytotypes (2n=20) from Pir Panjal (Himalayas)

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01415-5

By:

Iqbal, Tasir;
Sharma, Geeta

Publication type:

Article

Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01417-3

By:

Jabbarpour, Neda;
Poorshiri, Bita;
Saei, Hassan;
Barzegar, Mohammad;
Bonyadi, Mortaza

Publication type:

Article

Individuals with T-786C and G894T genotypes of eNOS in Chinese Han population have an increased risk of developing rheumatoid arthritis.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01400-y

By:

LIN, SHAOPENG;
LIN, DAOQIANG;
QIU, LINAN;
WU, YUEPING;
LIU, XIN

Publication type:

Article

Imputation of SNPs associated with presbycusis through linkage disequilibrium analysis in the ILDR1 gene.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01416-4

By:

Flores, Sergio V.;
Levi-Monsalve, Alejandro;
Álvarez-Lobo, Juan Pablo

Publication type:

Article

Celiac disease-associated loci show considerable genetic overlap with neuropsychiatric diseases but with limited transethnic applicability.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01413-7

By:

Sharma, Nidhi;
Banerjee, Pratibha;
Sood, Ajit;
Midha, Vandana;
Thelma, B. K.;
Senapati, Sabyasachi

Publication type:

Article

A novel variant of TNNC1 associated with severe dilated cardiomyopathy causing infant mortality and stillbirth: a case of germline mosaicism.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01412-8

By:

Udani, Rupa;
Schilter, Kala F.;
Tyler, Rebecca C.;
Smith, Brandon A.;
Wendt-Andrae, Jaime L.;
Kappes, Ulrike P.;
Scharer, Gunter;
Lehman, Anna;
Steinraths, Michelle;
Reddi, Honey V.

Publication type:

Article

Diagnosis of prenatal 22q11.2 duplication syndrome: a two-case study.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01406-6

By:

Li, Hening;
Gong, Yanfei;
Chen, Jingyi;
Xie, Liyun;
Li, Bojie;
Xiang, Yanghai;
Xie, Meihua

Publication type:

Article

A time-calibrated mitogenomic phylogeny suggests that Korean Hyalessa fuscata is a bridge between Chinese and Japanese H. maculaticollis.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01405-7

By:

Nguyen, Hoa Quynh;
Ho, Phuong-Thao;
Kong, Sungsik;
Bae, Yoonhyuk;
Pham, Thai Hong;
La, Huyen Thi;
Jang, Yikweon

Publication type:

Article

Relationship between leptin gene variants (–2548G>A and 19A>G) and obesity among north Indian Punjabi population.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01401-x

By:

Kaur, Harjit;
Bains, Veena;
Sharma, Tanmayi;
Badaruddoza

Publication type:

Article

Remnants of SIRE1 retrotransposons in human genome?

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01398-3

By:

Guner, Buket Cakmak;
Karlik, Elif;
Gozukirmizi, Nermin

Publication type:

Article

LncRNA TTN-AS1 exacerbates extracellular matrix accumulation via miR-493-3p/FOXP2 axis in diabetic nephropathy.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01397-4

By:

Jia, Lin;
Wang, Wenzhe;
Liu, Hui;
Zhu, Fan;
Huang, Yunfang

Publication type:

Article

Panmictic stock structure of milkfish (Chanos chanos, Forsskål 1775) from Indian waters determined using mtDNA marker.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01395-6

By:

Jose, Divya Merin;
Divya, P. R.;
Lal, Kuldeep K.

Publication type:

Article

Arginase deficiency in Bulgaria: first cases and potential endemic region for the disorder.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01399-2

By:

Atemin, Slavena;
Todorov, Tihomir;
Tourtourikov, Ivan;
Ivanova, Mariya B.;
Chamova, Teodora;
Avdjieva-Tzavella, Daniela;
Kathom, Hadil;
Georgieva, Bilyana;
Guergueltcheva, Velina;
Bradinova, Irena;
Savov, Alexey;
Tournev, Ivailo;
Mitev, Vanyo;
Todorova, Albena

Publication type:

Article

Mysteries in our genome.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01392-9

By:

Kasbekar, Durgadas P.

Publication type:

Article