UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

Nature genetics, 2010-03, Vol.42 (3), p.229-233

2010

Volltextzugriff (PDF)

Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS

The journal of clinical endocrinology and metabolism, 2013-02, Vol.98 (2), p.E364-E369

2013

Volltextzugriff (PDF)

In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas

Endocrine-related cancer, 2013-06, Vol.20 (3), p.349-359

2013

Volltextzugriff (PDF)

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

JAMA : the journal of the American Medical Association, 2010-12, Vol.304 (23), p.2611

2010

Volltextzugriff (PDF)

Early‐onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1–associated primary hyperparathyroidism

Journal of bone and mineral research, 2010-11, Vol.25 (11), p.2382-2391

2010

Volltextzugriff (PDF)

Nomenclatural and taxonomic updates in Rourea subgen. Rourea sect. Multifoliolatae (Connaraceae)

PhytoKeys, 2020-12, Vol.169 (2), p.137-175

2020

Volltextzugriff (PDF)

Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma

The journal of clinical endocrinology and metabolism, 2007-05, Vol.92 (5), p.1934-1937

2007

Volltextzugriff (PDF)

Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma

Clinics (São Paulo, Brazil), 2009-01, Vol.64 (7), p.699-706

2009

Volltextzugriff (PDF)

Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study

The journal of clinical endocrinology and metabolism, 2010-11, Vol.95 (11), p.E373-E383

2010

Volltextzugriff (PDF)

Assessment of Depression, Anxiety, Quality of Life, and Coping in Long-Standing Multiple Endocrine Neoplasia Type 2 Patients

Thyroid (New York, N.Y.), 2017-05, Vol.27 (5), p.693-706

2017

Volltextzugriff (PDF)

Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile

European journal of endocrinology, 2008-09, Vol.159 (3), p.259-274

2008

Volltextzugriff (PDF)

Earthquake source parameters that display the first digit phenomenon

Nonlinear processes in geophysics, 2015-10, Vol.22 (5), p.625-632

2015

Volltextzugriff (PDF)

Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation

The journal of clinical endocrinology and metabolism, 2015-02, Vol.100 (2), p.E308-E318

2015

Volltextzugriff (PDF)

Penetrance of Functioning and Nonfunctioning Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 in the Second Decade of Life

The journal of clinical endocrinology and metabolism, 2014-01, Vol.99 (1), p.E89-E96

2014

Volltextzugriff (PDF)

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10

Human mutation, 2011-01, Vol.32 (1), p.51-58

2011

Volltextzugriff (PDF)

Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy

Clinical endocrinology (Oxford), 2010-04, Vol.72 (4), p.462-468

2010

Volltextzugriff (PDF)

Taxonomic revision of neotropical Connarus (Connaraceae) identifies three undescribed species

Willdenowia, 2021-06, Vol.51 (2)

2021

Volltextzugriff (PDF)

Out of Sight, Out of Mind: Widespread Nuclear and Plastid-Nuclear Discordance in the Flowering Plant Genus Polemonium (Polemoniaceae) Suggests Widespread Historical Gene Flow Despite Limited Nuclear Signal

Systematic biology, 2021-01, Vol.70 (1), p.162-180

2021

Volltextzugriff (PDF)

Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation

Pituitary, 2012-09, Vol.15 (3), p.342-349

2012

Volltextzugriff (PDF)

Surgical approach to medullary thyroid carcinoma associated with multiple endocrine neoplasia type 2

Clinics (São Paulo, Brazil), 2012-01, Vol.67 (Suppl 1), p.149-154

2012

Volltextzugriff (PDF)

A differential diagnosis of inherited endocrine tumors and their tumor counterparts

Clinics (São Paulo, Brazil), 2013-07, Vol.68 (7), p.1039-1056

2013

Volltextzugriff (PDF)

Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1

Clinics (São Paulo, Brazil), 2012-01, Vol.67 (suppl 1), p.99-108

2012

Volltextzugriff (PDF)

High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene

The journal of clinical endocrinology and metabolism, 2010-03, Vol.95 (3), p.1318-1327

2010

Volltextzugriff (PDF)

RET Y791F: alone or accompanied?

Archives of endocrinology and metabolism, 2015-10, Vol.59 (5), p.476-477

2015

Volltextzugriff (PDF)

1 – 25 von 3.505

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.855)
Mit Volltextzugriff
(2.873)

Publikationsform

4 weitere anzeigen...

Weniger anzeigen...

Sprache

5 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.066)
Life Sciences & Biomedicine
(1.328)
Humans
(865)
Female
(544)
Male
(516)
Physical Sciences
(461)
Technology
(395)
Animals
(362)
Biological And Medical Sciences
(307)
Adult
(297)
Middle Aged
(246)
Physics
(237)
Medical Sciences
(206)
Aged
(177)
Computer Science
(158)
Adolescent
(156)
Engineering
(147)
Fundamental And Applied Biological Sciences. Psychology
(135)
Chemistry
(131)
Child
(123)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

Free E-Journal (出版社公開部分のみ）
(1.604)
IngentaConnect
(1.538)
MEDLINE
(1.204)
Elsevier ScienceDirect Journals Complete
(713)
Journals@Ovid Full Text
(706)
IngentaConnect Journals
(607)
NUS Single-Journal Subscriptions
(465)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(432)
Wiley Online Library Journals Frontfile Complete
(346)
SpringerLink
(315)
Wiley Online Library
(230)
IEEE Electronic Library Online
(198)
Oxford Journals
(171)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(141)
JSTOR
(103)
Oxford Journals 2020 Medicine
(98)
Taylor & Francis Journals
(81)
Nature_系列刊
(78)
Ebook Central Perpetual and DDA
(77)
eBooks on EBSCOhost
(74)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS

In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

Early‐onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1–associated primary hyperparathyroidism

Nomenclatural and taxonomic updates in Rourea subgen. Rourea sect. Multifoliolatae (Connaraceae)

Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma

Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma

Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study

Assessment of Depression, Anxiety, Quality of Life, and Coping in Long-Standing Multiple Endocrine Neoplasia Type 2 Patients

Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile

Earthquake source parameters that display the first digit phenomenon

Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation

Penetrance of Functioning and Nonfunctioning Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 in the Second Decade of Life

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10

Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy

Taxonomic revision of neotropical Connarus (Connaraceae) identifies three undescribed species

Out of Sight, Out of Mind: Widespread Nuclear and Plastid-Nuclear Discordance in the Flowering Plant Genus Polemonium (Polemoniaceae) Suggests Widespread Historical Gene Flow Despite Limited Nuclear Signal

Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation

Surgical approach to medullary thyroid carcinoma associated with multiple endocrine neoplasia type 2

Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations

A differential diagnosis of inherited endocrine tumors and their tumor counterparts

Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1

High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene

RET Y791F: alone or accompanied?

Suchergebnisse filtern