Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia

by Bessho, K., Haga, H., Ikeno, M., Isobe, Y., Kiso, H., Koyama, N., Nakao, K., Shimizu, A., Sugai, M., Takahashi, K.
Published 2018

Primary failure of eruption: Clinical and genetic findings in the mixed dentition

by Cafiero, C., D'Apolito, I., Frazier-Bowers, S.A, Grippaudo, C., Ricci, B.
Published 2018

Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency

by Fang, Y., Feng, Q., Leng, S., Peng, J., Sheng, Z., Wang, S., Xu, S., Zhang, L., Zhang, X., Zhang, X., Zhang, Y.
Published 2021

Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)

by Bagherian, H., Ghadamyari, F., Ghasemi, F., Heidari, M.M, Khatami, M., Merat, S., Rejali, L., Zeinali, S.
Published 2021

Evaluation of photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients with defects in the EYS gene: a possible cost-effective cellular model for mechanism-ori...

by Aoi, N., Iwanami, M., Komuta, Y., Rai, D., Seko, Y., Takahashi, Y., Umezawa, A.
Published 2022

Collision tumors revealed by prospectively assessing subtype-defining molecular alterations in 904 individual prostate cancer foci

by Alnajar, H., Axcrona, K., Axcrona, U., Barbieri, C.E, Beg, S., Bhinder, B., Blattner-Johnson, M., Bogaard, M., Cai, P.Y, Calagua, C., Chinnaiyan, A.M, Croyle, J.A, Elemento, O., Fontugne, J., Johannessen, B., MacDonald, T.Y, Mosquera, J.M, Noorzad, Z., Park, K., Rubin, M.A, Sailer, V., Sanda, M.G, Scherr, D.S, Siddiqui, J., Skotheim, R.I, Ye, H.
Published 2022

A data-driven approach for constructing mutation categories for mutational signature analysis

by Gilad, G., Leiserson, M.D.M, Sharan, R.
Published 2021

VE1 immunohistochemistry is an adjunct tool for detection of BRAFV600E mutation: Validation in thyroid cancer patients

by Ansari, H.R, Asif, M., Khan, M.S, Rashid, F.A, Sameer Aga, S., Sheikh, A.K, Tabassum, S.
Published 2021

The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences

by Arveiler, B., Bagdonaite-Bejaran, L., Bergen, A.A, Birk, O.S, Blumenfeld, A., De Wit, G.C, Florijn, R.J, Fulton, A.B, Gradstein, L., Kruijt, C.C, Lasseaux, E., Perez, Y., Schalij-Delfos, N.E, Van Genderen, M.M, Yahalom, C., Zanlonghi, X.
Published 2022

Mitochondrial DNA mutations in Malaysian female breast cancer patients

by Abdullah, M.A, Ahmad, A.F, Ang, G.Y, Baghawi, A., Emran, N.A, Kitan, N., Maniam, S., Omasanggar, R., Teh, L.K, Yu, C.Y
Published 2020

Enhancement of the production of L-glutaminase, an anticancer enzyme, from Aeromonas veronii by adaptive and induced mutation techniques

by Aravinth Vijay Jesuraj, S., Marylin Jeya Praya, S., Ming, L.C, Moklesur Rahman Sarker, Md, Ravikumar, M., Wui, W.T
Published 2017

Mutational analysis of CYP2C8 in hypertensive patients using denaturing high performance liquid chromatography

by Ismail, R., Salleh, M.Z, Teh, L.K, Zahri, M.K, Zakaria, Z.A

Heterozygous familial hypercholesterolaemia in a pair of identical twins: A case report and updated review

by Al-Khateeb, A.M, Chua, Y.-A, Mohd Kasim, N.A, Mohd Nawawi, H., Mohd Nor, N.S
Published 2019

Factors associated with participation by African Americans in a study of the genetics of glaucoma

by Addis, V., Lehman, A., Maguire, M., Mccoskey, M., Miller-Ellis, E., O’Brien, J., O’Keefe, L., Pan, W., Parikh, R., Salowe, R., Sankar, P.
Published 2019