Results 121 to 130 of about 13,672 (168)

Cell-type-specific alternative splicing in the brain and kidney of a Setbp1S858R Schinzel-Giedion syndrome mouse.

Dis Model Mech
Soelter TM, Jones EF, Howton TC, Crumley AB, Wilk EJ, Lasseigne BN.   +5 more
europepmc   +1 more source

Decoding Glioblastoma Through Liquid Biopsy: Molecular Insights and Clinical Prospects. [PDF]

Cells
Wasiak T, Jaskólska M, Filiks K, Bartkowiak J, Rutkowska A.   +4 more
europepmc   +1 more source

Diagnosis and Treatment of Iron Deficiency and Iron Deficiency Anemia in Children and Adolescents: Recommendations of the Polish Pediatric Society, the Polish Society of Pediatric Oncology and Hematology, the Polish Society of Neonatology, and the Polish Society of Family Medicine. [PDF]

Nutrients
Chaber R, Helwich E, Lauterbach R, Mastalerz-Migas A, Matysiak M, Peregud-Pogorzelski J, Styczyński J, Szczepański T, Jackowska T.   +8 more
europepmc   +1 more source

The spatial analysis of multimorbidity in Thai Cohort Study. [PDF]

Arch Public Health
Feng X, Sarma H, Bagheri N, Tsheten T, Seubsman SA, Sleigh A, Kelly M.   +6 more
europepmc   +1 more source

Rare disease publishing trends worldwide and in China: A CiteSpace-based bibliometric study. [PDF]

Intractable Rare Dis Res
Kong Q, Fan C, Zhang Y, Yan X, Chen L, Kang Q, Yin P.   +6 more
europepmc   +1 more source

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations. [PDF]

Nat Commun
Kobren SN, Moldovan MA, Reimers R, Traviglia D, Li X, Barnum D, Veit A, Corona RI, Carvalho Neto GV, Willett J, Berselli M, Ronchetti W, Nelson SF, Martinez-Agosto JA, Sherwood R, Krier J, Kohane IS, Undiagnosed Diseases Network, Sunyaev SR.   +18 more
europepmc   +1 more source

Investigation of Profile-Related Evidence Determining Individualized Cancer Therapy (I-PREDICT) N-of-1 Precision Oncology Study: Molecular Profiling to Match Individually Dosed, Personalized Drug Combinations. [PDF]

J Clin Oncol
Sicklick JK, Nishizaki D, Miyashita H, Okamura R, Hahn ME, Nikanjam M, Fanta PT, Piccioni DE, Patel H, Eskander RN, McKay RR, Ross JS, Lee JJ, Lippman SM, Kato S, Kurzrock R.   +15 more
europepmc   +1 more source

Contemporary intergeneric hybridization and backcrossing among birds-of-paradise. [PDF]

Evol Lett
Thörn F, Soares AER, Müller IA, Päckert M, Frahnert S, van Grouw H, Kamminga P, Peona V, Suh A, Blom MPK, Irestedt M.   +10 more
europepmc   +1 more source

Insights from multidisciplinary rare disease visits: Findings from wrap-up documents and participant surveys in a national diagnostic study. [PDF]

Rare
Rosenfeld LE, LeBlanc K, Nagy A, Bater J, Undiagnosed Diseases Network, McCray AT.   +5 more
europepmc   +1 more source

Privacy-by-Design Approach to Generate Two Virtual Clinical Trials for Multiple Sclerosis and Release Them as Open Datasets: Evaluation Study.

J Med Internet Res
Demuth S, Rousseau O, Faddeenkov I, Paris J, De Sèze J, Baciotti B, Payet M, Guillaudeux M, Barreteau AF, Laplaud D, Edan G, Gourraud PA.   +11 more
europepmc   +1 more source