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Best matches for Molecular pathogenesis of Jallmann's Syndrome:

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Items: 1 to 20 of 58368

  • The following term was not found in PubMed: Jallmann's.
1.

[Proteins from Vps13 family: from molecular function to pathogenesis of neurodegenerative disorders].

Kamińska J, Kolakowski D.

Postepy Biochem. 2018 Dec 29;64(4):275-287. Polish.

PMID:
30656912
2.

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.

Mann N, Braun DA, Amann K, Tan W, Shril S, Connaughton DM, Nakayama M, Schneider R, Kitzler TM, van der Ven AT, Chen J, Ityel H, Vivante A, Majmundar AJ, Daga A, Warejko JK, Lovric S, Ashraf S, Jobst-Schwan T, Widmeier E, Hugo H, Mane SM, Spaneas L, Somers MJG, Ferguson MA, Traum AZ, Stein DR, Baum MA, Daouk GH, Lifton RP, Manzi S, Vakili K, Kim HB, Rodig NM, Hildebrandt F.

J Am Soc Nephrol. 2019 Jan 17. pii: ASN.2018060575. doi: 10.1681/ASN.2018060575. [Epub ahead of print]

PMID:
30655312
3.

Genomic loss of HLA alleles may affect the clinical outcome in low-risk myelodysplastic syndrome patients.

Montes P, Kerick M, Bernal M, Hernández F, Jiménez P, Garrido P, Márquez A, Jurado M, Martin J, Garrido F, Ruiz-Cabello F.

Oncotarget. 2018 Dec 11;9(97):36929-36944. doi: 10.18632/oncotarget.26405. eCollection 2018 Dec 11.

4.

Molecular Pathways and Respiratory Involvement in Lysosomal Storage Diseases.

Faverio P, Stainer A, De Giacomi F, Gasperini S, Motta S, Canonico F, Pieruzzi F, Monzani A, Pesci A, Biondi A.

Int J Mol Sci. 2019 Jan 15;20(2). pii: E327. doi: 10.3390/ijms20020327. Review.

5.

Advances in MERS-CoV Vaccines and Therapeutics Based on the Receptor-Binding Domain.

Zhou Y, Yang Y, Huang J, Jiang S, Du L.

Viruses. 2019 Jan 14;11(1). pii: E60. doi: 10.3390/v11010060. Review.

6.

Juvenile transient bone marrow oedema of the foot associated with Vitamin D deficiency: A case study and an overview of pathogenesis and treatment.

Kaspiris A, Savvidou OD, Chrronopoulos E, Vasiliadis E.

Foot (Edinb). 2019 Jan 4;38:50-53. doi: 10.1016/j.foot.2019.01.002. [Epub ahead of print]

PMID:
30639799
7.

Disturbed redox homeostasis and oxidative stress: Potential players in the developmental regression in Rett syndrome.

Müller M.

Neurosci Biobehav Rev. 2019 Jan 9;98:154-163. doi: 10.1016/j.neubiorev.2018.12.009. [Epub ahead of print] Review.

PMID:
30639673
8.

The role of dietary non-heme iron load and peripheral nerve inflammation in the development of peripheral neuropathy (PN) in obese non-diabetic leptin-deficient ob/ob mice.

Kosacka J, Woidt K, Toyka KV, Paeschke S, Klöting N, Bechmann I, Blüher M, Thiery J, Ossmann S, Baum P, Nowicki M.

Neurol Res. 2019 Jan 13:1-13. doi: 10.1080/01616412.2018.1564191. [Epub ahead of print]

PMID:
30638160
9.

Phenotypic spectrum of NDE1-related disorders: from microlissencephaly to microhydranencephaly.

Abdel-Hamid MS, El-Dessouky SH, Ateya MI, Gaafar HM, Abdel-Salam GMH.

Am J Med Genet A. 2019 Jan 13. doi: 10.1002/ajmg.a.61035. [Epub ahead of print]

PMID:
30637988
10.

PrP 106-126 - 25 years after.

Forloni G, Chiesa R, Bugiani O, Salmona M, Tagliavini F.

Neuropathol Appl Neurobiol. 2019 Jan 12. doi: 10.1111/nan.12538. [Epub ahead of print] Review.

PMID:
30635947
11.

Betulinic acid alleviates endoplasmic reticulum stress-mediated NAFLD through activation of FXR in mice.

Gu M, Zhao P, Zhang S, Fan S, Yang L, Tong Q, Ji G, Huang C.

Br J Pharmacol. 2019 Jan 11. doi: 10.1111/bph.14570. [Epub ahead of print]

PMID:
30635917
12.

Genetic and transcriptional landscape of plasma cells in POEMS syndrome.

Nagao Y, Mimura N, Takeda J, Yoshida K, Shiozawa Y, Oshima M, Aoyama K, Saraya A, Koide S, Rizq O, Hasegawa Y, Shiraishi Y, Chiba K, Tanaka H, Nishijima D, Isshiki Y, Kayamori K, Kawajiri-Manako C, Oshima-Hasegawa N, Tsukamoto S, Mitsukawa S, Takeda Y, Ohwada C, Takeuchi M, Iseki T, Misawa S, Miyano S, Ohara O, Yokote K, Sakaida E, Kuwabara S, Sanada M, Iwama A, Ogawa S, Nakaseko C.

Leukemia. 2019 Jan 11. doi: 10.1038/s41375-018-0348-x. [Epub ahead of print]

PMID:
30635632
13.

Leukoencephalopathy due to variants in GFPT1-associated congenital myasthenic syndrome.

Helman G, Sharma S, Crawford J, Patra B, Jain P, Bent SJ, Urtizberea JA, Saran RK, Taft RJ, van der Knaap MS, Simons C.

Neurology. 2019 Jan 11. pii: 10.1212/WNL.0000000000006886. doi: 10.1212/WNL.0000000000006886. [Epub ahead of print]

PMID:
30635494
14.

Phospholipase Cε plays a crucial role in neutrophilic inflammation accompanying acute lung injury through augmentation of CXC chemokine production from alveolar epithelial cells.

Umezawa K, Nagano T, Kobayashi K, Dokuni R, Katsurada M, Yamamoto M, Yoshikawa Y, Kataoka T, Nishimura Y.

Respir Res. 2019 Jan 11;20(1):9. doi: 10.1186/s12931-019-0975-4.

15.

Contribution of FoxP3+ Tfr cells to overall human blood CXCR5+ T cells.

Fonseca VR, Graca L.

Clin Exp Immunol. 2019 Jan 10. doi: 10.1111/cei.13245. [Epub ahead of print]

PMID:
30632146
16.

Influenza B virus infection complicated by life-threatening pericarditis: a unique case-report and literature review.

Spoto S, Valeriani E, Locorriere L, Anguissola GB, Pantano AL, Terracciani F, Riva E, Ciccozzi M, Costantino S, Angeletti S.

BMC Infect Dis. 2019 Jan 10;19(1):40. doi: 10.1186/s12879-018-3606-7.

17.

Recent advances in Lynch syndrome.

Biller LH, Syngal S, Yurgelun MB.

Fam Cancer. 2019 Jan 9. doi: 10.1007/s10689-018-00117-1. [Epub ahead of print]

PMID:
30627969
18.

The biological function of ELABELA and APJ signaling in the cardiovascular system and pre-eclampsia.

Liu Y, Wang L, Shi H.

Hypertens Res. 2019 Jan 9. doi: 10.1038/s41440-018-0193-3. [Epub ahead of print] Review.

PMID:
30626933
19.

Organoid single cell profiling identifies a transcriptional signature of glomerular disease.

Harder JL, Menon R, Otto EA, Zhou J, Eddy S, Wys NL, O'Connor C, Luo J, Nair V, Cebrian C, Spence JR, Bitzer M, Troyanskaya OG, Hodgin JB, Wiggins RC, Freedman BS, Kretzler M; European Renal cDNA Bank (ERCB); Nephrotic Syndrome Study Network (NEPTUNE).

JCI Insight. 2019 Jan 10;4(1). pii: 122697. doi: 10.1172/jci.insight.122697. [Epub ahead of print]

20.

Plerixafor for the Treatment of WHIM Syndrome.

McDermott DH, Pastrana DV, Calvo KR, Pittaluga S, Velez D, Cho E, Liu Q, Trout HH 3rd, Neves JF, Gardner PJ, Bianchi DA, Blair EA, Landon EM, Silva SL, Buck CB, Murphy PM.

N Engl J Med. 2019 Jan 10;380(2):163-170. doi: 10.1056/NEJMoa1808575.

PMID:
30625055

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