Kinetic signatures of myosin-5B, the motor involved in microvillus inclusion disease.
The Journal of biological chemistry | 2017-11-03 | PMID 28882893
Heissler Sarah M, Chinthalapudi Krishna, Sellers James R
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 7482 of 10600
Transcriptional fidelities of human mitochondrial POLRMT, yeast mitochondrial Rpo41, and phage T7 single-subunit RNA polymerases.
The Journal of biological chemistry | 2017-11-03 | PMID 28882896
Sultana Shemaila, Solotchi Mihai, Ramachandran Aparna and 1 more
Genes: POLRMT, TEFM
Glucose-Induced Changes in Gene Expression in Human Pancreatic Islets: Causes or Consequences of Chronic Hyperglycemia.
Diabetes | 2017-12-01 | PMID 28882899
Ottosson-Laakso Emilia, Krus Ulrika, Storm Petter and 7 more
Genes: DOCK10, IGSF11
Predictors of HIV virological failure and drug resistance in Chinese patients after 48 months of antiretroviral treatment, 2008-2012: a prospective cohort study.
BMJ open | 2017-09-07 | PMID 28882911
Kan Wei, Teng Tao, Liang Shujia and 13 more
Phe354Leu Polymorphism of LKB1 Is a Potential Prognostic Factor for Cytogenetically Normal Acute Myeloid Leukemia.
In vivo (Athens, Greece) | 2000-01-01 | PMID 28882949
Yang Ming-Yu, Hsiao Hui-Hua, Liu Yi-Chang and 3 more
Genes: FLT3, IDH1, IDH2, NPM1
SCARB1 Gene Polymorphisms and HDL Subfractions in Coronary Artery Disease.
In vivo (Athens, Greece) | 2000-01-01 | PMID 28882953
Ayhan Huseyin, Gormus Uzay, Isbir Selim and 2 more
Genes: SCARB1, CAD
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH).
European journal of endocrinology | 2018-01-01 | PMID 28882981
Bonomi Marco, Vezzoli Valeria, Krausz Csilla and 27 more
Genes: IHH
Laparoscopic adrenalectomy as an effective approach to massive bilateral pheochromocytomas.
BMJ case reports | 2017-09-07 | PMID 28883010
Martins Diana, Rodrigues Dírcea, Melo Miguel and 1 more
Genes: RET
NFκB signaling in alveolar rhabdomyosarcoma.
Disease models & mechanisms | 2017-09-01 | PMID 28883017
Cleary Megan M, Mansoor Atiya, Settelmeyer Teagan and 6 more
Human leukocyte antigen-E mismatch is associated with better hematopoietic stem cell transplantation outcome in acute leukemia patients.
Haematologica | 2017-11-01 | PMID 28883078
Tsamadou Chrysanthi, Fürst Daniel, Vucinic Vladan and 10 more
Genes: NRM
Phenotype in combination with genotype improves outcome prediction in acute myeloid leukemia: a report from Children's Oncology Group protocol AAML0531.
Haematologica | 2017-12-01 | PMID 28883080
Voigt Andrew P, Brodersen Lisa Eidenschink, Alonzo Todd A and 10 more
Integrin α8 and Pcdh15 act as a complex to regulate cilia biogenesis in sensory cells.
Journal of cell science | 2017-11-01 | PMID 28883094
Goodman Linda, Zallocchi Marisa
COG7 deficiency in Drosophila generates multifaceted developmental, behavioral and protein glycosylation phenotypes.
Journal of cell science | 2017-11-01 | PMID 28883096
Frappaolo Anna, Sechi Stefano, Kumagai Tadahiro and 8 more
Genes: COG7, COG1, COG2, COG4, COG8
Standards-Based Procedural Phenotyping: The Arden Syntax on i2b2.
Studies in health technology and informatics | 2017-01-01 | PMID 28883166
Mate Sebastian, Castellanos Ixchel, Ganslandt Thomas and 2 more
Acute myeloid leukemia in adolescents and young adults: from the viewpoint of physicians.
[Rinsho ketsueki] The Japanese journal of clinical hematology | 2017-01-01 | PMID 28883268
Kuwatsuka Yachiyo
Pediatric acute myeloid leukemia with genetic alterations.
[Rinsho ketsueki] The Japanese journal of clinical hematology | 2017-01-01 | PMID 28883284
Shimada Akira
Genes: FLT3, KIT
Genetic abnormalities in core binding factor acute myeloid leukemia.
[Rinsho ketsueki] The Japanese journal of clinical hematology | 2017-01-01 | PMID 28883285
Ishikawa Yuichi
Genes: CBFB, MYH11, RUNX1, ASXL2, CCND2, DHX15, FLT3, KIT
Computational genome-wide survey of odorant receptors from two solitary bees Dufourea novaeangliae (Hymenoptera: Halictidae) and Habropoda laboriosa (Hymenoptera: Apidae).
Scientific reports | 2017-09-07 | PMID 28883425
Karpe Snehal D, Dhingra Surbhi, Brockmann Axel and 1 more
Assessing SNP genotyping of noninvasively collected wildlife samples using microfluidic arrays.
Scientific reports | 2017-09-07 | PMID 28883428
von Thaden Alina, Cocchiararo Berardino, Jarausch Anne and 5 more
A massive tsunami promoted gene flow and increased genetic diversity in a near threatened plant species.
Scientific reports | 2017-09-07 | PMID 28883435
Ohbayashi Kako, Hodoki Yoshikuni, I Kondo Natsuko and 2 more
Mechanism and DNA-based detection of field-evolved resistance to transgenic Bt corn in fall armyworm (Spodoptera frugiperda).
Scientific reports | 2017-09-07 | PMID 28883440
Banerjee Rahul, Hasler James, Meagher Robert and 5 more
Genes: ABCC2
QTL mapping using an ultra-high-density SNP map reveals a major locus for grain yield in an elite rice restorer R998.
Scientific reports | 2017-09-07 | PMID 28883457
Zhu Manshan, Liu Dilin, Liu Wuge and 9 more
Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood.
Nature communications | 2017-09-07 | PMID 28883458
Lukowski Samuel W, Lloyd-Jones Luke R, Holloway Alexander and 15 more
Genome-wide identification and co-expression network analysis provide insights into the roles of auxin response factor gene family in chickpea.
Scientific reports | 2017-09-07 | PMID 28883480
Singh Vikash K, Rajkumar Mohan Singh, Garg Rohini and 1 more
Early X chromosome inactivation during human preimplantation development revealed by single-cell RNA-sequencing.
Scientific reports | 2017-09-07 | PMID 28883481
Moreira de Mello Joana C, Fernandes Gustavo R, Vibranovski Maria D and 1 more
SERPINB2 is a novel TGFβ-responsive lineage fate determinant of human bone marrow stromal cells.
Scientific reports | 2017-09-07 | PMID 28883483
Elsafadi Mona, Manikandan Muthurangan, Atteya Muhammad and 8 more
Genes: SERPINB2
FLO5 gene controls flocculation phenotype and adhesive properties in a Saccharomyces cerevisiae sparkling wine strain.
Scientific reports | 2017-09-07 | PMID 28883485
Di Gianvito Paola, Tesnière Catherine, Suzzi Giovanna and 2 more
Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors.
Nature communications | 2017-09-07 | PMID 28883545
Martin-Trujillo Alex, Vidal Enrique, Monteagudo-Sánchez Ana and 7 more
Adaptive mutations of neuraminidase stalk truncation and deglycosylation confer enhanced pathogenicity of influenza A viruses.
Scientific reports | 2017-09-07 | PMID 28883554
Park Sehee, Il Kim Jin, Lee Ilseob and 9 more
Genome-wide association study Identified multiple Genetic Loci on Chilling Resistance During Germination in Maize.
Scientific reports | 2017-09-07 | PMID 28883611
Hu Guanghui, Li Zhao, Lu Yuncai and 15 more
Development of new experimental platform 'MARS'-Multiple Artificial-gravity Research System-to elucidate the impacts of micro/partial gravity on mice.
Scientific reports | 2017-09-07 | PMID 28883615
Shiba Dai, Mizuno Hiroyasu, Yumoto Akane and 10 more
SOCS2 Binds to and Regulates EphA2 through Multiple Mechanisms.
Scientific reports | 2017-09-07 | PMID 28883622
Pilling Carissa, Cooper Jonathan A
Genes: SOCS2, SOCS6
Genomic epidemiology of a national outbreak of post-surgical Mycobacterium abscessus wound infections in Brazil.
Microbial genomics | 2017-05-01 | PMID 28884021
Everall Izzy, Nogueira Christiane Lourenço, Bryant Josephine M and 13 more
Genetic Association Study of KCNQ5 Polymorphisms with High Myopia.
BioMed research international | 2017-01-01 | PMID 28884119
Liao Xuan, Yap Maurice K H, Leung Kim Hung and 3 more
Genes: KCNQ5
Development of Brassica oleracea-nigra monosomic alien addition lines: genotypic, cytological and morphological analyses.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2017-12-01 | PMID 28884205
Tan Chen, Cui Cheng, Xiang Yi and 2 more
The Changing Presentation of Paget's Disease of Bone in Australia, A High Prevalence Region.
Calcified tissue international | 2017-12-01 | PMID 28884211
Britton Cameron, Brown Suzanne, Ward Lynley and 3 more
Genes: SQSTM1
MicroRNA expression changes following synthesis of three full-sib Populus triploid populations with different heterozygosities.
Plant molecular biology | 2017-10-01 | PMID 28884266
Suo Yujing, Min Yu, Dong Chunbo and 3 more
Dispersals of the Siberian Y-chromosome haplogroup Q in Eurasia.
Molecular genetics and genomics : MGG | 2018-02-01 | PMID 28884289
Huang Yun-Zhi, Pamjav Horolma, Flegontov Pavel and 9 more
Implications of fALS Mutations on Sod1 Function and Oligomerization in Cell Models.
Molecular neurobiology | 2018-06-01 | PMID 28884318
Brasil Aline A, Magalhães Rayne S S, De Carvalho Mariana D C and 5 more
Influenza-associated thrombotic microangiopathies.
Pediatric nephrology (Berlin, Germany) | 2018-11-01 | PMID 28884355
Bitzan Martin, Zieg Jakub
Genes: ADAMTS13, CFB
IDH mutation status trumps the Pignatti risk score as a prognostic marker in low-grade gliomas.
Journal of neuro-oncology | 2017-11-01 | PMID 28884377
Etxaniz Olatz, Carrato Cristina, de Aguirre Itziar and 12 more
Genes: MGMT
Genetic interaction of purinergic P2X7 receptor and ER-α polymorphisms in susceptibility to osteoporosis in Chinese postmenopausal women.
Journal of bone and mineral metabolism | 2018-07-01 | PMID 28884379
Wang Hui, Gong Chengxin, Liu Xingzi and 16 more
BRCA1 gene: function and deficiency.
International journal of clinical oncology | 2018-02-01 | PMID 28884397
Takaoka Miho, Miki Yoshio
Genes: BRCA1
Pharmacotherapy for smoking cessation: effects by subgroup defined by genetically informed biomarkers.
The Cochrane database of systematic reviews | 2017-09-08 | PMID 28884473
Schuit Ewoud, Panagiotou Orestis A, Munafò Marcus R and 3 more
Genes: CHRNA3, CHRNA5, DRD4, EGLN2
[Screening of different AFLP fragments between near-isogenic lines of male sterile and fertile Salvia miltiorrhiza and their comparison analysis].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica | 2016-04-01 | PMID 28884532
Liang Wen-Jie, Lu Cong-Yu, Shu Zhi-Ming and 5 more
The MtrAB two-component system controls antibiotic production in Streptomyces coelicolor A3(2).
Microbiology (Reading, England) | 2017-10-01 | PMID 28884676
Som Nicolle F, Heine Daniel, Holmes Neil and 6 more
[A search of target regions for association studies between DNA methylation and cognitive impairment in schizophrenia].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova | 2000-01-01 | PMID 28884721
Kondratiev N V, Alfimova M V, Golimbet V E
Genes: BDNF, COMT, PSMA4, RELN, SNRPN
Inflammatory leiomyosarcoma is a distinct tumor characterized by near-haploidization, few somatic mutations, and a primitive myogenic gene expression signature.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | 2018-01-01 | PMID 28884746
Arbajian Elsa, Köster Jan, Vult von Steyern Fredrik and 1 more
Genes: ITGA7, MYF5, MYF6, MYOD1, MYOG, PAX7
The composition of potentially bioactive triterpenoid glycosides in red raspberry is influenced by tissue, extraction procedure and genotype.
Food & function | 2017-10-18 | PMID 28884768
McDougall Gordon J, Allwood J William, Pereira-Caro Gema and 10 more
Fitness change in relation to mutation number in spontaneous mutation accumulation lines of Chlamydomonas reinhardtii.
Evolution; international journal of organic evolution | 2017-12-01 | PMID 28884790
Kraemer Susanne A, Böndel Katharina B, Ness Robert W and 2 more
How does mutation affect the distribution of phenotypes?
Evolution; international journal of organic evolution | 2017-10-01 | PMID 28884791
McGuigan Katrina, Aw Ernest
Pathology Evaluation of Developmental Phenotypes in Neonatal and Juvenile Mice.
Current protocols in mouse biology | 2017-09-08 | PMID 28884794
Bolon Brad, Newbigging Susan, Boyd Kelli L
Assortment and the analysis of natural selection on social traits.
Evolution; international journal of organic evolution | 2017-11-01 | PMID 28884795
McDonald Grant C, Farine Damien R, Foster Kevin R and 1 more
Insights into the genetic structure of the rabbitfish Chimaera monstrosa (Holocephali) across the Atlantic-Mediterranean transition zone.
Journal of fish biology | 2017-10-01 | PMID 28884814
Catarino D, Stanković D, Menezes G and 1 more
Association Between CYP2C19*17 Alleles and pH Probe Testing Outcomes in Children With Symptomatic Gastroesophageal Reflux.
Journal of clinical pharmacology | 2018-01-01 | PMID 28884817
Franciosi James P, Mougey Edward B, Williams Andre and 6 more
Overexpression of miR-216b: Prognostic and predictive value in acute myeloid leukemia.
Journal of cellular physiology | 2018-04-01 | PMID 28884855
Zhang Ting-Juan, Wu De-Hong, Zhou Jing-Dong and 7 more
Genes: FLT3, IDH1
A novel missense variant in the GLI3 zinc finger domain in a family with digital anomalies.
American journal of medical genetics. Part A | 2017-12-01 | PMID 28884880
Crapster J Aaron, Hudgins Louanne, Chen James K and 1 more
Genes: GLI3
FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
American journal of medical genetics. Part A | 2017-12-01 | PMID 28884888
Myers Angela, du Souich Christèle, Yang Connie L and 6 more
Genes: FOXP1
Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45.
American journal of medical genetics. Part A | 2017-11-01 | PMID 28884889
Straussberg Rachel, Onoufriadis Alexandros, Konen Osnat and 6 more
Chimerism for 20q11.2 microdeletion of GDF5 explains discordant phenotypes in monochorionic-diamniotic twins.
American journal of medical genetics. Part A | 2017-12-01 | PMID 28884893
Meredith Matthew M, Crabb Beau, Vargas Marcelo and 1 more
Genes: GDF5
Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations.
Pediatric dermatology | 2017-09-01 | PMID 28884918
Jones Krystal M, Silfvast-Kaiser Annika, Leake David R and 2 more
Genes: DOCK6
Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1.
American journal of medical genetics. Part A | 2017-11-01 | PMID 28884921
Said Edith, Chong Jessica X, Hempel Maja and 7 more
Genes: GLE1
Two novel mutations in XYLT2 cause spondyloocular syndrome.
American journal of medical genetics. Part A | 2017-12-01 | PMID 28884924
Taylan Fulya, Yavaş Abalı Zehra, Jäntti Nina and 7 more
Genes: XYLT2
Variable phenotypic expression in a large Noonan syndrome family segregating a novel SOS1 mutation.
American journal of medical genetics. Part A | 2017-11-01 | PMID 28884940
van Trier Dorothée C, Rinne Tuula, Noordam Kees and 2 more
Genes: SOS1
Characterization of the novel HLA-DQB1*05:155 allele by sequencing-based typing.
HLA | 2017-12-01 | PMID 28884941
Zhang L-Q, Zhou X-Y, Xiao Y and 1 more
Characterization of the novel HLA-A*02:07:10 allele by sequencing-based typing.
HLA | 2017-12-01 | PMID 28884944
Zhang L-Q, Zhou X-Y, Xiao Y and 1 more
Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability.
American journal of medical genetics. Part A | 2017-11-01 | PMID 28884947
Van Paemel Ruben, De Bruyne Pauline, van der Straaten Saskia and 5 more
Genes: ARID2
HLA-B*40:302, a novel allele identified by sequence-based typing in a Korean individual.
HLA | 2017-12-01 | PMID 28884955
Lee J H, Im J, Choi H-J and 2 more
Identification of HLA-B*58:01:21, a novel allele in a Korean individual.
HLA | 2017-12-01 | PMID 28884963
Lee J H, Choi H-J, Kim S-H and 1 more
Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial clefting.
American journal of medical genetics. Part A | 2017-11-01 | PMID 28884971
Roosenboom Jasmien, Indencleef Karlijne, Hens Greet and 6 more
A novel multiplex polymerase chain reaction assay for detection of both HLA-A*31:01/HLA-B*15:02 alleles, which confer susceptibility to carbamazepine-induced severe cutaneous adverse reactions.
HLA | 2017-12-01 | PMID 28884973
Nguyen D V, Vidal C, Chi H C and 4 more
Genes: SSB
New therapeutic approach by sirolimus for enteropathy treatment in patients with LRBA deficiency.
European annals of allergy and clinical immunology | 2017-09-01 | PMID 28884992
Azizi G, Abolhassani H, Yazdani R and 5 more
Genes: LRBA
Next-Generation Sequencing Promoted the Release of Reference Genomes and Discovered Genome Evolution in Cereal Crops.
Current issues in molecular biology | 2018-01-01 | PMID 28885173
Huang Yong, Liu Haiyang, Xing Yongzhong
Advanced Applications of Next-Generation Sequencing Technologies to Orchid Biology.
Current issues in molecular biology | 2018-01-01 | PMID 28885174
Yeh Chuan-Ming, Liu Zhong-Jian, Tsai Wen-Chieh
A Rice Genetic Improvement Boom by Next Generation Sequencing.
Current issues in molecular biology | 2018-01-01 | PMID 28885178
Zhou Xiangchun, Bai Xufeng, Xing Yongzhong
Cataloging Plant Genome Structural Variations.
Current issues in molecular biology | 2018-01-01 | PMID 28885182
Zhang Xingtan, Chen Xuequn, Liang Pingping and 1 more
Genetic and Transcriptomic Bases of Intestinal Epithelial Barrier Dysfunction in Inflammatory Bowel Disease.
Inflammatory bowel diseases | 2017-10-01 | PMID 28885228
Vancamelbeke Maaike, Vanuytsel Tim, Farré Ricard and 8 more
Genes: MUC1, MUC4, PTGER4
Epigenetic Alterations in Bone and Soft Tissue Tumors.
Advances in anatomic pathology | 2017-11-01 | PMID 28885261
Wojcik John, Cooper Kumarasen
PIK3CG single nucleotide polymorphisms are associated with poor responsiveness to clopidogrel and increased risk of ischemia in patients with coronary heart disease.
Medicine | 2017-09-01 | PMID 28885323
Li Ke-Cheng, Yu Shu-Hong, Zhuge Bao-Zhong
B-cell lymphocyte kinase polymorphisms rs13277113, rs2736340, and rs4840568 and risk of autoimmune diseases: A meta-analysis.
Medicine | 2017-09-01 | PMID 28885337
Zeng Chang, Fang Cheng, Weng Hong and 3 more
Genes: BLK
Association between MDM2 SNP309, p53 Arg72Pro, and hepatocellular carcinoma risk: A MOOSE-compliant meta-analysis.
Medicine | 2017-09-01 | PMID 28885338
Duan Xiaohua, Li Jingquan
Genes: MDM2
Structure of Pigment Metabolic Pathways and Their Contributions to White Tepal Color Formation of Chinese Narcissus tazetta var. chinensis cv Jinzhanyintai.
International journal of molecular sciences | 2017-09-08 | PMID 28885552
Ren Yujun, Yang Jingwen, Lu Bingguo and 5 more
Re-Assembly and Analysis of an Ancient Variola Virus Genome.
Viruses | 2017-09-08 | PMID 28885569
Smithson Chad, Imbery Jacob, Upton Chris
Anti-HIV Activities and Mechanism of 12-O-Tricosanoylphorbol-20-acetate, a Novel Phorbol Ester from Ostodes katharinae.
Molecules (Basel, Switzerland) | 2017-09-08 | PMID 28885587
Chen Huan, Zhang Rong, Luo Rong-Hua and 4 more
Hypoxia Is a Critical Parameter for Chondrogenic Differentiation of Human Umbilical Cord Blood Mesenchymal Stem Cells in Type I/III Collagen Sponges.
International journal of molecular sciences | 2017-09-08 | PMID 28885597
Gómez-Leduc Tangni, Desancé Mélanie, Hervieu Magalie and 6 more
Genes: MMP13, MSC, UBC
Crystal structure of E. coli apolipoprotein N-acyl transferase.
Nature communications | 2017-07-04 | PMID 28885614
Lu Guangyuan, Xu Yingzhi, Zhang Kai and 8 more
Necroptosis in microglia contributes to neuroinflammation and retinal degeneration through TLR4 activation.
Cell death and differentiation | 2018-01-01 | PMID 28885615
Huang Zijing, Zhou Tian, Sun Xiaowei and 5 more
Genes: TLR4
Circulating tumor DNA is effective for detection of KRAS mutation in colorectal cancer: a meta-analysis.
The International journal of biological markers | 2017-10-31 | PMID 28885658
Tang Min, Deng Zhenghua, Li Baolin and 3 more
Genes: KRAS
EGFR as a clinical marker in glioblastomas and other gliomas.
The International journal of biological markers | 2018-01-01 | PMID 28885661
Saadeh Fadi S, Mahfouz Rami, Assi Hazem I
Genes: EGFR
Novel ABCA4 mutation leads to loss of a conserved C-terminal motif: implications for predicting pathogenicity based on genetic testing.
European journal of ophthalmology | 2018-01-01 | PMID 28885670
Wangtiraumnuay Nutsuchar, Capasso Jenina, Tsukikawa Mai and 2 more
Genes: ABCA4
Epidemiological and molecular analysis of hepatitis B virus infection in manicurists in Central Brazil.
Journal of medical virology | 2018-02-01 | PMID 28885693
Cavaretto Larissa, Motta-Castro Ana R C, Teles Sheila A and 10 more
Hepatitis B among immigrants from Myanmar: Genotypes and their clinical relevance.
Journal of medical virology | 2018-02-01 | PMID 28885711
Schulz Thomas R, Edwards Rosalind, Thurnheer M Christine and 8 more
Chronic myelomonocytic leukemia masquerading as cutaneous indeterminate dendritic cell tumor: Expanding the spectrum of skin lesions in chronic myelomonocytic leukemia.
Journal of cutaneous pathology | 2017-12-01 | PMID 28885734
Loghavi Sanam, Curry Jonathan L, Garcia-Manero Guillermo and 15 more
Genes: KRAS
Characterization of the novel HLA-DRB1*13:241 allele by sequencing-based typing.
HLA | 2017-12-01 | PMID 28885768
Zhang L-Q, Zhou X-Y, Xiao Y and 1 more
Monitoring of transferrin isoforms in biological samples by capillary electrophoresis.
Journal of separation science | 2018-01-01 | PMID 28885776
Caslavska Jitka, Thormann Wolfgang
Changes in Tonsil B Cell Phenotypes and EBV Receptor Expression in Children Under 5-Years-Old.
Cytometry. Part B, Clinical cytometry | 2018-03-01 | PMID 28885784
Wohlford Eric M, Baresel Paul C, Wilmore Joel R and 3 more
Attachment Site Cysteine Thiol pKa Is a Key Driver for Site-Dependent Stability of THIOMAB Antibody-Drug Conjugates.
Bioconjugate chemistry | 2017-10-18 | PMID 28885827
Vollmar Breanna S, Wei Binqing, Ohri Rachana and 15 more
Clinical characteristics of recessive retinal degeneration due to mutations in the CDHR1 gene and a review of the literature.
Ophthalmic genetics | 2000-01-01 | PMID 28885867
Bessette A P, DeBenedictis M J, Traboulsi E I
Genes: CDHR1
A Genetic Variant of ASCT2 Hampers In Vitro RNA Splicing and Correlates with Human Longevity.
Rejuvenation research | 2018-06-01 | PMID 28885889
D'Aquila Patrizia, Crocco Paolina, De Rango Francesco and 4 more
From surnames to linguistic and genetic diversity: five centuries of internal migrations in Spain.
Journal of anthropological sciences = Rivista di antropologia : JASS | 2017-12-30 | PMID 28885981
Rodríguez-Díaz Roberto, Blanco-Villegas María José, Manni Franz