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Items: 1 to 50 of 164

1.

Functional analysis of mammalian phospholipase D enzymes.

Panda A, Thakur R, Krishnan H, Naik A, Shinde D, Raghu P.

Biosci Rep. 2018 Oct 28. pii: BSR20181690. doi: 10.1042/BSR20181690. [Epub ahead of print]

PMID:
30369483
2.

Crystalline 2D Covalent Organic Framework Membranes for High-Flux Organic Solvent Nanofiltration.

Shinde DB, Sheng G, Li X, Ostwal M, Emwas AH, Huang KW, Lai Z.

J Am Chem Soc. 2018 Oct 31;140(43):14342-14349. doi: 10.1021/jacs.8b08788. Epub 2018 Oct 17.

PMID:
30289708
3.

In Situ Dynamic Nanostructuring of the Cu-Ti Catalyst-Support System Promotes Hydrogen Evolution under Alkaline Conditions.

Shinde DV, Dang Z, Petralanda U, Palei M, Wang M, Prato M, Cavalli A, De Trizio L, Manna L.

ACS Appl Mater Interfaces. 2018 Sep 5;10(35):29583-29592. doi: 10.1021/acsami.8b09493. Epub 2018 Aug 24.

PMID:
30088758
4.

Regulation of PI4P levels by PI4KIIIα during G-protein-coupled PLC signaling in Drosophila photoreceptors.

Balakrishnan SS, Basu U, Shinde D, Thakur R, Jaiswal M, Raghu P.

J Cell Sci. 2018 Aug 3;131(15). pii: jcs217257. doi: 10.1242/jcs.217257.

PMID:
29980590
5.

Unravelling the Nucleophilicity of Butenolides for 1,6-Conjugate Addition to p-Quinone Methides: A Direct Access to Diversely Substituted Butenolide-Derived Diarylmethanes.

Sharma BM, Shinde DR, Jain R, Begari E, Satbhaiya S, Gonnade RG, Kumar P.

Org Lett. 2018 May 4;20(9):2787-2791. doi: 10.1021/acs.orglett.8b00745. Epub 2018 Apr 26.

PMID:
29697260
6.

Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood.

Vögtle FN, Brändl B, Larson A, Pendziwiat M, Friederich MW, White SM, Basinger A, Kücükköse C, Muhle H, Jähn JA, Keminer O, Helbig KL, Delto CF, Myketin L, Mossmann D, Burger N, Miyake N, Burnett A, van Baalen A, Lovell MA, Matsumoto N, Walsh M, Yu HC, Shinde DN, Stephani U, Van Hove JLK, Müller FJ, Helbig I.

Am J Hum Genet. 2018 Apr 5;102(4):557-573. doi: 10.1016/j.ajhg.2018.02.014. Epub 2018 Mar 22.

7.

Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.

Peng Y, Shinde DN, Alexander Valencia C, Mo JS, Rosenfeld J, Cho MT, Chamberlin A, Li Z, Liu J, Gui B.

Hum Mol Genet. 2018 Jun 15;27(12):2224. doi: 10.1093/hmg/ddy072. No abstract available.

8.

Iron Catalyzed Hydroformylation of Alkenes under Mild Conditions: Evidence of an Fe(II) Catalyzed Process.

Pandey S, Raj KV, Shinde DR, Vanka K, Kashyap V, Kurungot S, Vinod CP, Chikkali SH.

J Am Chem Soc. 2018 Mar 28;140(12):4430-4439. doi: 10.1021/jacs.8b01286. Epub 2018 Mar 19.

PMID:
29526081
9.

Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases.

Farwell Hagman KD, Shinde DN, Mroske C, Smith E, Radtke K, Shahmirzadi L, El-Khechen D, Powis Z, Chao EC, Alcaraz WA, Helbig KL, Sajan SA, Rossi M, Lu HM, Huether R, Li S, Wu S, Nuñes ME, Tang S.

Genet Med. 2018 Sep;20(9):1099-1102. doi: 10.1038/gim.2017.263.

PMID:
29388939
10.

Biallelic Mutations in FUT8 Cause a Congenital Disorder of Glycosylation with Defective Fucosylation.

Ng BG, Xu G, Chandy N, Steyermark J, Shinde DN, Radtke K, Raymond K, Lebrilla CB, AlAsmari A, Suchy SF, Powis Z, Faqeih EA, Berry SA, Kronn DF, Freeze HH.

Am J Hum Genet. 2018 Jan 4;102(1):188-195. doi: 10.1016/j.ajhg.2017.12.009.

11.

Microwave-assisted synthesis of novel 5-substituted benzylidene amino-2-butyl benzofuran-3-yl-4-methoxyphenyl methanones as antileishmanial and antioxidant agents.

Patil SR, Bollikonda S, Patil RH, Sangshetti JN, Bobade AS, Asrondkar A, Reddy PP, Shinde DB.

Bioorg Med Chem Lett. 2017 Dec 8. pii: S0960-894X(17)31173-3. doi: 10.1016/j.bmcl.2017.12.013. [Epub ahead of print]

PMID:
29258770
12.

De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms.

Powis Z, Petrik I, Cohen JS, Escolar D, Burton J, van Ravenswaaij-Arts CMA, Sival DA, Stegmann APA, Kleefstra T, Pfundt R, Chikarmane R, Begtrup A, Huether R, Tang S, Shinde DN.

Clin Genet. 2018 May;93(5):1030-1038. doi: 10.1111/cge.13198. Epub 2018 Jan 25.

PMID:
29251763
13.

De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities.

Martin S, Chamberlin A, Shinde DN, Hempel M, Strom TM, Schreiber A, Johannsen J, Ousager LB, Larsen MJ, Hansen LK, Fatemi A, Cohen JS, Lemke J, Sørensen KP, Helbig KL, Lessel D, Abou Jamra R.

Am J Hum Genet. 2017 Dec 7;101(6):1013-1020. doi: 10.1016/j.ajhg.2017.11.004.

14.

A modular approach towards functionalized highly stable self-complementary quadruple hydrogen bonded systems.

Rayavarapu S, Kheria S, Shinde DR, Gonnade RG, Sanjayan GJ.

Org Biomol Chem. 2017 Dec 6;15(47):10087-10094. doi: 10.1039/c7ob02358h.

PMID:
29170774
15.

Novel 2-(nitrooxy)ethyl 2-(4-(substituted phenyl)-2-((substituted phenyl)amino)thiazol-5-yl)acetate as Anti-inflammatory, Analgesic and Nitric Oxide Releasing Agents: Synthesis and Molecular Docking Studies.

Sarkate AP, Lokwani DK, Karnik KS, Shinde DB.

Antiinflamm Antiallergy Agents Med Chem. 2017;16(3):153-167. doi: 10.2174/1871523016666171115125922.

PMID:
29141568
16.

Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.

Peng Y, Shinde DN, Valencia CA, Mo JS, Rosenfeld J, Truitt Cho M, Chamberlin A, Li Z, Liu J, Gui B, Brockhage R, Basinger A, Alvarez-Leon B, Heydemann P, Magoulas PL, Lewis AM, Scaglia F, Gril S, Chong SC, Bower M, Monaghan KG, Willaert R, Plona MR, Dineen R, Milan F, Hoganson G, Powis Z, Helbig KL, Keller-Ramey J, Harris B, Anderson LC, Green T, Sukoff Rizzo SJ, Kaylor J, Chen J, Guan MX, Sellars E, Sparagana SP, Gibson JB, Reinholdt LG, Tang S, Huang T.

Hum Mol Genet. 2017 Dec 15;26(24):4937-4950. doi: 10.1093/hmg/ddx377.

17.

Self-assembly of P-chiral supramolecular phosphines on rhodium and direct evidence for Rh-catalyst-substrate interactions.

Koshti VS, Sen A, Shinde D, Chikkali SH.

Dalton Trans. 2017 Oct 17;46(40):13966-13973. doi: 10.1039/c7dt02923c.

PMID:
28972617
18.

H-Bonding Assisted Self-Assembly of Anionic and Neutral Ligand on Metal: A Comprehensive Strategy To Mimic Ditopic Ligands in Olefin Polymerization.

Mote NR, Patel K, Shinde DR, Gaikwad SR, Koshti VS, Gonnade RG, Chikkali SH.

Inorg Chem. 2017 Oct 16;56(20):12448-12456. doi: 10.1021/acs.inorgchem.7b01923. Epub 2017 Sep 28.

PMID:
28956911
19.

De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with Seizures.

Myers CT, Stong N, Mountier EI, Helbig KL, Freytag S, Sullivan JE, Ben Zeev B, Nissenkorn A, Tzadok M, Heimer G, Shinde DN, Rezazadeh A, Regan BM, Oliver KL, Ernst ME, Lippa NC, Mulhern MS, Ren Z, Poduri A, Andrade DM, Bird LM, Bahlo M, Berkovic SF, Lowenstein DH, Scheffer IE, Sadleir LG, Goldstein DB, Mefford HC, Heinzen EL.

Am J Hum Genet. 2017 Oct 5;101(4):516-524. doi: 10.1016/j.ajhg.2017.08.013. Epub 2017 Sep 21.

20.

Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features.

Stankiewicz P, Khan TN, Szafranski P, Slattery L, Streff H, Vetrini F, Bernstein JA, Brown CW, Rosenfeld JA, Rednam S, Scollon S, Bergstrom KL, Parsons DW, Plon SE, Vieira MW, Quaio CRDC, Baratela WAR, Acosta Guio JC, Armstrong R, Mehta SG, Rump P, Pfundt R, Lewandowski R, Fernandes EM, Shinde DN, Tang S, Hoyer J, Zweier C, Reis A, Bacino CA, Xiao R, Breman AM, Smith JL; Deciphering Developmental Disorders Study, Katsanis N, Bostwick B, Popp B, Davis EE, Yang Y.

Am J Hum Genet. 2017 Oct 5;101(4):503-515. doi: 10.1016/j.ajhg.2017.08.014. Epub 2017 Sep 21.

21.

Antileishmanial potential of fused 5-(pyrazin-2-yl)-4H-1,2,4-triazole-3-thiols: Synthesis, biological evaluations and computational studies.

Patil SR, Asrondkar A, Patil V, Sangshetti JN, Kalam Khan FA, Damale MG, Patil RH, Bobade AS, Shinde DB.

Bioorg Med Chem Lett. 2017 Aug 15;27(16):3845-3850. doi: 10.1016/j.bmcl.2017.06.053. Epub 2017 Jun 22.

PMID:
28693910
22.

DNM1 encephalopathy: A new disease of vesicle fission.

von Spiczak S, Helbig KL, Shinde DN, Huether R, Pendziwiat M, Lourenço C, Nunes ME, Sarco DP, Kaplan RA, Dlugos DJ, Kirsch H, Slavotinek A, Cilio MR, Cervenka MC, Cohen JS, McClellan R, Fatemi A, Yuen A, Sagawa Y, Littlejohn R, McLean SD, Hernandez-Hernandez L, Maher B, Møller RS, Palmer E, Lawson JA, Campbell CA, Joshi CN, Kolbe DL, Hollingsworth G, Neubauer BA, Muhle H, Stephani U, Scheffer IE, Pena SDJ, Sisodiya SM, Helbig I; Epi4K Consortium; EuroEPINOMICS-RES NLES Working Group.

Neurology. 2017 Jul 25;89(4):385-394. doi: 10.1212/WNL.0000000000004152. Epub 2017 Jun 30.

23.

Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy.

Theisen BE, Rumyantseva A, Cohen JS, Alcaraz WA, Shinde DN, Tang S, Srivastava S, Pevsner J, Trifunovic A, Fatemi A.

Am J Med Genet A. 2017 Sep;173(9):2505-2510. doi: 10.1002/ajmg.a.38339. Epub 2017 Jun 26.

PMID:
28650581
24.

Coumarin-Appended Stable Fluorescent Self-Complementary Quadruple-Hydrogen-Bonded Molecular Duplexes.

Kheria S, Rayavarapu S, Kotmale AS, Shinde DR, Gonnade RG, Sanjayan GJ.

J Org Chem. 2017 Jun 16;82(12):6403-6408. doi: 10.1021/acs.joc.7b01249. Epub 2017 Jun 6.

PMID:
28558211
25.

Crystallisation-enhanced bulk hole mobility in phenothiazine-based organic semiconductors.

Shinde DB, Salunke JK, Candeias NR, Tinti F, Gazzano M, Wadgaonkar PP, Priimagi A, Camaioni N, Vivo P.

Sci Rep. 2017 Apr 12;7:46268. doi: 10.1038/srep46268.

26.

Secondary Interactions Arrest the Hemiaminal Intermediate To Invert the Modus Operandi of Schiff Base Reaction: A Route to Benzoxazinones.

Patel K, Deshmukh SS, Bodkhe D, Mane M, Vanka K, Shinde D, Rajamohanan PR, Nandi S, Vaidhyanathan R, Chikkali SH.

J Org Chem. 2017 Apr 21;82(8):4342-4351. doi: 10.1021/acs.joc.7b00352. Epub 2017 Apr 11.

PMID:
28378576
27.

Enhanced Efficiency and Stability of an Aqueous Lead-Nitrate-Based Organometallic Perovskite Solar Cell.

Shinde DV, Pyeon L, Pei M, Kim GW, Yang H, Park T.

ACS Appl Mater Interfaces. 2017 Apr 26;9(16):14023-14030. doi: 10.1021/acsami.7b01864. Epub 2017 Apr 11.

PMID:
28361530
28.

Mur Ligase Inhibitors as Anti-bacterials: A Comprehensive Review.

Sangshetti JN, Joshi SS, Patil RH, Moloney MG, Shinde DB.

Curr Pharm Des. 2017;23(21):3164-3196. doi: 10.2174/1381612823666170214115048. Review.

PMID:
28201974
29.

Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications.

Smith ED, Radtke K, Rossi M, Shinde DN, Darabi S, El-Khechen D, Powis Z, Helbig K, Waller K, Grange DK, Tang S, Farwell Hagman KD.

Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.

30.

Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides.

Bagle PN, Mane MV, Vanka K, Shinde DR, Shaikh SR, Gonnade RG, Patil NT.

Chem Commun (Camb). 2016 Dec 13;52(100):14462-14465.

PMID:
27901528
31.

Bacterial Peptide Deformylase Inhibition of Tetrazole-Substituted Biaryl Acid Analogs: Synthesis, Biological Evaluations, and Molecular Docking Study.

Khan FA, Patil RH, Patil M, Arote R, Shinde DB, Sangshetti JN.

Arch Pharm (Weinheim). 2016 Dec;349(12):934-943. doi: 10.1002/ardp.201600254. Epub 2016 Nov 16.

PMID:
27859538
32.

Design and synthesis of 4'-((5-benzylidene-2,4-dioxothiazolidin-3-yl)methyl)biphenyl-2-carbonitrile analogs as bacterial peptide deformylase inhibitors.

Khan FA, Patil RH, Shinde DB, Sangshetti JN.

Chem Biol Drug Des. 2016 Dec;88(6):938-944. doi: 10.1111/cbdd.12817. Epub 2016 Aug 17.

PMID:
27401234
33.

Biphenyl tetrazole-thiazolidinediones as novel bacterial peptide deformylase inhibitors: Synthesis, biological evaluations and molecular docking study.

Khan FAK, Jadhav KS, Patil RH, Shinde DB, Arote RB, Sangshetti JN.

Biomed Pharmacother. 2016 Oct;83:1146-1153. doi: 10.1016/j.biopha.2016.08.036. Epub 2016 Aug 20.

PMID:
27551762
34.

Expedient Cobalt-Catalyzed C-H Alkynylation of (Enantiopure) Benzylamines.

Landge VG, Midya SP, Rana J, Shinde DR, Balaraman E.

Org Lett. 2016 Oct 4. [Epub ahead of print]

PMID:
27700123
35.

Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features.

Cohen JS, Srivastava S, Farwell Hagman KD, Shinde DN, Huether R, Darcy D, Wallerstein R, Houge G, Berland S, Monaghan KG, Poretti A, Wilson AL, Chung WK, Fatemi A.

Clin Genet. 2017 May;91(5):697-707. doi: 10.1111/cge.12861. Epub 2016 Oct 10.

PMID:
27598823
36.

De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.

Kim JH, Shinde DN, Reijnders MRF, Hauser NS, Belmonte RL, Wilson GR, Bosch DGM, Bubulya PA, Shashi V, Petrovski S, Stone JK, Park EY, Veltman JA, Sinnema M, Stumpel CTRM, Draaisma JM, Nicolai J; University of Washington Center for Mendelian Genomics, Yntema HG, Lindstrom K, de Vries BBA, Jewett T, Santoro SL, Vogt J; Deciphering Developmental Disorders Study, Bachman KK, Seeley AH, Krokosky A, Turner C, Rohena L, Hempel M, Kortüm F, Lessel D, Neu A, Strom TM, Wieczorek D, Bramswig N, Laccone FA, Behunova J, Rehder H, Gordon CT, Rio M, Romana S, Tang S, El-Khechen D, Cho MT, McWalter K, Douglas G, Baskin B, Begtrup A, Funari T, Schoch K, Stegmann APA, Stevens SJC, Zhang DE, Traver D, Yao X, MacArthur DG, Brunner HG, Mancini GM, Myers RM, Owen LB, Lim ST, Stachura DL, Vissers LELM, Ahn EYE.

Am J Hum Genet. 2016 Sep 1;99(3):711-719. doi: 10.1016/j.ajhg.2016.06.029. Epub 2016 Aug 18.

37.

A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.

Helbig KL, Hedrich UB, Shinde DN, Krey I, Teichmann AC, Hentschel J, Schubert J, Chamberlin AC, Huether R, Lu HM, Alcaraz WA, Tang S, Jungbluth C, Dugan SL, Vainionpää L, Karle KN, Synofzik M, Schöls L, Schüle R, Lehesjoki AE, Helbig I, Lerche H, Lemke JR.

Ann Neurol. 2016 Oct;80(4). doi: 10.1002/ana.24762. Epub 2016 Sep 9.

38.

Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases.

Farwell Hagman KD, Shinde DN, Mroske C, Smith E, Radtke K, Shahmirzadi L, El-Khechen D, Powis Z, Chao EC, Alcaraz WA, Helbig KL, Sajan SA, Rossi M, Lu HM, Huether R, Li S, Wu S, Nuñes ME, Tang S.

Genet Med. 2017 Feb;19(2):224-235. doi: 10.1038/gim.2016.95. Epub 2016 Aug 11. Erratum in: Genet Med. 2018 Feb 01;:.

39.

Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy.

Rudolf G, Lesca G, Mehrjouy MM, Labalme A, Salmi M, Bache I, Bruneau N, Pendziwiat M, Fluss J, de Bellescize J, Scholly J, Møller RS, Craiu D, Tommerup N, Valenti-Hirsch MP, Schluth-Bolard C, Sloan-Béna F, Helbig KL, Weckhuysen S, Edery P, Coulbaut S, Abbas M, Scheffer IE, Tang S, Myers CT, Stamberger H, Carvill GL, Shinde DN, Mefford HC, Neagu E, Huether R, Lu HM, Dica A, Cohen JS, Iliescu C, Pomeran C, Rubenstein J, Helbig I, Sanlaville D, Hirsch E, Szepetowski P.

Eur J Hum Genet. 2016 Dec;24(12):1761-1770. doi: 10.1038/ejhg.2016.80. Epub 2016 Jun 29.

40.

Fabrication of carbon nanorods and graphene nanoribbons from a metal-organic framework.

Pachfule P, Shinde D, Majumder M, Xu Q.

Nat Chem. 2016 Jul;8(7):718-24. doi: 10.1038/nchem.2515. Epub 2016 May 9.

PMID:
27325100
41.

Synthesis and antimicrobial evaluation of novel ethyl 2-(2-(4-substituted)acetamido)-4-subtituted-thiazole-5-carboxylate derivatives.

Pawar CD, Sarkate AP, Karnik KS, Bahekar SS, Pansare DN, Shelke RN, Jawale CS, Shinde DB.

Bioorg Med Chem Lett. 2016 Aug 1;26(15):3525-8. doi: 10.1016/j.bmcl.2016.06.030. Epub 2016 Jun 11.

PMID:
27324976
42.

Bacterial Peptide deformylase inhibition of cyano substituted biaryl analogs: Synthesis, in vitro biological evaluation, molecular docking study and in silico ADME prediction.

Khan FA, Patil RH, Shinde DB, Sangshetti JN.

Bioorg Med Chem. 2016 Aug 15;24(16):3456-63. doi: 10.1016/j.bmc.2016.05.051. Epub 2016 May 28.

PMID:
27269198
43.

Shear Assisted Electrochemical Exfoliation of Graphite to Graphene.

Shinde DB, Brenker J, Easton CD, Tabor RF, Neild A, Majumder M.

Langmuir. 2016 Apr 12;32(14):3552-9. doi: 10.1021/acs.langmuir.5b04209. Epub 2016 Apr 4.

PMID:
27043919
44.

Large-area graphene-based nanofiltration membranes by shear alignment of discotic nematic liquid crystals of graphene oxide.

Akbari A, Sheath P, Martin ST, Shinde DB, Shaibani M, Banerjee PC, Tkacz R, Bhattacharyya D, Majumder M.

Nat Commun. 2016 Mar 7;7:10891. doi: 10.1038/ncomms10891.

45.

Gold vs Rhodium Catalysis: Tuning Reactivity through Catalyst Control in the C-H Alkynylation of Isoquinolones.

Shaikh AC, Shinde DR, Patil NT.

Org Lett. 2016 Mar 4;18(5):1056-9. doi: 10.1021/acs.orglett.6b00175. Epub 2016 Feb 17.

PMID:
26886569
46.

Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.

Helbig KL, Farwell Hagman KD, Shinde DN, Mroske C, Powis Z, Li S, Tang S, Helbig I.

Genet Med. 2016 Sep;18(9):898-905. doi: 10.1038/gim.2015.186. Epub 2016 Jan 21.

PMID:
26795593
47.

Antileishmanial activity of novel indolyl-coumarin hybrids: Design, synthesis, biological evaluation, molecular docking study and in silico ADME prediction.

Sangshetti JN, Kalam Khan FA, Kulkarni AA, Patil RH, Pachpinde AM, Lohar KS, Shinde DB.

Bioorg Med Chem Lett. 2016 Feb 1;26(3):829-835. doi: 10.1016/j.bmcl.2015.12.085. Epub 2015 Dec 24.

PMID:
26778149
48.

Design of selective TACE inhibitors using molecular docking studies: Synthesis and preliminary evaluation of anti-inflammatory and TACE inhibitory activity.

Sarkate AP, Murumkar PR, Lokwani DK, Kandhare AD, Bodhankar SL, Shinde DB, Bothara KG.

SAR QSAR Environ Res. 2015;26(11):905-23. doi: 10.1080/1062936X.2015.1095240.

PMID:
26588187
49.

Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalities.

Mroske C, Rasmussen K, Shinde DN, Huether R, Powis Z, Lu HM, Baxter RM, McPherson E, Tang S.

BMC Med Genet. 2015 Nov 5;16:102. doi: 10.1186/s12881-015-0240-8.

50.

Recall Rate Reduction with Tomosynthesis During Baseline Screening Examinations: An Assessment From a Prospective Trial.

Sumkin JH, Ganott MA, Chough DM, Catullo VJ, Zuley ML, Shinde DD, Hakim CM, Bandos AI, Gur D.

Acad Radiol. 2015 Dec;22(12):1477-82. doi: 10.1016/j.acra.2015.08.015. Epub 2015 Sep 26.

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