Results 141 to 150 of about 18,144 (235)

Identification of potentially deleterious mutations in gastric cancer using patient-derived xenograft models. [PDF]

Front Genet
Kong L, Wang J, Zheng J, Yang X, Sun R, Kou J, Yao Y, Li F, Wang F, Guo S.   +9 more
europepmc   +1 more source

Sustainability of remote communities: 100% renewable island of Hvar [PDF]

, 2013
Aalborg University, Boris Ćosić, Neven Duić, Zlatko Bačelić Medić   +3 more
core   +1 more source

Assessing the performance of 28 pathogenicity prediction methods on rare single nucleotide variants in coding regions. [PDF]

BMC Genomics
Heo JY, Kim JH.
europepmc   +1 more source

Archaeological research of a Roman villa in Soline Bay on the island of St. Clement (Pakleni Islands, Hvar) in June 2017

, 2015
Marina Ugarković, Ivančica Schrunk, Vlasta Begović, Marinko Petrić   +3 more
openalex  

Diabetes mellitus <i>HNF4A</i>-MODY in children from the Russian population: clinical and genetic features. [PDF]

Front Endocrinol (Lausanne)
Sechko EA, Laptev DN, Koltakova MP, Khusainova RI, Minniakhmetov IR, Kuraeva TL, Eremina IA, Titovich EV, Bezlepkina OB, Peterkova VA.   +9 more
europepmc   +1 more source

B-cell immunodeficiency associated with polynucleotide kinase 3'-phosphatase (PNKP) deficiency. [PDF]

J Allergy Clin Immunol Glob
Takada S, Okano T, Tanita K, Tsukada K, Watanabe M, Hijikata A, Naruto T, Yeh TW, Kasuga S, Tokimasa S, Taniguchi-Ikeda M, Ogata R, Ikeda A, Goto T, Osaka H, Takagi M, Imai K, Morio T, van der Burg M, Shimada M, Kanegane H.   +20 more
europepmc   +1 more source

Clinical Trial on the Usefulness of an Intensive Low-Density Lipoprotein Cholesterol Treatment and Familial Hypercholesterolemia Screening Clinical Pathway for Acute Coronary Syndrome: The Hokuriku-plus Acute Coronary Syndrome Registry Study　- Rationale and Study Design. [PDF]

Circ Rep
Tada H, Takeji Y, Goten C, Inoue O, Okada H, Yoshida S, Shimojima M, Nomura A, Mori M, Takashima SI, Kato T, Usui S, Sakata K, Hayashi K, Fujino N, Toyama T, Miyagi S, Nagase K, Mizukoshi E, Miwa K, Yoshida T, Higashikata T, Noji Y, Takata M, Fujioka K, Nakahashi T, Otowa K, Mukai Y, Aburadani I, Takatori O, Ohtani K, Omi W, Takamura M.   +32 more
europepmc   +1 more source

Biallelic Variants in COQ4 Cause Childhood-Onset Pure Hereditary Spastic Paraplegia. [PDF]

Mov Disord Clin Pract
Schierbaum L, Quiroz V, Tam A, Zubair U, Tochen L, Srouji R, Yang K, Ebrahimi-Fakhari D.   +7 more
europepmc   +1 more source

Rare variant analyses provide insights into the genetic architecture of endometriosis. [PDF]

Hum Genomics
Gui Y, Xie Y, Tong X, Zhao H.
europepmc   +1 more source